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Dedication
Contributors
Foreword
Christine Craik
Foreword
John Glossop
Preface
Chapter 1
Overview of client-centred practice
T. Sumsion
CHAPTER CONTENTS
Emerging importance of client-centred Outcomes and effectiveness 8
practice 1 Model of Occupational Performance 9
Models of client-centred practice 3 Relationship of the Model of Occupational
Definitions 5 Performance to other approaches 15
Client-centred programmes 7 Conclusion 16
health care and to be responsible for their own health. Health promotion,
as defined by the World Health Organization, is ‘the process of enabling
people to increase control over and to improve their health’ (WHO 1986,
p 1). The recognition of the importance of these concepts has facilitated
their integration into many programmes that fully support consumer
awareness. Further developments in the 1990s and beyond have seen
the emergence of consumer-led and self-help groups which strive to
meet needs outside the realm of professional involvement. These are truly
client-centred programmes. Consumer rights, human rights and the tech-
nological revolution have also hastened the development of client-centred
practice (Gage 1994, Law et al 1995).
Therapists in the United Kingdom are aware that the College of Occu-
pational Therapists supports the client-centred approach to intervention
by encouraging the involvement of the client as a partner in all stages of
the therapeutic process and stating within the Code of Ethics and Profes-
sional Conduct that services should be client-centred and needs led. This
document also reminds therapists that clients are unique and bring their
own perspective to the occupational therapy process (College of Occupa-
tional Therapists 2000). The Code of Ethics of the Canadian Association
of Occupational Therapists (CAOT) also advises members to demonstrate
respect for and appreciate the particular needs of the client (CAOT 1996).
It is important that therapists understand the implications of these state-
ments and have the necessary information to implement this approach.
Universities are also acknowledging the need to change the way future
therapists and doctors are educated. The medical school at a major Cana-
dian university has adopted a patient-centred method as the focus of the
curriculum. This method recognises that the patient has a disease but also
an illness experience that is unique to that individual. The student-centred
programme introduces a case at the beginning of each week. Students
interview the patient, discuss issues and spend the week learning what
they need to know to treat the patient (Western Alumni 1997). Through-
out this process the focus is on the patient, not the therapist.
The above examples might lead to the conclusion that client-centred
practice is fully supported by all health professionals. However, as will be
outlined in this book, there are many aspects of this approach that provide
a considerable challenge to the fundamental beliefs of many therapists.
There continues to be a struggle among health professionals concerning
the conflict that arises between the client’s role in decision-making and
the values of the patient and the professional (Emmanuel & Emmanuel
1992).
All of these issues provided the impetus for this book, which attempts
to facilitate the implementation of client-centred practice. It has been
written for all therapists whether they work as clinicians, managers, educa-
tors or consultants, or are enrolled in an educational programme to
become a clinician. The information is also relevant to therapists in all
work settings, including hospitals, communities, schools, universities and
industries. The focus is both theoretical and practical with an emphasis
on providing solutions to some of the more challenging aspects of
implementation.
Overview of client-centred practice 3
DEFINITIONS
therapist partnership and the need to ensure that services are accessible
and fit the context in which a client lives (p 253).
CLIENT-CENTRED PROGRAMMES
In summary, this model suggests that there are many factors that influ-
ence a person’s performance and which must be considered if the client-
centred approach is to be implemented successfully (Sumsion 1993).
The name of the model was changed in 1997 to the Canadian Model
of Occupational Performance (CMOP) (Fig. 1.3). This version of the
model presents many new concepts. CMOP is a social model which places
the person in a social–environmental context rather than locating the
environment outside the person. The new presentation also recognised
the need to reconfigure the elements so the model appeared less static. It
is now an interactive model showing relationships between persons, envi-
ronment and occupation (L. Townsend, personal communication 1997).
In reality, therapists know that the interaction between the person, their
roles and the environment is quite dynamic and must constantly accom-
modate a variety of changes. The new model allows for change and focuses
on the interaction of the elements.
Self-care, productivity and leisure remain in the middle sphere but are
now considered to be the key components of occupation. The central
sphere now focuses on the person, with spirituality at the core and affec-
tive, cognitive and physical components also featured. The environments
included in the outer sphere are physical, institutional, cultural and social
Overview of client-centred practice 11
tit
Enabling occupation: an
I ns
Pro
occupational therapy Affective
du
are
perspective, p 32. Reproduced
ctiv
lf-c
Social
with permission of CAOT
ity
Se
Publications ACE, Ottawa.)
Physical
Spirituality
Cognitive Physical
Leisure
Performance components Table 1.1 provides the definitions of the four original performance com-
ponents as they appeared in the 1991 version of the Model of Occupa-
tional Performance. The 2002 document of the Canadian Association of
Occupational Therapists has reformulated these performance compo-
nents. The table shows the development of the original four components
– mental, physical, spiritual and sociocultural – which could potentially
be viewed in isolation from each other, into three components – affective,
physical and cognitive – that facilitate interaction. These performance
components have been defined individually in the table but they are all
interdependent.
Occupational therapists are familiar with the affective, physical and
cognitive performance components and regularly consider these in both
assessment and treatment. However, the spiritual component is the most
challenging one for therapists to incorporate into their practice. Its posi-
tion has evolved from being one of the performance components to being
at the core of the Canadian Model of Occupational Performance. This
new position is evidence of its importance. Christiansen (1997) supports
the importance of spirituality by stating that ‘if occupational therapy is to
be complete and genuine in its consideration of humans as occupational
Overview of client-centred practice 13
approach suits the client and providing the necessary education, are also
key components of other approaches. The exception to this harmony may
be the neurodevelopmental approach, which is prescriptive and allows
little client choice, although the decision to use this approach could
be reached in a client-centred way. Therapists should choose the model
of practice that suits the environment in which they work and their
own knowledge and skill, and then combine it with a client-centred
approach.
Another issue that should be addressed before this introductory chapter
is closed is whether or not it is possible to be partially client-centred.
Every qualified therapist knows that the greatest challenge is to find the
right approach, which is as effective as possible for a particular client, and
to apply that approach at the right time and in the right way. It is the
combination of these elements that will enhance a successful outcome. In
this regard client-centred practice is no different from any other approach.
The skill in its successful application is to find the right combination that
the client wants and can accept and that will enhance both short- and
long-term goal attainment. Therefore it would appear that it is possible
to be partially client-centred if the appropriate components are applied to
the individual’s situation based on the client’s goals and the issues pre-
sented by the relevant environments.
CONCLUSION
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– transforming the clinical method, 2nd edn. oriented rehabilitation planning in a single visit: first
Radcliffe Medical Press, Abingdon, Oxon, p 35–52 year review of the quick program. Archives of
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The Code of Ethics – Revised. CAOT Publications Law M 1998 Client-centered occupational therapy.
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Enabling occupation: an occupational therapy practice: what does it mean and does it make a
perspective. CAOT Publications ACE, Ottawa difference? Canadian Journal of Occupational
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Christiansen C 1997 Acknowledging a spiritual Observational study of effect of patient centeredness
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19
Chapter 2
The client-centred approach
T. Sumsion
CHAPTER CONTENTS
Views on the occupational therapy process 20 Client-centred process 24
Traditional approach to intervention 23 Conclusion 27
Reed and In 1983 Reed and Sanderson outlined a problem-solving process model
Sanderson model that followed seven stages:
■ Stage 1 was the referral and initial evaluation, when the therapist gath-
ered information about the client’s occupational performance.
■ Stage 2 – analysis – was then carried out to determine whether or not
this person would benefit from occupational therapy intervention.
■ Stage 3 was a formative evaluation to determine whether the person
was receptive to the concept of occupational therapy.
■ In stage 4, a plan was formulated that considered many aspects of
intervention including goals, media and methods to be used.
■ The programme itself was conducted in stage 5, ensuring that the client
understood what was taking place.
■ Stage 6 was a summative evaluation to determine whether changes
should be made to the programme.
■ Finally, in stage 7, a decision was made to discharge the client and to
arrange any other services that might be required (Reed & Sanderson
1983).
Canadian task This problem-solving process model formed the basis for the work of the
force model Canadian task force that designed the original Model of Occupational
Performance. The client is actively involved in each of the seven stages
of the occupational therapy process that accompanies the conceptual
framework:
■ Stage 1 is the referral stage when it is determined, through a review of
the information received, whether or not the client would benefit from
occupational therapy intervention. The criteria for making this decision
will be determined by the programme within which the occupational
therapist works.
■ Stage 2 is assessment. Data are collected from a variety of sources both
within and outside occupational therapy. Interviews, observations and
specific standardised and non-standardised tools are components of the
assessment which, for an occupational therapist, will focus on task
functioning. A careful review of the accumulated information leads the
therapist to a conclusion and recommendations for intervention, which
are clearly documented.
■ Stage 3 is the programme planning stage when the assessment data are
organized and all elements that would impact on the delivery of the
programme are considered. Planning includes the choice of an appro-
priate model or frame of reference on which to base the intervention
as well as the resources available to carry out that intervention.
The client-centred approach 21
Hagedorn model Hagedorn (2000) reminds therapists that every process is unique and
must be considered within the context of the client’s life. She outlines a
systematic approach to occupational therapy that has five stages, as sum-
marised below.
■ Stage 1: obtaining a profile of the client as a past, present and future
performer of roles and occupations
■ Stage 2: working with the client to specify the problems in achieving
competent occupational performance
■ Stage 3: framing the problem by defining the nature of the situation
within the relevant model
■ Stage 4: identifying what, and in what order, should be done during
the intervention
■ Stage 5: working with the client to explore alternative solutions and
actions and agree on an action plan (Hagedorn 2000, p 77–78).
These processes are fundamental to all interventions planned or carried
out by an occupational therapist. They should be considered throughout
all stages of the client-centred occupational therapy process, which is
described as a linear undertaking but in reality is an ever-changing and
fluid interactive chain of events.
The model of Fearing The view of this process continues to evolve and be influenced by models
and Clark of practice. Fearing and Clark (2000) have outlined an occupational per-
formance process model as a guideline for therapists attempting to be
client-centred in their practice. The reader is referred to Chapter 11 for
22 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Hammell process Therapists are also currently aware of the importance of viewing their
practice from an evidence-based perspective. It is clear throughout this
book that the evidence base for a client-centred approach is growing but
there is still more research needed. Hammell (2001) has recognised the
importance of linking a client-centred approach and evidence-based
practice and provides the following five-stage process to facilitate this
linkage:
■ Stage 1: define the question arising from client-identified issues
■ Stage 2: search the literature for relevant current research papers that
are grounded in the clients’ perspectives
■ Stage 3: critically evaluate the evidence
■ Stage 4: integrate the best research evidence with clinical expertise and
client choice
■ Stage 5: evaluate the effectiveness of subsequent interventions in
relation to the initial client identified needs (Hammell 2001, p 230).
The client-centred approach 23
Other models of Tickle-Degnen (2002) also supports the use of evidence throughout the
client-centred practice client-centred process and suggests that both therapists and clients could
search for research evidence to facilitate the establishment of goals that
are appropriate to the client’s gender, age and diagnosis.
A further framework has been developed by Restall et al (2003). This
framework has five categories that will enhance the use of a client-centred
approach in the therapist’s practice environment. The stages of the frame-
work are:
■ personal reflection which will enhance communication skills and enable
the therapist to learn more about herself and client-centred practice
■ client-centred processes which can be evaluated and facilitated, ena-
bling client-centred behaviours to be modelled
■ practice settings where therapists can advocate for a client-centred
workplace
■ community organising where communities can be informed and
engaged in both development and planning
■ coalition advocacy and political action.
There are some commonalities shared by these various perspectives
that support a client-centred approach, including the client involvement
throughout the entire process with a particular focus on the establishment
of goals and intervention strategies.
CLIENT-CENTRED PROCESS
Referral The stages of a client-centred process may also begin with the receipt of
a referral that the therapist reviews with the client to determine the sug-
gested direction of the intervention. The client’s views on and under-
standing of the reason for the referral are sought in the initial meeting.
The referral does not direct the intervention; rather it provides the reason
for the initial meeting with the client and the impetus for the process to
begin. Negotiation with the referral source may be necessary if the client’s
views of his or her involvement in the process differ from those presented
in the referral.
Assessment and The initial meeting with the client is used to begin to understand the cli-
data gathering ent’s story (Larivaara et al 2001), to gather assessment information in
relation to occupational performance and to explain the parameters of the
programme to which the client has been referred. Communication is a
crucial factor throughout this process and it is made clear from the begin-
ning that the client is an important partner in all stages of the process
(Dressler & MacRae 1998, Pierre 2001, Sumsion 2004). Issues such as
number or length of sessions and programme mandates should be iden-
tified early in the process. The client-centred approach should also be
discussed at this time. This approach warrants some initial discussion, as
it will be new and unique for most clients. The ultimate decision to be
made is whether or not the client wants to participate in the planning
(Söderberg et al 2004) and hence to be engaged in this client-centred
process. The effectiveness of the entire process will be enhanced at this
early stage if the client understands the key issues of this working relation-
ship that will evolve into a partnership.
The focus of the initial meeting is on the client rather than on the
limitations for this particular programme or the system at large. The
therapist discusses the client’s views of the problem for which the referral
was made and their goals and wishes concerning change. It must be rec-
ognised that these goals and wishes may not be in total agreement with
either the reason for referral or the therapist’s choice of the emphasis for
the intervention. Methods of gathering the necessary information, either
about the presenting problems or about possible resources to assist with
the problem, are agreed and a subsequent meeting time is arranged.
Tools are emerging to assist with the client-centred focus of this initial
meeting and assessment:
■ The Canadian Occupational Performance Measure (COPM) is dis-
cussed in Chapter 11 and serves as both an initial interview guide and
an outcome measure. Research has also shown that this tool improves
the client’s participation throughout the process (Wressle et al 2002).
■ The Client Centred Occupational Performance Initial Interview
(CCOPII) was designed for use with clients who have mental health
problems and are living in the community. It is a semi-structured inter-
view based on occupational performance (Orford 1995). Clients are
asked about things that are troubling them and problems that prevent
them from doing what they want to do, with particular emphasis on
self-care, rest or relaxation, work, leisure and relationships. The inter-
26 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Client sets goals In the next stage the therapist and client meet again to discuss all the
information that has been gathered. Time must be spent to ensure that
the client understands the information and has ample opportunity both
to ask questions and to have them answered. A further challenge for the
therapist is to ensure that the client has all of the information that is nec-
essary to make a decision about the goals and methods of intervention.
This may require the presentation of information in a variety of formats
and over a series of sessions. Information may originally be presented
verbally and then in writing, or perhaps by means of a demonstration
either in person or on video. The client needs the opportunity to take
information home for further consideration and to assist with the formula-
tion of questions for future sessions. Types of information will relate to
client strengths and problems, available financial and service resources,
consideration of the environment and other people involved, and the
therapist’s expertise.
At this point the parameters of the programme that were discussed in
the initial session may have to be reviewed. The client needs to understand
the realities and limitations of the available resources before determining
the goals for intervention. The client-centred approach requires that time
and energy be dedicated to the analysis and understanding of the assess-
ment information before the goals are set. The client then sets the goals
(Dressler & MacRae 1998). This is potentially the most important step
in this process. Recent research has shown that clients in an outpatient
mental health programme valued the goals being set in this way and in
reality would not participate in the programme if they had not been
involved in setting the goals (Sumsion 2005). The client owns the goals,
as she or he is the one who will benefit directly when they are met. These
goals also enable all those involved with the client to focus on strengths
rather than problems (Webster 2002). The goals need to be stated clearly
in a format that allows their achievement to be reviewed. Again, time must
be dedicated to the discussion of these goals to ensure that they are clearly
understood by everyone who is involved in or impacted by them.
Partnership to The therapist and client now work in partnership to achieve the goals.
attain goals The therapist has considerable knowledge to contribute to this process
but must also become an educator and facilitator to remove obstacles to
the attainment of the agreed goals. The health professional becomes the
advisor and the client determines the action to be taken based on full
information (Cunningham 2001). Updated information must be pro-
vided and evaluated on an ongoing basis but particularly when there are
new decisions to be made (Hammell 2001).
The client-centred approach 27
Evaluation Forms of evaluation are the same as those for the traditional approach.
Hopefully the one difference will be that the client’s views will be included
in an official way rather than relying on the criteria for success established
by the professionals. In Chapter 9 Marie Gage suggests some methods of
evaluation when working with clients with physical disabilities. The COPM
(presented in more detail in Chapter 11), which was referred to in the
assessment stage, is revisited here and clients rescore their goals according
to their satisfaction and performance.
There are many other methods of evaluation that could be used, includ-
ing a review of the established goals, audits of both the process and specific
interventions, and use of a range of other outcome measures that are
being developed to meet the demands of this stage of the process.
CONCLUSION
All the stages of this process raise many issues that relate to the realities
faced by both the therapist and client, and that will be discussed in sub-
sequent chapters. There are some similarities between a traditional and a
client-centred approach. However, the major difference relates to the role
of the client throughout the process and his or her place as a key player
in all stages. The partnership that is a key ingredient of the client-centred
process cannot occur unless this involvement becomes a major focus of
the intervention. The occupational therapy process should not be treated
superficially. Rather, there should always be clear evidence that this is a
carefully considered process with clear documentation of the contribu-
tions and responsibilities of all members of the partnership at each stage
of the process.
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29
Chapter 3
Environmental considerations
T. Sumsion
CHAPTER CONTENTS
Specific environments 30 Physical environment 35
Cultural environment 32 Social environment 35
Institutional environment 33 Conclusion 36
SPECIFIC ENVIRONMENTS
CASE STUDY: MR C
Mr and Mrs C are both 83 years old and have been married for 56 years.
They have no children and live in a two-storey, 100-year-old house on her
family’s farm. The bathroom is on the upper level. Most of the land is rented
but there is still a large yard and garden for them to maintain. Mrs C has
run an antique business for many years and continues to do so on a part-
time basis. Mr C is an accountant. Both Mr and Mrs C are licensed drivers.
Mr C began to experience extreme low back pain. After extensive tests
and the involvement of several doctors he underwent surgery to fuse two
discs in his lower back and emergency surgery 2 days later to relieve
spinal pressure. Mr C was in intensive care for 2 weeks, spent some time
on a surgical ward and was subsequently transferred to a spinal cord
rehabilitation facility. Their home is 100 miles from the rehabilitation
centre so Mrs C could visit only when someone was able to drive her
or she was able to take the train on her own. On admission to the
rehabilitation facility Mr C was unable to walk, turn himself over in bed,
eat or dress independently, and could not write or use the telephone. He
worked extremely hard at his rehabilitation and 3 months later could
walk with a walker, feed himself, dress his upper body and use the
telephone.
Four months after his admission to the rehabilitation centre Mr C
was able to return home for a 5-day visit. The staff at the centre made
arrangements with the local home care office for an occupational
therapist to visit the home to discuss environmental barriers, a nurse to
visit daily and a homemaker to come twice for 3 hours while Mr C was
32 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
CULTURAL ENVIRONMENT
have been for many years. But there are issues that must be addressed.
Everyone is part of a variety of cultures and subcultures (Sumsion 1997).
In this case the rural subculture must be considered as people in this
culture simply get on with dealing with the challenges presented by life.
The elements are a constant challenge with which rural people deal. In
order to survive, they have to be independent but at the same time they
are also willing to help a neighbour. In this culture you only have to ask
for help once and it is provided. The men on neighbouring farms readily
provided assistance with problems of wheelchair access and troublesome
catheters. Others drove several miles to the pharmacy to collect prescrip-
tions and checked to see whether other provisions were required.
The sick role is also an important consideration when discussing the
cultural environment. Clearly this couple was not prepared to adopt this
role. Independence and function are important to them and they were
determined to maintain this state. The importance of family within any
culture must also be considered. However, this couple does not have any
children or any family close enough or well enough to be of assistance.
A major cultural issue relates to the occupational therapist and her lack
of understanding of the importance of culture to this couple. She did not
acknowledge that they live in a heritage home, which they were not pre-
pared to alter. Nor did she acknowledge the strength of character of an
elderly rural couple who are very assertive. They have good ideas and
know what is best for them. They do not respond well to being told what
to do. Overall, this therapist did not use a client-centred approach (see
also the related discussion in Ch. 6).
INSTITUTIONAL ENVIRONMENT
PHYSICAL ENVIRONMENT
SOCIAL ENVIRONMENT
2002). This environment also involves providing a place where clients can
feel safe, both physically and emotionally, and valued which enables them
to explore their potential (Rebeiro 2001). Social aspects of the environ-
ment such as lively neighbourhoods, attitudes of others and family support
also influence the client’s engagement in meaningful activities (O’Brien
et al 2002). Lilja et al (2003) further concluded that social support was
an important component in enabling older people to perform activities
of daily living. Social expectations are both formal (such as laws) and
informal (such as traditions), and greatly impact on our ability to partici-
pate in daily occupations (Christiansen & Townsend 2004).
Mr and Mrs C do not have a large family but they do have many friends
who are part of their chosen family. Many volunteers, such as the driver
from the Red Cross who drove Mrs C to the city to visit her husband,
also became friends and formed an important part of this environment.
Their farm is on the edge of a small village where many people have lived
all their lives. This longevity forms close social ties that are strengthened
in times when assistance is needed. Their antique business has a national
reputation, which also enlarges their social circle and assists the village by
giving it a position of prominence.
Social roles must also be considered. Hospitals are a social environment
where those who are ill are expected to conform. In that hospital environ-
ment Mr C was not expected to make a full recovery. However, at home
he was viewed as a vital man who had a role as a husband and farm
manager. In this environment there was faith in his strength and abilities
and he responded to this in very positive ways. A positive social environ-
ment accepts the person for what they are and encourages them to be
whatever they wish. Mr C progressed to enjoy his garden, which he
planned and organised, although a friend did the heavy work. He drove
his car and enjoyed a rich life where all his roles were supported and
encouraged.
CONCLUSION
This case discussion has emphasised the need for therapists to become
familiar with assessments that will enable them to evaluate the influence
of all environments. All of the four environments must be considered in
light of the individual circumstances presented by each client. Some envi-
ronments will emerge as being of greater significance than others, but all
must be considered. These environments have been discussed in isolation
to stress their importance but in reality there is considerable overlap
between them. For example, the friends from the rural environment who
were so willing to be of assistance form part of both the cultural and social
environments. Therapists also work within a changing environment that
presents an increasing number of challenges that will influence their ability
to support the client’s goals in each environment. However, this does
not lessen their responsibility to consider all environments and to work
with the client to establish a list of priority issues that will influence goal
attainment.
Environmental considerations 37
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39
Chapter 4
Implementation issues
T. Sumsion
CHAPTER CONTENTS
Definition of client 39 Client-centred language 45
Power 41 Barriers to client-centred practice 46
Therapist as educator 44 Conclusion 51
Client choice 45
This chapter discusses the issues that add challenge to the implemen-
tation of client-centred practice. These issues include the importance
of clarifying who is the client, the shift of power from the therapist
to the client, the therapist as an educator, client choice and safety,
and client-centred language. The barriers to client-centred practice
presented by the therapist, the client and the working environment
are also discussed.
There are many issues a therapist must address before effectively imple-
menting a client-centred approach. Many therapists believe that client-
centred practice is inherent in occupational therapy, which has a tradition
of using a holistic approach. Therefore, it may appear that no alterations
are required as, by its very nature, occupational therapy is client-centred.
It is true that if all aspects of the Canadian Model of Occupational Per-
formance were addressed with every client, then a truly holistic approach
has been used. However, there are many issues related to both the appli-
cation of the individual components of the model and the overall philoso-
phy of client-centred practice that must be considered if one is to be an
effective client-centred therapist.
DEFINITION OF CLIENT
POWER
■ have to advocate for clients who are labelled as difficult because they
will not comply with treatment that is not directed toward their goals
■ need to be supporters of the self-help movement which meets the needs
of clients that therapists are unable to address
■ have to express views that differ from those of the other members of
the multidisciplinary team.
Clients will set goals that seem unreasonable but they need to be helped
to work toward those goals. An 80-year-old man needs help to drive again
rather than the creation of obstructions simply because this goal appears
unreasonable. A disabled mother needs creative solutions that will allow
her to bottle-feed her child rather than being told to accept that others
will do this for her. A troubled adolescent needs help to find alternative
educational organisations rather than being told he must conform to the
traditional system. These may be radical examples, but the challenge of
client-centred practice is to facilitate by the transfer of power rather than
to obstruct by maintaining that same power.
The overriding skill that will make all this happen is communication –
true, in-depth, open and honest communication. Only this will allow the
therapist to understand what clients really want and need, and enable
them to understand the realities of the system that may either facilitate
or impede attainment of the desired goal.
THERAPIST AS EDUCATOR
It has previously been established that clients cannot make the necessary
decisions unless they have all the relevant information. Ideally, clients
should always be given sufficient information to enable them to make
informed decisions (College of Occupational Therapists 2000). The chal-
lenge for the therapist is to present this information in a way that is clearly
understood by the client. This necessitates skilful communication abilities
to assess which method of education will be most successful with various
clients. Some will respond more effectively to written information while
others will need the information described or demonstrated. Some will
want to take the information home to discuss with others before making
a decision. Clients are also becoming generally more informed as a result
of access to the internet and will therefore be entering the process as more
informed consumers (Richards 1998). In this situation therapists must be
prepared to work with information that is presented to them and which
may challenge their knowledge base or beliefs and values. Bridson et al
(2003) summarise this issue by stressing that therapists should change
their approach from disclosing to sharing information.
When educating clients about the challenges they face it is important
to elicit their ideas, check their baseline information and understanding,
and elicit questions from them. Education is also important during the
negotiation, which determines the focus of the intervention. Again it is
important to check understanding and to elicit the patient’s preferences
and commitments. Motivation will be enhanced if solutions are negoti-
ated. Timing is also a crucial factor in the transmission of information.
Implementation issues 45
Clients are under considerable stress and may not be able to absorb the
knowledge required before making a decision (Deber 1994). Therapists
must be sensitive to this stress and ensure that the provision of informa-
tion acknowledges and accommodates the realities of the information
being discussed. Communication is a crucial factor in education. If thera-
pists listen and respond at the appropriate level then learning is enhanced
for both the therapist and the client.
CLIENT CHOICE
CLIENT-CENTRED LANGUAGE
approach to intervention, would use when meeting with a client for the
first time. It is likely that conversation would include a statement such as:
‘You are here because the consultant asked me to see you.’ In client-
centred practice this wording would not be used; rather, the client would
be asked why she was there so that her role as decision-maker might be
established immediately.
In a subsequent meeting to discuss the results of the assessment the
therapist might traditionally have said: ‘Based on the results of the assess-
ment here are the goals that we will be working toward.’ In the client-
centred approach the results would be discussed with the client rather
than presented to him. Following receipt of all the necessary information,
provided in a way the client can understand, the client then determines
the goals for the intervention.
Words must support actions, as was previously mentioned in the section
on power. The actions necessary to be truly client-centred will not occur
if the process does not begin with, and continue to include, the words
that convey a commitment to this approach and to the client’s central
role throughout the process.
Therapist barriers Therapists have a responsibility to ensure that the goals set for interven-
tion are safe and that no harm will come to the client. This is relatively
Client safety easy to achieve in the traditional approach to intervention as the therapist
uses professional judgement to determine what is safe. However, the
potential exists in a client-centred approach for the client to determine
goals that the therapist thinks are unsafe or that entail unnecessary risk
(Law et al 1995). Work by Sumsion and Smyth (2000) revealed that
therapists present other barriers by having goals that differ from those of
the client, allowing their values and beliefs to prevent them from accepting
the client’s goals and being uncomfortable letting the client choose their
own goals. A repetition of this work in Sweden found that the highest
ranked barrier was the therapist not having enough knowledge about
client-centred practice. The findings in this study also supported the first
two barriers in the study by Sumsion and Smyth (2000) (Wressle &
Samuelsson 2004). There is no easy answer to this dilemma. If clients
have the right to make decisions about their plans, and if the therapist
has provided all of the necessary information to ensure that clients under-
stand the risks of their decision, then clients have the right to make a
seemingly unsafe choice (Clemens et al 1994).
Implementation issues 47
Therapist confidence Therapist confidence may also present as a barrier and is an important
issue to consider before deciding to implement a client-centred approach.
It has already been mentioned that it takes confidence to support a client’s
decision in the face of opposition from other team or family members. It
also takes confidence to be certain that all the necessary information has
been provided to the client in a way that was thoroughly understood
before reaching a decision. Therapists must have confidence that their
knowledge base is sound enough to support the information being
requested by and given to the client. Barriers will certainly arise if the
therapist lacks either knowledge about client-centred practice or self-
knowledge (Fraser 1995, Law et al 1995). Self-knowledge ensures that
the therapist is comfortable with personal boundaries and the reality of
limited capabilities. Clients may want to establish goals that are quite
unrealistic. It takes confidence to reassess the information given to the
client that led to the establishment of that goal and to reframe the infor-
mation for further review.
48 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Other therapist There are many things that are part of a therapist’s being and hence mould
components how he or she approaches the partnership with a client. These include the
therapist’s values and beliefs, which must have an impact on how the tasks
are performed. If the therapist believes that humans are innately strong,
then expecting clients to cope with a wide range of adversities will guide
the interventions that are suggested. On the other hand, if the belief
system focuses on human weakness, then the expectations will have a dif-
ferent focus. Beliefs and values are complex but therapists must clearly
understand their own foundation and how this impacts on their approach
to clients. The therapist’s personal values must also be separated from the
professional ones, as well as from the client’s values. This can be a particu-
lar challenge if the client is making a decision that the therapist views as
unsafe (Law et al 1995).
The therapist’s skills at building rapport will also have a major impact
on the ability to adopt a client-centred approach. In order for clients to
accept power they must trust the person who is assisting them with that
responsibility. This development of trust begins at the first encounter and
continues until the process comes to an end. If a positive rapport has been
established, the client will not fear asking questions, which is an essential
ingredient in ensuring that information is understood and fully informed
decisions are made. It is less difficult to ask what may appear to be an
embarrassing or insignificant question if you have a meaningful relation-
ship with the person who has the answers.
Other barriers that the therapist might bring to the encounter include
ethical considerations, ability to access information and general commu-
nication skills. Is it ethical to refuse funding that would help an elderly
client who is reluctant to have bath rails installed because they will ruin
the decor she has planned so carefully? The therapist knows that with
these rails the client would be able to bathe independently and safely.
Without them she will be in serious danger of falling and will require
expensive home help. Volumes have been written about ethics and ethical
dilemmas, and the issues will not be resolved here. The point being made
in this discussion is simply that the way a therapist views the ethics of the
situation may prevent the application of a client-centred approach. The
client has the right to refuse the bath rails but the therapist must have
confidence that this decision was made following receipt and understand-
ing of the relevant information that addressed all available options.
The importance of the client having the information needed before
making a decision has already been addressed. However, a barrier is
created if the therapist is unable to access the necessary information. This
Implementation issues 49
Client barriers The barriers that may be presented by the client fall into several catego-
ries. The first relates to social and family issues. Krupat et al (2001)
found that younger white women and those with a higher income had
a greater desire to share, which is an essential element of client-centred
practice. Older people have trouble making decisions due to limited
information and organisational structures that impact on the coordina-
tion of services (Parkinson 2004). Clients may traditionally have lacked
power and are therefore in a position where they fear what will happen
to them if they do not comply with someone else’s wishes. They may
be intimidated by hospital staff or professional people in general, and in
the therapeutic environment will choose not to take responsibility for
themselves. Clients in one study clearly stated that some staff interactions
made them feel uncomfortable, vulnerable and frightened (Sumsion
2005).
Education may also be a barrier. Clients may lack an understanding of
the rationale behind client-centred practice or the confidence that comes
with advanced levels of education. They may lack previous opportunities
to question information that is given to them and hence be reluctant to
admit that they have not understood the presented material.
Cultural issues, discussed in Chapter 3 in relation to the cultural envi-
ronment, may also pose barriers to the client taking full advantage of the
client-centred intervention. Their culture may encourage the maintenance
of the sick role and the acceptance of how sick people perform. This per-
formance may not include accepting the power to make decisions about
the goals and means to accomplish them. Clients may also be expected
to maintain a stiff upper lip and not to complain or disagree with the
direction the intervention is taking. They may see the professionals as the
experts and expect them to take a leading role and direct the intervention.
The client may also simply be too ill or tired to expend the energy required
in making decisions.
Problem-solving skills are required to participate fully in client-centred
practice. When clients do not possess these skills, therapists may have to
be more directive than would be their choice when attempting to imple-
ment this approach (Law et al 1995). Additional client barriers presented
by an older client group are discussed in Chapter 7.
Issues related to the Client-centred practice works in harmony with other models and
multidisciplinary team approaches. However, it is difficult for an occupational therapist to use a
client-centred approach if the other members of the team follow a tradi-
tional approach and are more directive. Harrison (2001) cautions that
medical teams may do what they think is best but without listening to
what the client wants. Confusion will result for clients who are being
advised by the occupational therapist that they can determine the goals
for the intervention, while being told by other team members what course
of action to follow. Frustration will result for the therapist who wants to
champion the client’s chosen course of action but who knows that the
decision will not be supported by other members of the team. This issue
is very closely connected to the earlier discussion related to therapist
confidence. It takes considerable courage to tackle a team in order to
support a client’s choice in the face of opposition which inevitably carries
more power if only because of the number of people who are opposed.
The reality in the healthcare system now relates to budget pressures,
staff shortages and accelerated client turnover (Coulter & Dunn 2002,
Lane 2000). The financial priorities of the programme may not allow the
flexibility of taking more time to help a client establish goals that are
personally meaningful. Eligibility criteria are tightening, along with
resources and services that can be removed with little warning (Parkinson
2004). There may not be the resources for the establishment of pro-
grammes that would truly meet the client’s needs. If the programme is
dominated by the medical model, it may be difficult to implement client-
centred practice. The key components of client-centred practice, such as
autonomy and responsibility, do not fit with a system that insists on being
staff led. Funding is usually directed toward the issues that are outlined
in the philosophy of the programme and hence there are problems in
securing funding for programmes that counter the favoured approach.
CONCLUSION
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55
Chapter 5
Implementing client-centred practice
D. M. Parker
CHAPTER CONTENTS
Introduction 55 Strategies for implementing client-centred
Issues in implementing client-centred practice 65
practice 57 Conclusion 71
INTRODUCTION
Clinical Area 1
Venue: A busy acute physical department, part of a major Foundation
Teaching Trust providing regional and supraregional specialties with a
high level of clinical expertise and tertiary referral service.
Occupational therapy team: Nine qualified staff
Beds: 500 inpatient beds.
Clinical field: Neurosciences, oncology, cardiology and transplantation
programmes in cardiac, liver and renal specialties.
Unique features: The occupational therapy team members were a cohesive
group. Each worked independently as part of a multidisciplinary team
on their own ward areas. Liaison was important both internally with
other therapists, ward staff and social work teams, and externally with
community-based staff providing community care, transfer and discharge
provision. Throughput was heavy with much emphasis on fast and
efficient discharges.
Model of care: Medical model in the hospital.
Clinical Area 2
Venue: A hospice based in the community providing palliative care.
Occupational therapy team: Two senior therapists and a junior
therapist.
Beds: 25 inpatient beds; outpatient and day care.
Clinical field: All conditions of adult oncology and palliative care with
some referrals from neurosciences.
Unique features: The occupational therapy staff were an integral part of
the multidisciplinary team within the hospice. Patient and carer
involvement was closely linked to therapeutic care.
Model of care: Client-centred.
Both of these areas have presented with their own difficulties and chal-
lenges in implementing client-centred practice and should supply the
reader with some insight into the issues and solutions. They will be
referred to throughout the chapter.
Service issues Ideally there should be some process by which a clinician or manager
agrees which model of practice is to be adopted by themselves or their
Internal pressures team. This process may be an internal one; for example, perhaps you as
a manager are not aware of which model of practice your staff is using.
Taking on new staff, new graduates or students often raises interest in
approaches to practice as they challenge existing styles and models. The
impetus for change may come about by sharing new ideas and innovations,
or by challenging existing practice and knowledge. In addition, closer
working relationships with other occupational therapy services within a
local health economy may indicate a clear and obvious need to affirm and
link models of practice to support the focus of the patient pathway.
External pressures Alternatively, the impetus for change may be external. For example, gov-
ernment policy usually dictates the direction of change within local health
services which in turn affects the way in which occupational therapists
deliver intervention. Recently the drive in the NHS has been towards
encouraging patient choice and patient involvement in health care, with
the emergence of Patient Councils and the Expert Patient. In addition,
the modernisation agenda in the UK emphasises partnership with service
users and a genuine involvement at every level of service delivery (Depart-
ment of Health 1997, 1998, 1999, 2000, 2001). This development cer-
tainly works in favour of the client-centred model of occupational therapy
as it reinforces much of the philosophy described within the definition
refined by Sumsion (2000a). This definition is described in Chapter 1.
Other developments at strategic level may also influence and initiate
change in practice. For example the publication of National Service
Frameworks (Department of Health 2004) in the UK send very clear
messages about how health care is delivered by a skilled workforce able
to meet the needs of clients.
Managers and therapists should be clear about terminology. They
should not confuse client-centred practice with patient-focused care, and
should not allow health service bosses to be confused about the differ-
ences between these approaches. It is the manager’s responsibility to
ensure that, if adopting the client-centred approach, it is identifiable in
practice.
Patient-focused care is clearly defined as ‘the re-design of patient care
so that hospital resources and personal care are organised around patients
rather than around various specialised departments’ (British Association
of Occupational Therapists 1994, p 1). It is distinctly different from
client-centred practice. Patient-focused care may be interpreted as
Clashes with other A third reason for considering the client-centred approach is evolutionary.
approaches Here the clinician or manager may identify a natural shift in practice away
from the mechanistic reductionist medical model of practice to a more
humanistic or social model linked more clearly to the roots of occupa-
tional therapy. Sumsion (1993) supports the concept that client-centred
practice is a greater challenge than traditional models and that it provides
a good example of where we can use our clinical reasoning skills. Client-
centred practice creates a natural balance between the medical and social
models of care as it can be applied in either of these environments.
Falardeau and Durand (2002) compare some of the dimensions of the
medical model of practice with a client-centred approach and illustrate
the differences between the two.
The definition of client-centred occupational therapy has been rede-
fined and reshaped, involving therapists throughout the United Kingdom
(Sumsion 2000a). This work recognises the social reality of resource
constraints and the requirement for joint goal planning, as well as placing
partnership, listening and respect firmly within the occupational therapy
domain.
Once the decision has been made to adopt a client-centred approach,
attention to the following issues will facilitate that process, as adopting a
model of practice is as much about practical changes as philosophical
affirmation.
Staffing issues The decision to adopt a client-centred approach must be endorsed by the
occupational therapy team if it is to be implemented with success. They
Compliance need to embrace and understand how the model of occupational perform-
ance – which forms the basis for client-centred practice – works (Sumsion
1997). This model was updated in 1997 to the Canadian Model of Occu-
pational Performance (CMOP) (see Fig. 1.3), and using this will support
practice across the service. Compliance is a conviction that should be
tested in practice. In other words, therapists who say they are client-
centred, but whose language, manner and the way they deliver therapy is
carried out to the exclusion of the client, clearly require challenging in
their understanding of this approach.
Role model In any team, the effect and influence of role models should never be
underestimated. Key senior staff can exert considerable influence over
juniors and students, and provide both positive and negative role models
(Kielhofner 1992). Strong leadership can take new ideas forward and
provide a creative environment for ideas to develop, to be challenged and
tried out. Positive role models may emerge through practice observation,
shadowing and teaching specific techniques, as well as by influencing
practice through sound supervision, personal mentoring, professional
support and focused objective setting. The influence of experience over
and work with others within the group, thus providing a focus for team
building. Oakland (1989) places teamwork, involvement and problem-
solving firmly within the context of successful quality management. In
addition, purposeful and positive groups help people to make positive
changes, especially if the relationships within the group provide the
members with a sense of trust and safety (Goleman 2002).
Team support can also assist in exploring difficult issues in client-
centred practice such as cases of conflict. Consider this example:
In Clinical Area 1 a therapist is carrying out a client-centred pro-
gramme and setting up the discharge for an elderly man for whom
there will be risks at home. Conflict arises when the relatives insist the
man should be placed in a nursing home to be cared for. The client is
fully aware of the risks and is adamant about going home. The therapist
has carried out a client-centred assessment and has identified the prob-
lems with the client and actioned solutions. Whilst the therapist feels
sure she is acting in the client’s best interests and expressed wishes, she
is worried about the reaction of the relatives. She talks this over in
supervision and agrees to present this case at the next team training
session. The team members discuss the case and actively support the
therapist in her analysis of her intervention, challenging her to recog-
nise where she is delivering client-centred care, encouraging her to act
as the client’s advocate and to prepare her argument in support of the
client against the views of the relatives.
This is an example of the challenge a therapist may face when facilitat-
ing the shift in power to the client. The will to transfer this power illus-
trates the shift from the medical paradigm to that focused on a client’s
needs (Falardeau & Durand 2002). Harnessing team support will ensure
greater success in implementing client-centred practice.
Management support There is no doubt that implementing any change in practice requires not
only time and commitment from staff but also support and encourage-
ment from occupational therapy and service management. In order for a
service to be truly client-centred, there needs to be commitment from all
levels in the organisation. Wilkins et al (2001), in a study looking at
qualitative results from three different study populations, considered
aspects of difficulty when implementing client-centred practice. Chal-
lenges were identified at service, therapist and client levels. At manage-
ment level this means a commitment to the principles of client-centred
practice, with open communication, support and education being the key
issues. This may take the form of approved study time or time out from
clinical work for discussion and reflection, or the provision of training
resources, for example purchase of the Self Instructional Package for the
Canadian Occupational Performance Measure.*
Provision of research opportunities – time, library facilities, research
guidance, literature searching, etc. – to explore the theory and practice
* The COPM Self Instructional Package is available from the Canadian Association of
Occupational Therapists and the College of Occupational Therapists in England.
Practice-related issues Once the commitment has been made to adopt a client-centred approach,
the next stage for planning is to determine how to put the approach into
Conflict practice. Managers should be aware of the environment in which their
teams function and the philosophical approach used, however indistinct
this may be. Adopting client-centred practice may cause conflict for occu-
pational therapists with others in the wider multiprofessional team who
adopt a very different approach. A note of caution should be heeded that
professional rivalry and conflict over roles may seriously disadvantage the
client, who may be caught in the middle (Wright & Rowe 2005). Teams
that focus on the needs of the client and work together will better meet
the client’s goals.
The most common conflict in the work environment is likely to be a
clash with other models (see Ch. 1), particularly the medical model with
its rather mechanistic, diagnosis-led approach which can ignore the indi-
vidual in the bed. Conflict is most obvious in the acute sectors of the
health service where pressure on beds and the urgency to discharge chal-
lenge the role and purpose of occupational therapy (Blain & Townsend
1993). In practice, many therapists consider that the main conflict between
client-centred practice and the medical model remains an issue of control
and timeliness of intervention rather than an overwhelming philosophical
issue (Parker 1995).
In clinical practice, the most common barrier to implementing the
client-centred approach is where the client and the therapist have dif-
ferent goals (Sumsion & Smyth 2000). Some of this discomfort may stem
from the values held by the therapist preventing them from ac-cepting
the client’s goals or from a reluctance to allow the client to choose their
own goals. These difficulties can be resolved by establishing an educa-
tional programme which focuses on how to practise in a client-centred
manner, negotiated goal setting, case studies providing clear client-centred
examples, and structured interview training to support therapists to use
effective listening and communication skills and goal planning.
The conventional approach may be for the therapist to inform the client
that she will be writing to inform his doctor, who will then contact the
vehicle licensing authority.
The client-centred approach would be to share with the client what
the cognitive deficits were and explain their effect on function. In addi-
tion, the consequences and possible outcomes of his actions need to be
explored to enable the client to understand the risks involved in his course
of action in order for him to understand and take responsibility for his
own actions.
An additional impact of using a new technique is having the time to
use it properly, especially when the demand to vacate beds, organise dis-
charges or manage waiting lists is a constant pressure. This may affect the
quality and standard of the service. Managers need to provide support
to therapists struggling with a philosophy and approach that may place
them in conflict with colleagues over intervention, discharge and case
management.
Therapists who fail to grasp the holistic nature of the client-centred
approach may struggle with forming realistic intervention plans which
truly reflect the client’s expressed needs. Consider the case study from
Clinical Area 1. In this example a therapist identifies risks of safety but
the client has not identified any – and indeed denies there is a
problem.
Education and training First of all, know your staff. This may sound obvious, but knowing their
strengths, weaknesses, interests and skills will help to establish a clear
profile of your workforce. It will help you, the manager, to identify resource
issues, training needs, extra support and eliminate problem areas.
It has been noted already that introducing client-centred practice is
best supported by education and training (Parker 1995, Sumsion 2000b,
Ward et al 1996), which should address issues of low confidence and poor
skills. Similarly, there is evidence in the literature to support that training
providers of health care, such as occupational therapists, in a client-
centred approach can impact positively on patient outcomes (Lewin et al
2004), which reinforces the need to ensure that staff gain confidence in
client-centred practice through training and education.
For example, in studies on the introduction of the COPM, results
showed that low confidence levels in administering this measure were a
significant factor in the poor uptake of the measure, as well as training
being a vital part of its application (Parker 1995, Ward et al 1996). By
contrast, those who felt more confident and who used the COPM more
fluently demonstrated a greater practical awareness of client-centred prac-
tice. Confidence can be gained if practice and service delivery are endorsed
as client-centred from the top. Teamworking can provide peer support,
and supervision can be used to clarify performance and applaud achieve-
ments. Confidence in being client-centred will remain low if the safety
net of peer support and supervision is removed and good practice is not
applauded.
The following practical suggestions may be of help:
■ Team-working: Cohesion and support from the occupational therapy
team will provide peer trust and good communication, both of which
are vital for implementing new approaches. Team building is imperative
if a new philosophy which will affect practice is to be introduced. This
can be achieved by training ‘away days’ on aspects of client-centred
practice with an agreed action plan, timed implementation programme
and named key personnel. Team building should also incorporate
regular review sessions to monitor progress, determine difficult issues,
and formulate and agree a way forward.
From theory You might also want to consider the following ideas to consolidate your
into practice strategy for implementing client-centred practice:
■ The client-centred practice philosophy should be reflected in depart-
mental standards which structure the quality of practice. There should
be a clear statement, endorsed by staff practice, which reflects the
client-centred approach throughout the whole of the occupational
therapy process.
■ Encourage client feedback about your service with questions directed
at eliciting an evaluation of the approach used by your staff. This might
be achieved by phone or postal questionnaire, or by targeting specific
client groups within the service and carrying out evaluative interviews
(Hebert et al 2000) or focus groups.
■ Display the model of choice on noticeboards and in clinical files. For
example, the Canadian Model of Occupational Performance (CMOP),
on which client-centred practice is based, has an excellent diagram
which clearly represents the model (Canadian Association of Occupa-
tional Therapists 1997) (see Fig. 1.3).
■ Develop client-centred practice as a working philosophy expressed in all
areas of contact with the client. For example, check that the department,
the service and any marketing literature are client-centred and friendly.
■ Review all paperwork and forms to reflect a client-centred approach
and ensure that forms are completed with the client. If resources
permit, then self-duplicating assessment forms or intervention sum-
maries would allow clients greater ownership, control and compliance
by having access to information on their treatment.
■ Establish evidence-based practice resource files for literature on client-
centred practice and related subjects. Staff in Clinical Area 2 have
worked hard to collate evidence-based material to support a client-
centred approach in palliative care that particularly reflects the values
of the hospice movement.
■ Case note audit and team audit of standards can similarly monitor
practice and detect changes in approach towards client-centred prac-
tice. In Clinical Area 1 the team decided, as a result of their peer audit
of case records, that they wanted a positive statement on client agree-
ment to intervention included in the audit checklist.
■ Develop interviewing skills by use of case studies and video feedback
of practice interviews (Wressle et al 2002). Encourage the critique
and evaluation of staff members’ interviews to establish a standard in
interviewing. Again in Clinical Area 1, staff requested feedback on
interviewing skills as their confidence needed boosting in carrying out
client-centred interviews.
■ Use the Self Instructional Programme for the COPM which includes
a video and notebook. This encourages close observation and critical
analysis of various client-centred interviews, which can act as a fine
teaching and learning tool.
■ Purchase other learning tools which incorporate practical tuition, for
example Enabling Occupation: A Learner-Centred Workbook (Townsend
& Wright 1998).
■ Establish the evaluation of outcomes within the department. Use of
the COPM will ensure that the client-centred approach is used. Analysis
of its administration may also highlight difficulties with client-centred
practice.
■ Provide feedback to the staff team on the change in practice, either by
encouraging self-evaluation of performance or by the analysis of out-
comes data, complaints or compliments about the service. Feedback
can also be given individually through supervision and appraisal.
Planning intervention ■ Use a client-centred assessment tool and check that this considers an
individual’s concerns about occupational performance issues (Sumsion
2000b).
■ Listen to how the client explains their concerns (Sumsion 2005).
■ Use a client-centred model of practice to frame intervention (e.g. the
CMOP).
■ Consider using the COPM to capture a client’s occupational perform-
ance issues and engage them in evaluating their own performance
(Pollock 1993).
■ Provide the client with options and choice about interventions (Rebeiro
2000b).
■ Explain the process of occupational therapy intervention.
■ Name, frame and agree goals together (Fearing et al 1997).
■ Explore and support clients in the challenges and risks required to
promote change (Townsend 1999).
Finally, the question must be considered: Why use this approach? Please
do not just take my word for it: you must go out there and consider all
the options for yourself. You know your own unique staff team, the
demands and constraints on your service, and the resources available to
you. You must make that decision.
There is no doubt that being client-centred is challenging. It demands
a high level of commitment, time and training. Staff need to be good
‘people therapists’ who can interview effectively and efficiently, commu-
nicate succinctly and clearly and work with clients to identify jointly
agreed goals. For clients who struggle with the responsibility of making
choices about their future, the therapist needs to exercise sensitivity and
clarity in order to empower them. With other clients who have problems
of insight or intellect, the therapist needs to maintain their involvement
while not losing sight of the goal or discounting their limited
interaction.
Client-centred practice, however, does have definite advantages, not
least because by following this approach we are adhering to the standards
set by the professional bodies of occupational therapy, the College of
Occupational Therapists in the UK and the Canadian Association of
Occupational Therapists, to name but two. There is evidence in the litera-
ture that development of a client–therapist partnership can lead to
increased client participation, client self-efficacy and improved satisfaction
with the service. It is an approach that promotes respect for the partner-
ship between therapists and clients (Law et al 1995, Sumsion 2000a).
CONCLUSION
This chapter has explored the issues which may face a clinician, team
leader or manager who is considering implementing a client-centred
approach into their service, reflecting issues from both a staff and a prac-
tice point of view. The manager needs to empower and encourage the
development of the team in order to achieve this goal. Practical strategies
are suggested but they are not an exhaustive list. If managers are to dem-
onstrate their own leadership skills then they must base their strategy for
client-centred practice on their unique knowledge and understanding of
their team and the constraints and opportunities facing their service.
Managers must have their own vision.
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Chapter 6
Using a client-centred approach with
persons with cognitive impairment
S. J. G. Hobson
CHAPTER CONTENTS
Clients with cognitive impairment 75 Strategies for client-centred care with persons
Capacity to participate in client-centred with cognitive impairment 79
care 77 Case example 84
Conclusion 86
Ontario’s Consent to Treatment Act (Bill 109 1992) explains that the
person must ‘understand and appreciate’ the information necessary to
make a reasoned decision. This includes understanding the information
listed above, that the condition affects him/her, and the impact of the
treatment on his/her life and quality of life.
It is clear that the cognitive demands implicit in client-centred care are
significant. In fact, it is considered an advanced form of clinical reasoning,
called conditional reasoning, for the therapist to project a realistic antici-
pated future for a given client (Fleming 1991). It is therefore understand-
able that questions are often raised about the ability of a client with
cognitive impairment to participate in this sophisticated form of decision-
making. However, these concerns seem to come from the professionals.
Client advocacy groups serving those with cognitive impairments are clear
in stating that such clients deserve to participate in treatment decisions.
The Brain Injury Association of America states that rehabilitation pro-
grammes should promote self-determination and that consumers and
their families know their needs best. Further, clients with brain injury have
identified that being included in the treatment planning process helped
them to feel in control of their treatment, and indicated that ‘their feelings
of “relationship” with the providers were the most important part of
therapy’ (Darragh et al 2001, p 194). Similarly, the Alzheimer Society
(2005b) supports diagnostic honesty, because ‘people with Alzheimer
Disease need to participate in decision-making regarding their daily lives
and future care for as long as they are able’ (Guiding principles, paragraph
4). The Alzheimer Society’s ethical guidelines further reinforce the right
of persons with dementia to participate in care decisions by stating that
‘a diagnosis of Alzheimer Disease, in itself, does not mean that a person
is immediately incapable of making decisions. However, as the disease
progresses, a person’s decision-making abilities will change’ (Alzheimer
Society 2005a, paragraph 2).
Karlawish (2004) provided objective evidence to support this, noting
that the decision-making abilities of individuals with mild to moderate
dementia were qualitatively different from those of individuals with mod-
erate to severe dementia, as demonstrated by Mini-Mental State Examina-
tion (MMSE) scores. He went on to note that measures of decision-making
ability were not associated with severity of psychiatric symptoms either.
However, Latvala et al (2004) suggest that ‘patient oriented mental health
care varies depending on the patient’s needs and situation, from depend-
ence to independence’ (p 615).
Competence is both a medically and a legally defined construct. In the
literature, the term capacity is sometimes used in lieu of competence. For
clarity, in this chapter the term capacity will be used to refer to the medical
Using a client-centred approach with persons with cognitive impairment 79
Despite the many difficulties identified above, there are four specific strate-
gies that may assist the therapist in implementing client-centred care with
persons with cognitive impairment. These strategies include enhanced
client assessment, graded decision-making, advocacy and surrogate client-
centredness. These strategies will be discussed in turn.
Enhanced client Occupational therapy practice has been described as including seven steps:
assessment referral, assessment, programme planning, intervention, discharge, follow-
up and programme evaluation (CAOT 1991). During the assessment
phase, the client with cognitive impairment may have difficulty providing
80 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Extended history-taking During the assessment process, as noted earlier, the client with cognitive
impairment may have difficulty providing a comprehensive and coherent
history. If this is the case, additional efforts will have to be made to obtain
detailed background information about a client. As indicated, this back-
Using a client-centred approach with persons with cognitive impairment 81
ground is important so that the therapist can offer the client a suitable
range of options from which to make choices. If the client has had a life-
long interest in gardening, for instance, a horticulture programme may
be a more suitable therapeutic activity than playing adapted checkers. This
is particularly important when allied with graded decision-making, to be
discussed next.
Extensive knowledge about the client can also assist the therapist to
more accurately interpret the client’s wishes, especially when the expres-
sion of these is equivocal or difficult to understand. An example of this,
with which many therapists are familiar, is the failure to report pain in an
effort to be a ‘good patient’ who is seen as compliant and/or cooperative.
Those close to the client may be able to advise the therapist of other
indicators of discomfort, such as becoming unusually withdrawn or quiet.
Particularly difficult for therapists to fully understand may be highly idio-
syncratic use of certain colloquial expressions. For example, the word
‘tolerable’ is a term of high praise for a friend of mine. Someone who did
not know her well would very likely misinterpret her use of this word,
assuming she intended the customary meaning of ‘barely acceptable’,
when she would use it to convey great satisfaction.
Law et al (1995) state that respect for diversity, formerly called cultur-
ally sensitive care (Anderson et al 1990) or culturally competent care
(Spector 2000) and now more usually called culturally safe care (Notter
et al 2004), is an important part of client-centred care. This is critical,
because clients from non-western cultures may have very different beliefs
about the causes of health and illness (Adler 2004). Further, clients with
cognitive impairment may be unable to explain cultural values and needs,
but they may still respond negatively to any breech of cultural ethics,
however inadvertent. Simple things, like shaking hands (Mouton & Villa
2004, Tran & Yeo 2004), making direct eye contact (Mouton & Villa
2004, Tran & Yeo 2004) and standing too close (Adler 2004) may be
intrusive or even insulting to clients of some cultures. It is also important
to recognise that even knowing the cultural mores of a particular group
may not be sufficient, because individual members may be more or less
acculturated to western ways (Adler 2004), and not all members of any
given culture subscribe to all of its values (Spector 2000). The therapist
can learn from significant others which particular cultural values the client
may have held dear and, thus, avoid giving unintentional offence.
Family members and close friends can offer this type of background
information about a client, and they are usually pleased to be asked to do
so. They are gratified to see such interest in the client as an individual. It
is important to note that it may be necessary to gather information from
several sources. This is particularly true when there is no consistent and/
or long-standing companion or caregiver, such as a spouse, available.
Advocacy Occupational therapists often work in teams where not all professionals
subscribe to client-centred principles, and they are accustomed to advocat-
ing to the team on behalf of their clients. Advocacy is especially relevant
when competence is called into question, because conformity is known to
play a large role in competence decisions (Venesy 1994). ‘The question of
competence is rarely raised unless there is an issue of non-compliance’
[with medical advice] (Fulbrook 1994, p 458). Further, the very fact of
having a cognitive impairment may put a client at risk of being treated as
Using a client-centred approach with persons with cognitive impairment 83
CASE EXAMPLE
The following case is drawn from the author’s clinical experience. It was
this case that first sparked an interest in the topic of client-centred practice
with clients with cognitive impairment. It is also where the strategies of
graded decision-making and advocacy were first tested. The case example
may serve to illustrate use of these strategies.
upholstery. He indicated that this ‘red sports car’ would help him ‘catch
all the sexy girls’. The chair for which Nick expressed this preference was
too wide. Other chairs fit better, but he always stated that he wanted the
‘red sports car’. When asked to consider elements of the chair other than
colour, such as comfort, he would only reiterate that he wanted the ‘red
sports car’.
Realising that this approach to wheelchair selection was too complex
for Nick, several attempts were made to simplify the task; in other words,
to implement graded decision-making. First, sequenced steps were used.
The fit and comfort of the chair would be decided before addressing
colour. Questions were phrased so as to eliminate the effect of colour,
while addressing the priority characteristics. For example, Nick would be
asked whether he would like this chair better than the red one if this one
were also red. Under this circumstance, he responded in terms of the
comfort of the chair or how easily he could ‘drive’ it. However, Nick still
became overwhelmed by the array of choices, and he could not remember
which chair was most comfortable.
The next modification to the decision-making process was to impose
a framework. The number of options with which Nick had to deal at
any one time was limited. Nick was assessed on only two chairs per
appointment. Within this limited array, he was able to express clear and
consistent messages about comfort and ease of propulsion, though the
issue of colour arose at every session over the next several weeks.
Once the issues of fit, comfort and ease of propulsion were finalised,
it was time to deal with the issue of colour. Nick had expressed a
strong, sustained and consistent desire to have a red wheelchair. Before
beginning to assess the various wheelchairs, funding and the fact that
Nick would have to pay for the chair had been discussed. He was aware
of the fact that he did not have control of his finances and indicated that
they were controlled by ‘the government’. When he was informed that
there would be an additional cost to have a red chair and that this
surcharge would not be subsidised by the government programme but
would have to be paid entirely from his funds, Nick said: ‘Is worth it.’ He
went on to say that he had ‘never had sexy red sports car before’ and
that it would help him ‘catch all the girls’ now that he was no longer
young. He was reminded that the extra expenditure would have to be
authorised by his trustee. In response he said: ‘Is my money. I can pay.’ It
was time to implement advocacy.
A letter was sent to Nick’s trustee clearly explaining the need for a
wheelchair, the various necessary features, the total cost, the proportion
subsidised, and the outstanding expense against Nick’s estate. No
difficulty was anticipated in obtaining approval for this. The difficulty
might arise over the extra cost of the colour option. The letter went on to
explain the additional cost and the fact that this would not be subsidised.
It also stated openly that this was not an entirely necessary expenditure.
However, the letter went on to explain how sustained and consistent
Nick’s preference was, pointing out that he had even preferred a red chair
over one he admitted was more comfortable. Nick’s reason for wanting
86 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
the red chair was not detailed, but the potential impact of colour on his
acceptance of the wheelchair was mentioned. The letter also detailed
Nick’s awareness of who managed his finances, the extra cost of the
colour option, and his belief it would be worth it and that he could
afford it. The letter closed by urging the trustee to authorise the extra
expense if Nick’s finances allowed it.
Some colleagues scoffed at the idea of advocating for a red chair for
Nick. One stated that he probably would not even remember wanting a
red one by the time his chair was delivered, and others derided the waste
of time and effort, because the trustee would never approve such an
unnecessary expenditure. As the occupational therapist in the case, this
author never felt that this was a waste of time. Occupational therapists
strive to be client-centred, and these actions were directed to that end.
Nick had participated in the decision-making process and had expressed
a clear preference for a red chair. There was reason to believe that he was
capable of making that decision, as demonstrated by the consistency of
this desire over a period of several weeks, his willingness to pay extra for
this feature, and the fact that he had a clear rationale for his decision. The
fact that he called the wheelchair a car or that others might not agree
with his rationale was peripheral to the issue of capacity. He had passed
the ‘understand and appreciate test’.
In the end, the trustee consented and Nick got his red chair. That
decision provided some degree of vindication in the eyes of colleagues,
but the use of a client-centred approach, adapted by graded decision-
making and advocacy, was appropriate whatever the outcome. There is
support for this stand in an informal poll of approximately 60 occupational
therapists working with clients with cognitive impairment. They enthusi-
astically agreed that occupational therapists should listen to and respect
client opinions and preferences, even when the client has cognitive impair-
ments and/or has been found legally incompetent (Hobson 1996).
CONCLUSION
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91
Chapter 7
Using a client-centred approach with
older adults
S. J. G. Hobson
CHAPTER CONTENTS
An ageing population 91 What should the therapist do differently? 100
Pioneers in ageing 92 Conclusion 103
How are older adults different? 95
AN AGEING POPULATION
The world is experiencing what has been termed an ‘age wave’ (Dychtwald
& Flower 1990). This is a global phenomenon, with the number of indi-
viduals age 60 and older projected to rise 223% between 1970 and 2025
(World Health Organization [WHO] 2002). Even this ageing population
is ageing, particularly in developed countries, where people over age 80
are the fastest growing segment of the population (WHO 2002). In fact,
one American source reports that centenarians are actually the fastest
growing sector of the population, with those aged 85–99 the second
fastest growing (Boston University Medical Campus). Explanations for
this phenomenon include decreasing fertility rates, as well as increasing
longevity (WHO 2002). This latter has been attributed, in part, to medical
advances that have extended life expectancy (Dychtwald 1999). A third
factor, which is accelerating the effect of the other two, particularly in
Europe, Australia and New Zealand, and North America, is the ageing of
92 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
the post World War II ‘baby boom’ (Dychtwald 1999). The eldest
members of this cohort turn 65 in the year 2011. The World Health
Organization has stated, ‘measures to help older people remain healthy
and active are a necessity, not a luxury’ (WHO 2002, p 6).
Given this demographic imperative, it should be clear why a separate
chapter has been allocated for the discussion of client-centred care with
older adults. Most occupational therapists will have some exposure to the
care of those over age 65 and, for many therapists, this group will form
the majority of clients seen.
This chapter will consider older adults as a group, looking at their
typical life circumstances and how these may influence treatment planning
as well as exploring how the elderly are different from younger adult
clients, particularly in terms of their health status and the attitudes that
may influence the clients themselves and their caregivers, both profes-
sional and informal. Specific recommendation about what therapists
should do differently for these clients will follow. None the less, therapists
are reminded that the hallmark of client-centred care is individualisation
of care, and this information may not be pertinent to all older adults –
apply it only as appropriate to each of your individual clients.
PIONEERS IN AGEING
Given that, until recently, few have lived to what we now consider old
age, today’s elderly have been described as pioneers (Kiernat 1991).
Occupational therapists seeking to offer client-centred care to older
adults need a context within which to plan treatment (Law et al 1995).
Individual older clients may be more or less typical of their cohort, but
it is useful to understand the cohort realities in order to frame the right
questions or to recognise how unique a given client’s experience may be.
In addition, given that ‘old age’ is generally considered to start at age 65
and many now live into their nineties, it is important to remember that
old age may include several cohorts. Today’s ‘young old’ adults (65–74
years) are quite different from the ‘old old’ (85+ years), which is only to
be expected given the differences in their age and life experiences.
This section will outline some of the unique life circumstances of the
cohort now pioneering old age that occupational therapists routinely
consider when planning treatment, such as living arrangements and the
availability of financial resources (Table 7.1). Women live longer than
men, so the older client is more apt to be a woman, and she is apt to be
a widow. Should the client be a man, he is probably still married, and thus
may be expected to have more social support available (Age Concern
England 2004a, Statistics Canada 1999). The older client will probably
live in his/her own home, but as age advances so does the probability of
moving into rental accommodation or of placement in an institution (Age
Concern England 2004a, Statistics Canada 1999). Overall, Canadian rates
of institutionalisation are higher than those in England (Age Concern
England 2004a, Statistics Canada 1999). Factors such as population
mobility, climate and geography have been suggested as contributing to
this (Forbes et al 1987).
Using a client-centred approach with older adults 93
Table 7.1 Life circumstances of the population aged over 65 years in the UK and Canada
Attribute United Kingdom Canada
Gender distribution Women: 57.5% of those age 65+ years Women: 57.4% of those age 65+ years
Men: 42.5% Men: 42.6%
Housing 65–74 years living alone:* 65–74 years living alone:
18% of men 13.8% of men
34% of women 29.8% of women
75+ years living alone: 75–84 years living alone:
29% of men 18.6% of men
60% of women 49.2% of women
85+ years living alone:
28.6% of men
57.8% of women
Institutionalisation 65–69 years: 4% 65–74 years: 1.9%
(e.g. sheltered 70–74 years: 7%
accommodation) 75–79 years: 10% 75–84 years: 8.9%
80–84 years: 13%
85+ years: 19% 85+ years: 33.8%
Poverty 17% of men Almost half of seniors living alone
21% of women Over half of women living alone
Income sources 69% of pensioner households depended 40% of income from government pensions:
on state benefits for at least 50% of 46% for men 65+ years living alone
income 62% for women 65+ years living alone
bilities, older people are particularly vulnerable’ (WHO 2002, p 30). The
financial ability to participate in leisure occupations that enhance quality
of life may be particularly threatened, because it is well known that low
income older adults expend the majority of income on basics like food
and shelter (Statistics Canada 1999).
Canada and the United Kingdom also both have socialised medicine,
whereby basic medical care is provided free to all citizens. However, in
some jurisdictions, some health-related expenses (e.g. medications, assis-
tive devices, etc.) are not fully covered. Britain has broader healthcare
coverage than Canada (Novak 1993), particularly in terms of their devel-
opment of community healthcare initiatives, which were not funded under
Canada’s early medicare system (NACA 1995). The United Kingdom has
‘official guidelines [that] call for 1.5 full time equivalent home help aides
per thousand population . . . compared to an estimate in the early 1980s
of 0.5 per thousand in Canada’ (Forbes et al 1987, p 49). This sector of
health care has grown rapidly in Canada. Public home care expenditures
doubled between 1991 and 1997 (NACA 1999a), and the number of
home support workers and agencies for seniors ‘increased by at least 50%
in the last decade’ (NACA 1993, p 12). Use of formal home care supports
is linked to increasing disability and to lower levels of informal assistance
(Stone & DeWit 1991). It is important to note, however, that it is not a
case of using either formal or informal supports. Often both are needed.
Informal caregivers may access formal supports when the strain of caring
undermines their own health or to supplement their efforts at informal
care (NACA 1995). Further, many older adults use commercial services
to supplement both formal and informal supports (Hobson 2004).
Beyond considering the formal supports available to the elderly, it is
equally or more important to consider informal supports, because an
estimated 80% of all long-term care is provided by family members and
friends, outside of hospitals, nursing homes or other institutional settings
(Dychtwald 1999, NACA 1999a). Such informal support is three times
as likely to come from women as men (Dychtwald 1999). Because women
tend to live longer, many older men may receive care from their wives,
but the typical caregiver is a 45- to 55-year-old woman who works full
time outside the home (Dychtwald 1999). Male and female carers tend
to approach informal care differently, performing different types of tasks
and offering different types of support (Corcoran 1992, Turk-Charles et
al 1996). Women usually provide direct personal care and offer emotional
support, whereas men typically assist with financial matters and home
maintenance and offer instrumental support, such as managing care
(Corcoran 1992, Turk-Charles et al 1996). Where the spouse is the
primary carer, it is important to recognise that the caregiver may be just
as elderly as the client. Of an estimated 6.8 million carers in the United
Kingdom, 3 million are seniors (Age Concern England 2004b). Where
the caregiver is an adult child, it is important to remember that many face
dual caregiving responsibilities – for children as well as parents – which
has led to the term the ‘sandwich generation’ (Dychtwald 1999). In fact,
adults can now expect to spend more years caring for parents than children
(Dychtwald 1999).
Using a client-centred approach with older adults 95
There are two main categories of differences between younger and older
adult clients that will be addressed specifically in this chapter. These
include the overall health status of the client and the attitudes held both
by the client and by society at large. Both will influence efforts to deliver
client-centred care.
Sensory change Function in all senses declines as we age (Bottomley & Lewis 2003), but
not all senses decline at the same rate (Levy 1986). Although taste, touch,
smell and vestibular senses are all affected and important, they will not
be the focus here, because changes in these senses have less direct impact
on client-centred care than changes in vision and hearing.
Hearing loss associated with the ageing process, known as presbyacusis
(Taber’s 2005), is the third most common disease of the elderly (Taber’s
2005). It is estimated to affect one in three of those over age 60, and up
to half of those age 85 and older experience hearing loss (National Insti-
tute on Deafness and Other Communication Disorders [NIDCD] 2005a).
This form of loss is not necessarily a complete inability to hear; it is more
often associated with difficulty in discriminating high frequency sounds,
including consonants, which affects people’s ability to understand speech
(NIDCD 2005b). As such, it can lead to enormous frustration and anxiety
in social situations, and it will certainly affect occupational therapy assess-
ment and treatment.
96 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
There are many causes of visual deterioration in later life. These include
presbyopia, poor accommodation for close vision associated with the
ageing process (Taber’s 2005), cataracts, glaucoma and diabetic retinopa-
thy (Desai et al 2001). The leading cause of visual deterioration in those
over age 50, however, is macular degeneration, where the centre of the
individual’s field of vision deteriorates and vision in this field becomes
blurred (Bothwell 2004). Overall, 92% of those over age 70 need glasses,
but a further 14% of community-dwelling adults aged 70–74, and 32% of
those over age 85, have visual problems not corrected by wearing glasses
(Desai et al 2001). Again, such deficits will naturally impact on occupa-
tional therapy assessment and intervention for affected clients.
Co-morbidity A co-morbid disease is one that coexists with but is unrelated to the
primary reason for seeking health care (Stedman’s 2005). Older adults are
more likely to display co-morbidity than younger clients, primarily because
of their likelihood of having chronic health problems. Among Canadians
over age 65, 6% report no health conditions, 31% report one or two, 30.7%
report three or four, 18.3% report five or six, and 13.9% report seven or
more coexisting health conditions (Canadian Study of Health and Aging
Working Group 2001). These chronic health conditions, in descending
order of frequency, include arthritis, hypertension, cardiac problems,
respiratory problems, visual difficulty, emotional problems and diabetes
(Canadian Study of Health and Aging Working Group 2001).
Recognising the presence of co-morbid conditions is essential to occu-
pational therapy, because these conditions may complicate and/or prolong
recovery from the presenting diagnosis. For example, a client admitted
for a hip fracture may have his/her recovery complicated by the presence
of arthritis in the knees and hands, which could impede use of assistive
devices, such as a walking frame.
A concomitant of having multiple health problems is an increased prob-
ability of taking multiple prescriptions and over-the-counter medications
(Fulton & Allen 2005). In addition, many older adults use complemen-
tary and alternative therapies, such as herbal remedies, that interact
with prescribed and over-the-counter medications (NACA 2005). This
polypharmacy may complicate an older client’s recovery because of the
increased risk of toxic interactions among medications. All healthcare
professionals involved with the older client must be alert to this possibility,
but the occupational therapist, who often is the team member to visit the
client’s home, may be in the best position to discover the extent of
polypharmacy.
Frailty Because many older adults already have one or more chronic health pro-
blems (Age Concern England 2004a, Canadian Study of Health and
Aging Working Group 2001, Statistics Canada 1999), they are vulnerable
to other health problems. These include secondary medical complications
(Bottomley & Lewis 2003), adverse medication reactions (Fulton &
Allen 2005) and malnourishment (Bottomley & Lewis 2003). Further,
the ill effects of these problems are greater in older clients. Brummel-
Smith (1990) suggests that once one thing extra goes wrong, the older
Using a client-centred approach with older adults 97
Attitudes Attitudes have a pervasive and subtle influence on all behaviours, so atti-
tudes toward the ageing process and about the elderly will naturally affect
healthcare delivery when working with older adults. We learn attitudes
from significant others and from life experiences (Shilton 1995), so natu-
rally attitudes vary among cultures (Bonder 2001). The role of the media
and humour in attitude development are also recognised (Webb & Tossell
1999). This section will briefly consider some of the attitudinal influences
unique to working with older adults, including ageism, health beliefs,
patterns of under-reporting health problems and the potential influence
of the life experiences of older clients.
be sure that these are not influencing treatment decisions (Bottomley &
Lewis 2003, Squire 2002), to challenge overt instances of therapeutic
nihilism (Brummel-Smith 1990) and to work toward setting goals that
are realistic (Bonder 2001, Bottomley & Lewis 2003) for every client,
regardless of age.
Health beliefs Individuals have widely varying conceptions about what health is (Adler
2004, Spector 2000) as well as about what causes illness, what treatments
are most likely to be effective and whether to consult health professionals
(NACA 2005). Health and illness beliefs are strongly influenced by culture
(Adler 2004, Spector 2000) as well as sociodemographic factors such as
gender, age, education, income and social connections (Galanos et al
1994, Strain 1989).
Older adults may perceive the medical professions more positively and
rate their medical care more highly than younger adults (Beisdecker 1996,
Thorson & Powell 1991). Older adults demonstrate lower health self-
efficacy than younger ones, which influences actions taken to enhance or
manage health, including treatment decision-making (Beisdecker 1996).
Reduced health self-efficacy could have a major impact on client-centred
practice, given that its founding principle was that the client retained
responsibility (Rogers 1951).
Many older clients may assume a passive role in healthcare interactions.
They ask fewer questions, disagree less often and seem more content to
have professionals make treatment decisions (Beisdecker 1996, Putnam
1996). This may be, in part, because they revere the professional (Thorson
& Powell 1991) or because they are intimidated by his or her knowledge
(Hofland 1992). Extreme regard for health professionals may lead the
older client to fear taking too much of the professional’s time or to
unrealistically expect the professional to know what is wrong without
needing to be told (Hofland 1992). These attitudes are undesirable in
terms of establishing the partnership mandated by client-centred care,
because the passive role they inspire contradicts the premise of client
involvement in treatment planning. On the other hand, the leading edge
of the baby boom generation reach age 60 in 2006. The youngest of
today’s older adults are more highly educated (Colyer 2004), are much
more computer literate (Age Concern England 2004a, Ryan 2001) and
are using the computer to access health information (Colyer 2004, Ryan
2001). These factors make them much more active consumers within the
healthcare system, which may make client-centred practice easier for the
therapist.
Under-reporting Both ageism and health beliefs are closely tied to the issue of older
adults under-reporting health concerns. Particularly prone to be under-
reported are pain (NACA 2002), incontinence (Health Canada 1999),
falls (Tideiksaar 2001) and elder abuse (NACA 2003–2004). One of the
commonest reasons for failing to report health problems is fear of loss of
control when the healthcare system gets involved (Hofland 1992), most
particularly fear of being placed (Rogers & Holm 1994, Tideiksaar 2001).
This is a valid concern, in that incontinence frequently strains relationships
100 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Life experience It has been said that we are the product of our upbringing and experiences
(Lohman & Spergel 2004). Older clients bring a lifetime of experiences
to the therapeutic relationship. They have a long history of facing life’s
challenges, which may have enhanced their coping strategies (Turk-Charles
et al 1996). They have a lifetime of habits that may be difficult to change,
although Kiernat (1991) argues that such habits are efficient. Many of
the oldest older adults bring vastly different life experiences than most of
their much younger healthcare providers, specifically personal experience
of the Great Depression and of World War II (Lohman & Spergel 2004),
and among some immigrant older adults, of prejudice (NACA 2005) or
even victimisation. Some clients may also bring attitudes no longer widely
accepted, including racial intolerance and strongly differentiated sex roles.
Client-centred practice requires a respect for diversity, even when therapist
and client values diverge (Law et al 1995).
Client-centred care has been the topic throughout this entire book, but
there are some adjustments to this approach that may be necessary when
working with older adults because of the unique characteristics of this
client population that have been discussed in this chapter. Four key rec-
ommendations for modifying the client-centred approach when working
with the elderly follow. These include adjusting the degree of client
control, modifying communication strategies, cultivating trust and
rapport, and challenging ageism.
Adjusting the degree The most global change that may be necessary with an older adult is
of client control allowing him or her to establish the degree of client control. Because of
their respect for medical professionals (Thorson & Powell 1991), some
older adults may prefer to rely on the professional’s advice (Beisdecker
1996, Putnam 1996) and feel very uncomfortable with the idea of telling
the professional how therapy ought to unfold. Older adults are more
externally oriented in terms of health locus of control (Beisdecker 1996,
Gebhardt et al 2001), and this may be reflected in a more passive response
to therapy decision-making.
Using a client-centred approach with older adults 101
Clients may also assume a passive role in the healthcare system because
of past experiences as a patient (Beisdecker 1996). The traditional medical
model of care invests the physician with authority over the patient (Barris
et al 1988). With this as the basis of their experience, clients may be sur-
prised or alarmed when asked to assume a decision-making role in their
care, because they expect the professional to know what is wrong (Hill
1995) and what to do about it.
The client’s desire to participate in treatment decisions may also be
influenced by type and severity of illness (Ford et al 2003). Further, their
desire for information regarding their diagnosis or care may vary from
individual to individual (Epstein et al 2004) or at different points in time
during the therapeutic relationship within the same individual (Anthony
& Hudson-Barr 2004). It is also important to note that individuals’ desire
for information may be greater than their desire for involvement in
treatment decisions (Ford et al 2003, Putnam 1996).
One strategy for encouraging clients to exercise more control that this
author has used is to provide the information needed for informed deci-
sion-making, explain why the information is germane, and offer advice
only after that. This makes the therapeutic rationale clear and offers the
client the opportunity to voice an opinion should he or she wish to do
so. Occasionally clients have done so at decision points later in therapy,
perhaps having gained confidence in their ability to understand and master
therapeutic decision-making. Lang et al (2002) recommend asking ques-
tions specifically designed to elicit the clients’ perspective on the cause of
the problem during the initial interview, in order to involve them more
fully in the care process, which increased their satisfaction with their care.
Another strategy that works well for some decisions (e.g. selection of
therapeutic activities) is to offer a range of choices that all provide similar
benefits and explain that they all will meet the goals equally well. Epstein
et al (2004) call this ‘declaring equipoise’. None the less, some older
adults may wish to be less involved in making treatment decisions (Anthony
& Hudson-Barr 2004, Epstein et al 2004), and this should be respected
(Putnam 1996).
Challenging ageism As has been discussed, the healthcare environment is not immune to
ageism. It may be demonstrated overtly, when clients are labelled ‘bed
blockers’ to imply that they somehow have less right to occupy a hospital
Using a client-centred approach with older adults 103
bed than younger patients or, more subtly, when older clients get less
direct treatment time (Beisdecker 1996, Bottomley & Lewis 2003, Shilton
1995). One of the key concepts of client-centred practice is ensuring that
the client has access to services (Law et al 1995), and this may require
the therapist to examine personal attitudes as well as to challenge ageism
in colleagues or within the healthcare system to ensure that older clients
get equitable access to care.
CONCLUSION
Entire books are written about the treatment of the elderly; this chapter
is only trying to focus on using a client-centred approach with older
adults. This approach requires that therapists ‘determine who the client
is [and] respect the client’s value system and culture’ (Law et al 1995,
p 254). To that end, this chapter has considered the typical life circum-
stances of older adults, some unique factors influencing their health status
and attitudes that affect the care of the older adult. Specific suggestions
on how to modify a client-centred approach in response to some of
these unique characteristics include adjusting the degree of client control,
modifying communication strategies, cultivating trust and rapport, and
challenging ageism.
It is essential to note that this chapter can only consider what is usual
for older adults. The essence of the client-centred approach is to recognise
the individuality of the client. Armed with some information about this
increasingly diverse population (NACA 2005), it is now up to readers to
determine to what extent, if any, this is applicable to each older client they
treat.
References
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107
Chapter 8
Ask, listen and learn: what clients
with a mental illness can teach you
about client-centred practice
D. J. Corring, J. V. Cook
CHAPTER CONTENTS
One therapist’s experience of listening to clients relinquishing outdated assumptions and
and changing her approach to practice 107 practices 111
Psychiatric rehabilitation and recovery: principles Lessons learned: studies of the client perspective
and practices 108 on issues in mental health 113
The values and strategies of qualitative Implementing client-centred practice in mental
research 110 health: a ‘to do’ list 116
Implementing a client-centred model: Conclusion 120
When describing what she learned from a qualitative research study with
clients with severe and persistent mental illness, Susan Nagle (1997) wrote:
As an occupational therapist I prided myself on the fact that I stressed
clients’ strengths and did not focus on their illness. The findings of this
study have made me step back and recognize that I should give a client’s
illness more thought. Though I always want to emphasize what clients
can do I must remember that the illness experience is a devastating one
108 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Cook (2001) examined the way in which the values, beliefs and language
of occupational therapy are consistent with those of qualitative research
inquiries. She stated:
I want to understand the world from your point of view. I want to know
what you know in the way you know it. I want to understand the
meaning of your experience, to walk in your shoes, to feel things as you
feel them, to explain things as you explain them. Will you become my
teacher and help me understand?
Ask, listen and learn 111
everybody ‘should do’ and focus on what they ‘want to do’. Occupational
therapists have to stop using the DSM-IV as a primary reference point
and use instead the lived experience of the client as the primary reference
point. Occupational therapists have to give up the notion that these clients
‘can’t do’ and focus on what they can do. Performing a functional assess-
ment that looks at what a client can’t do, sends a message to your client
that you are focusing on their deficits before getting to know them as an
individual, and may result in them lowering their expectations about
themselves and their abilities. Professionals who do not seek to understand
the person behind the illness, who treat the individual as an illness rather
than as a human being, and who fail to respect the individuality of the
person’s needs, add to the burden of those living with the illness (Corring
2004b).
Professionals, including occupational therapists, must stop thinking
about what is different about the world of the person with a severe and
persistent mental illness and focus instead on understanding what things
in their world mean to the individual. We need to stop the practice of
asking retrospective questions to inform our treatment and rehabilitation
plans, and replace them with our observations of the ‘ordinary round of
everyday activities’ in their life (Angrosino 1998, p 268). Angrosino
relates his work with a client named Vonnie Lee, a person labelled as
mentally retarded. He talks of what he was able to learn and understand
about Vonnie’s world once he allowed himself to think differently:
My encounter with Vonnie Lee taught me that his worldview was not
a failed approximation of how a ‘normal’ person would cope, nor was
it, when taken on its own terms, intrinsically disordered. His fixation
on the bus is only ‘disordered’ or an ‘attempt at adjustment’ if we
assume the rest of us are not without our own fixed ideas regarding the
world and our place in it. Were we to suffer the misfortune of being
labeled ‘retarded’, would all of our ideas, attitudes, and practices stand
up to scrutiny as being unimpeachably ‘normal’? Once we start looking
for evidence of ‘disorder’, then ‘disorder’ is almost certainly what we
find. If anything, Vonnie Lee’s logic is more clearly worked out and
better integrated than that of more sophisticated people; his ‘retarda-
tion’ may, indeed, lie in the way he has purified his obsession down to
its basics rather than veiling it in varieties of symbolic discourse like
‘normal’ people do. Interviewing him in a way that arose out of normal
activity did not merely ‘contextualize’ his disorder, it removed the
emphasis on disorder altogether (p 267).
Client perception of Corring and Cook (1999) describe the elements of client-centredness
client-centred care from a client perspective. The results focus on two themes: the client in
the client–service provider relationship and the client in the social and
mental health service systems. Clients describe what’s wrong, what’s
needed and how they have been affected. Clients defined client-centred
care as requiring the service provider to adopt a caring, positive and
welcoming attitude, to develop full relationships with their clients, to find
common ground with their clients in order to build partnerships, to
ensure that clients are involved in informed decision-making, to facilitate
recovery, to not tolerate stereotyping and stigmatising behaviours, to
ensure accountability and to advocate for laws that protect vulnerable
individuals (Corring 1996, 2004a). Perhaps occupational therapists should
assess the client-centredness of their practice using these parameters.
Client satisfaction Client satisfaction with services has been emerging as an important
outcome domain within the mental health field. The direct involvement
of consumers of mental health programmes in the development of outcome
114 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
The client in the Another qualitative study used a narrative approach to explore a client’s
community life story of living with a severe and persistent mental illness. Three main
themes were identified: the early years, being in hospital and being in the
community. The first theme was organised into two categories that
recounted experiences of early family life in a family living in poverty. The
second theme revealed the client’s experience with early symptoms of
illness leading to hospitalisation, the experience of being in hospital
and the learning that occurred in hospital. The final theme described pre-
vious attempts at community living that were unsuccessful, the current
successful experience of community living, the realisation that there was
more to learn, and future hopes and dreams. Reading this client’s story
enables the reader to gain an understanding of the life experience of one
client living with severe and persistent mental illness (Labbe & Corring
2003).
Over the last 30 years, people with severe and persistent mental illness
have moved from traditional institutional settings into the community.
Little attempt has been made, however, to understand the client’s experi-
ence of living in community-based residential settings and their percep-
tions of what makes for a satisfactory quality of life. A qualitative single
case study explored one client’s life experiences within two community-
Ask, listen and learn 115
based settings. The overall theme that emerged was the importance of
having a dream. Embedded in this theme was the importance of various
environmental characteristics and their impact on the client’s quality of
life. Important environmental characteristics included personal freedom
and choice, physical environment, social environment, opportunities to
learn new skills, presence of structure without restriction and opportuni-
ties to live a ‘normal life’ (Mallon 1999). Studies by Rebeiro and Cook
(1999) and Rebeiro (2001b) also describe the importance of social and
cultural environmental factors in providing clients with satisfying experi-
ences. Therapists can learn from these studies that the occupational con-
texts are every bit as important as the occupational doing and merit their
attention.
Work and productivity A study that examined the lived experience of work for individuals living
with mental illnesses found that there were many challenges that work
presents for them. Themes included the challenges in their pursuit of
employment, the benefits they felt as part of a supported work programme
and finally the importance of work in terms of self-esteem, self-confidence,
adding structure to the day, overall life satisfaction, socialisation and a
feeling of contributing to society (Willis 2000). Corring (2004b) reports
116 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Self-care Another qualitative study (Rowan 1999) that asked individuals with
mental illness how they would define self-care indicated that self-care
involved several broad components, including health practices, coping
mechanisms, responsibility and routines, enjoyment, pleasure and soli-
tude. Factors that impacted on a person’s function in the area of self-care
were the person’s state of health and the person’s subjective feeling about
self. Interventions guided towards the individual’s feeling about his/
herself may prove more effective at promoting self-care than interventions
targeted directly at the individual’s health and hygiene practices. In addi-
tion, increased interventions in the areas of coping mechanisms and
symptom management may improve the individual’s ability to function in
all areas, including self-care.
Quality of life All of the individual lessons that can be derived from these studies are
reiterated and comprehensively explored in two studies that examined
quality of life issues for individuals living with severe and persistent mental
illness (Corring 2002, 2004b). These studies reported that quality of life
was dependent on achieving management of the illness, establishing sup-
portive relationships, maintaining meaningful occupation and developing
a positive sense of self. Occupational therapists who understand the
importance of such experiences can do much to positively impact on
quality of life for these individuals in a client-centred way.
and skills needed for effective rehabilitation. The three phases of psy-
chiatric rehabilitation involve multiple steps in diagnosing a person’s
readiness for rehabilitation and the required skills and the needs for
resource acquisition or modification. The planning phase requires
details of the who, what, when, where and for how long of intervening
to provide services. The intervention phase puts into action those plans
in terms of skill development and use, and resource development and
use. An effective process of rehabilitation requires all three phases
within an agency designed in terms of the psychiatric rehabilitation
values which are consistent with the values of client-centred occupa-
tional therapy. In order to accomplish effective rehabilitation, both
therapists and their employer must be committed to the time, patience
and commitment required to meet the programme objectives.
■ Thus, occupational therapists have to become the cultural leader/
change maker. Occupational therapists need to implement a culture of
client-centred/client-directed practice/rehabilitation by living the
principles, and ensuring the use of appropriate language and practices
that fit the culture. In a study of innovation and leadership in mental
health, Cook (1995) describes the pivotal role played by an occupa-
tional therapist who used her professional values as a resource and
mandate for action. By constantly, over a period of 3 years, maintaining
a cultural vision and language of client-centred practice she accom-
plished her goal of instituting individual rehabilitation and support for
persons with schizophrenia. The clinic she brought into being was the
first of its kind in Canada. This therapist was not in an administrative
position when she began her quest, but was able to persuade others to
join it. No matter what our position in the agency, community or
hospital, we can and must be cultural change agents.
■ Since empowerment is a participatory, learning process that changes
power relations, everyday practice is an important arena for producing
change. Changes in daily routines, interactions and structures are prac-
tical ways of engaging in empowerment, even if these produce only
localised shifts in power. For professions who claim to be client-centred,
such as occupational therapy, the call is to actually be client-centred in
the talk, actions and structure of everyday practice – to demonstrate
and facilitate participation, social change, collaboration, reflection,
experience, risk taking and inclusiveness in the everyday arena
(Townsend 1998).
■ As occupational therapists we must teach, advocate and enable envi-
ronmental exposure and education. We have to start with ensuring the
person has a base knowledge of their illness and then understand what
they can do and what they want to do. Susan Duff (2005), 2004 CAOT
Innovative Practice Winner commented:
I think it is important to ask yourself who are you working for; what
do people say they need; what is the best thing you can do. Advocacy
is a big issue – probably more so in mental health but perhaps it’s the
same in other areas. There are a lot of issues with long term progres-
118 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
sive illnesses, from the quality of life that people enjoy, drugs that are
covered, or not covered, programming for employment and things
like that. You can’t do just what your job description says. I think
occupational therapists should advocate for social change and try to
push that whole area. Sometimes we don’t do it because we don’t feel
it’s our role but if you are looking to improve quality of life then you
have to look at all aspects of it (p 2).
■ Don’t give up or give in. In a study that examined a client definition
of client-centred care (Corring 1996), one client described the impor-
tance of a service provider who didn’t give up:
She came and she would spend hours with me and she stayed with
me fifteen years, like I’m talking about whenever I needed her I
would call her except at home. You know if somebody finds once in
their history somebody who cares that could make all the difference.
Cause what happened, when she started telling the staff that I was
really sick they started believing me, then they found out about my
thyroid and liver disease, they all started apologizing to me. Now for
somebody to believe me after all those years, that’s when I started
getting well . . . (p 76).
■ We need to really listen, even when, and especially when, the client is
in the midst of an illness exacerbation. As one client in Corring’s
(1996) study stated:
When I’m less well I’m less capable of making rational choices, when
I’m at my worst, in my very worst, in the psychosis, I still am capable
of some rationalization and it’s like [other client’s name] said
himself even in psychosis there’s an element of reality there and you’re
still connected to other people when you’re really ill. I’m still capable
of having input, even when I’m really ill and I want that chance,
it’s my life, I don’t want people running it for me. Give me the
atmosphere where I can handle my own life and let me take off with
that, give me my independence, my dignity, my pride cause I’ll fight
you for it if you don’t give it to me, I’ll damn well take it and I
think if we have that pride and dignity we’re running our own lives
(p 75).
■ We have to recognise that time alone may be a good and valued
thing (see Emerson et al 1998 cited above). Just as many of us enjoy
solitude and time out, so do our clients. We have been taught that
one of the ‘problems’ of persons with a mental illness is their lack of
social skills and the experience of social isolation. We need to follow
their lead of when and how much social life they want, need and can
manage.
■ Similarly, we have to recognise that the client has priorities, which may
take precedence over what others think they should be doing. In order
to do that, we have to give up the traditional control/authority of a
professional. The achievement of a balance of authority is central to
client-centred care but is difficult to accomplish (Mishler 1986).
Ask, listen and learn 119
■ We need to look for creative ways for clients to tell us what they know
and what they want. For example, one student, while collecting data
for a qualitative study looking at the life story of a woman living with
schizophrenia (Labbe & Corring 2003) found that the client was
uncomfortable in discussing the signs and symptoms of her illness.
Recognising the importance of a doll that the client cared for like a
child, she asked the client to describe her illness to her doll. The client
was then able to tell the story of her illness without experiencing the
distress that she had felt previously. This not yet qualified, but extremely
intuitive, occupational therapy student had creatively called upon her
observations of the meaning of the relationship of the doll to the client
to assist her in telling her story in a way that she found less stressful.
Box 8.3 Resources for implementing client-centred care in your agency and practice
International Association It is suggested that you, as an individual, or your agency/programme join
of Psychosocial the International Association of Psychosocial Rehabilitation Services
Rehabilitation Services (IAPSRS). The Association’s membership entitles you to a subscription to the
Psychiatric Rehabilitation Journal, newsletters and discounts on texts,
reprints and evaluation tools. Contact details are: International Association
of Psychosocial Rehabilitation Services, 601 N Hammonds Ferry Road, Suite
A, Linthicum, MD 21090-2412, USA; Phone (410) 789-7054, Fax (410)
789-7675; E-mail: membership@iapsrs.org; website: www.iapsrs.org.
CONCLUSION
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123
Chapter 9
Physical disabilities: meeting the
challenges of client-centred practice
M. Gage
CHAPTER CONTENTS
Introduction 123 The interactive planning process 131
Seven dimensions of care 123 Situations that challenge client-centred
Why is it so difficult to implement practice 142
client-centred care? 125 Conclusion 144
The synergistic relationship 126
The issues that arise when interacting with clients who have physical
disabilities differ from those in other health settings. This chapter
outlines the process of building a solid foundation on which to base
a synergistic relationship with the client, and describes how the
interactive planning process can be used to determine realistic goals
based on client-desired outcomes.
INTRODUCTION
tice methods against this measuring stick. The term client-centred is suf-
ficiently vague that it can be interpreted differently by different people.
Hence, it is important to be aware that your peers and your clients may
be using the same term but with different meanings and expectations.
Researchers at the Picker Institute in Boston investigated the experiences
of medical and surgical clients and identified the following seven dimen-
sions as key ingredients to a client-centred experience from the perspective
of the client (Gerteis et al 1993):
■ respect for clients’ values, preferences and expressed needs
■ coordination and integration of care
■ information, communication and education
■ physical comfort
■ emotional support and alleviation of fear and anxiety
■ involvement of family and friends
■ transition and continuity.
The seven themes were initially identified through a series of surveys
of clients at hospitals across the United States. The themes have since
been validated in studies in Canada and the UK (Bruster et al 1994,
Charles et al 1994). Hence, regardless of the health system in which you
are working, it appears that attention to these seven dimensions of care
is critical, from the perspective of clients with physical health problems,
to experiencing client-centred care. Furthermore, it is important to rec-
ognise that these dimensions of care have withstood the test of time in
that, although they were first published in the early 1990s, they continue
to be the gold standard against which care is measured (Institute for
Alternative Futures 2004). It is beyond the scope of this chapter to deal
with each of these themes in detail. However, it is recommended that
individual therapists review the work of Gerteis et al (1993) to determine
the degree to which their current practice is client-centred from the per-
spective of the client. The interactive planning process, which will be
presented later in this chapter, was designed with the express intention of
maximising the client-centred experience by attending to the seven dimen-
sions of care.
The document ‘Vision summit on patient-centered care’ (Institute for
Alternative Futures 2004) states:
For more than two decades, leading health organizations, institutions,
researchers and public policy advocates have promoted the idea that
patients should be at the center of their own healthcare experience. Much
has been learned about the principles and practices shaping patient-
centered care. While many agree that patients should be the focal point
of design and delivery of healthcare, implementation lags. Patient-
centered care is not standard practice in hospitals, nursing homes and
medical practices in the U.S., Canada or Europe. It is still a visionary
goal to be pursued and a set of principles with the power to transform
healthcare. The Picker Institute, a leader in advancing the practice of
patient-centered care, is asking those who work in this field to commit
to a shared vision and take the bold steps to make it the universal
standard of care (p 1).
Physical disabilities: meeting the challenges of client-centred practice 125
Kizer (2002) asserts that ‘modern healthcare is the most complex activity
ever undertaken by human beings’ (p 117). According to Kizer, health
care requires the application of complex technology that has the power
to heal (or to harm, if applied incorrectly). Kizer states that over 80% of
the care is provided by non-physicians with a myriad of different disci-
plines focusing on only one aspect of the overall care of the individual
client. The resultant interactions are complex and multifaceted, and need
a process of coordination that is satisfactory to the client and the provider,
while ensuring the integrity of the procedure being applied. This is a social
process that is acted upon by cultural, economic and political factors. The
emphasis in training of healthcare workers is on the technical aspects of
their respective disciplines, with insufficient time being spent on educating
the individual workers with respect to the interaction with the client or
other members of the healthcare team.
A review of recent literature illustrates that there is much effort being
expended toward achieving the goals of client-centred care, within both
the discipline of occupational therapy and health care as a whole. Studies
continue to support the assertion that more involvement on the part of
the client equals more satisfaction and better outcomes (Grosset & Grosset
2005, Suarez-Almazor 2004, Ward et al 2003). However, other studies
are finding that paternalism is alive and well, to varying degrees, in our
interaction with clients (Pellatt 2004, Rogers et al 2005).
Wilkins et al (2001) researched the reasons for occupational therapists’
difficulty implementing client-centred practice. Their findings suggest
that there are barriers at the level of the system, the therapist and the
client:
■ at the system level, success is dependent upon support from the top of
the organisation, ensuring that client-centred values are integrated into
the structure
■ at the level of the therapist there is a need for more consistent clarity
regarding what client-centred practice is, on a day-to-day basis
■ at client level, there needs to be more acceptance of individual differ-
ences with respect to how clients wish to participate.
Client-centred care needs to allow for a continuum of possible forms.
The power struggle between the professional and the client needs to
be ended. It is not a question of who is in control; it is a question of how
the skills and abilities of the client and all professionals can be brought
together to create a better outcome than would be possible if each par-
ticipant in the healthcare relationship were working independently. It is a
question of how synergy can be created in the healthcare relationship.
Neither the client nor the professional needs to feel the other is in the
126 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
members of the healthcare team. This chapter will now examine each of
the 12 identified subthemes as they apply to the relationship between a
therapist and client who has a physical health challenge.
Building a solid According to Gage (1997) the process of building a solid foundation
foundation upon which to base a synergistic relationship involves:
■ Seeing the client as a whole, including
– acknowledging the strengths along with the problems
– recognising the impact of the illness on the whole family
– being willing to assist the client in finding help for issues that are
not directly related to the reason for your involvement
– recognising that the client lives with the disease 24 hours a day and
is therefore the expert with respect to his or her illness experience
and symptoms.
■ The client feeling heard. This involves
– deep empathic listening that focuses on understanding the other
person’s experience
– demonstrating that you have heard
– changing your actions to be consistent with the new information
– accepting and attending to issues raised by the client and significant
others in the client’s life
– validating concerns, feelings and symptoms
– accepting expressed desires that are inconsistent with your advice or
position
– believing what you hear from the client.
■ Getting to know each other as people, including
– knowing the client as a person, not just the disease
– being willing to divulge appropriate personal information to the
client.
■ Mutual trust in competence, including
– instilling a sense of competence without misrepresenting or unduly
raising hopes of the client
– health professionals demonstrating a belief in the ability of clients to
use their own strengths to rectify problems or issues themselves.
■ Establishing a listening environment, including
– creating a sense that even as a busy therapist you have time to listen
to the concerns of your clients
– finding creative ways to decrease the interruptions when speaking
with a client about issues that are meaningful to the client.
■ Fostering innovation, including
– finding ways to create an environment in which the client feels safe
enough to shape ideas expressed by the professional or to express
ideas that may be contrary to the ideas expressed by the professional
– avoiding behaviours that limit the possible outcome of the inter-
action to what the professional believes is realistic.
Development of a solid foundation upon which to base a synergistic
healthcare relationship is not a linear process, i.e. it is not something that
one pays attention to only at the beginning of a relationship. Instead each
128 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Establishing a The single most important theme identified by Gage (1997) with respect
common vision to creating synergistic healthcare relationships was the presence of a
common vision between the healthcare provider and the client. This is
understandable when one notes that the setting of goals has been found
to be the single most effective means of ensuring that an outcome is
attained (Locke & Latham 1990). When a goal stretches you to achieve
something that is not a current reality, creative tension emerges. When
the energy of everyone committed to this goal is directed toward resolving
this tension (by resolving the discrepancy between the current reality and
the common desired future state), creative solutions, that would not
otherwise have been found, emerge.
For this reason establishing a common understanding of the desired
outcome of the treatment is essential to gaining excellent therapeutic
outcomes. When the client has a different expectation from the therapist
with respect to the goal of treatment, instead of working together to find
creative solutions, there will be conflict that will decrease the chance of
success. The conflict will not always be expressed in a direct manner and
may manifest itself in a lack of compliance with the instructions of the
therapist.
When compliance becomes an issue, it is important that the therapist
does not label the client as non-compliant. Such labels serve only to pit
the therapist and the client against one another in a power struggle.
Instead, the therapist should assume that something is wrong with the
plan and endeavour to find out what alternative strategy will work. It may
be that the client cannot see the connection between the plan and his or
her desired outcome, or that the actions expected of the client cannot
occur because of other life commitments that are too pressing to ignore.
Explore how the context of the client’s life may result in a need to alter
the plan. For example, if a client is involved in a law suit related to the
course of the disability, he or she may subconsciously, or perhaps even
consciously, be afraid that being seen performing some of the actions
outlined in the treatment plan may jeopardise the case. If the client is also
afraid of never being able to return to work, even if improvement occurs
as a result of the therapy, the settlement may be seen as the only way of
continuing to support his or her family. As long as the client’s desired
outcome is to be seen as totally disabled and the therapist’s desired
outcome is to gain a realistic understanding of the degree of disability,
progress will be hampered. A therapist who works through these issues
with the client openly and honestly, rather than labelling the client non-
compliant, may be able to help the client understand that it is important
to be seen as someone who wants to get well.
There may also be a need to develop a documentation process that
itemises the activities the client is performing because it is an expectation
of the therapeutic process and the client’s response to the activity (i.e.
Physical disabilities: meeting the challenges of client-centred practice 129
pain level during the activity, fatigue after the activity, etc.). Clients
involved in legal cases know that they may be secretly videotaped. If the
videotaped activities appear to be inconsistent with the degree of disability
being claimed, they may negatively affect the outcome of the lawsuit. The
knowledge that this evidence will be seen in context, along with a log of
the amount of time spent performing the activity and resultant pain levels,
may be sufficient to allay the client’s concerns and enable you to develop
a common vision for the outcome of treatment.
The establishment of hopeful desired outcomes is also an important
concept to consider when working with clients with physical disabilities.
Health professionals have been trained to be objective in their evaluation
of the client’s condition and prognosis. The objective evaluations are often
based on the average outcome of clients with similar disabilities. However,
it is important that health professionals recognise that some clients defy
the odds and achieve what is thought to be impossible (Sherr Klein 1997,
Siegel 1993). Clients want to be permitted to maintain their hope for a
miracle or, at the very least, a better than average outcome even when all
evidence points to the situation being futile. A poignant example of this
is related by Gage (1997, p 180) as she reports on the experience of Patti,
a woman who was dying of cancer:
She [Patti] approached an expert on visualisation for assistance but
was refused help because she expressed a desire to use the visualisation
techniques to cure her cancer. Her vision of the future was different
than the vision of the future the professional was prepared to allow. The
visualisation expert was prepared to help her only if she would first
admit that she was going to die and that the techniques would only
increase her comfort during the dying process . . . there was an emphasis
on making the client accept reality, even when doing so removed the
purpose for living. This professional denied [Patti] access to a technique
that may have improved her comfort because he believed it was not
appropriate for her to hope for a miracle. As health professionals we
need to open our minds to work alongside our clients toward hopeful
visions of the future.
For the therapist, it may appear to be a waste of precious time to work
with a client toward the achievement of an outcome that is highly unlikely
to occur. The therapist may need to make choices about the quantity of
help each client receives in order to comply with the budgetary restric-
tions of the employing agency and may be unable to justify working on
hopeful outcomes. In addition, if the therapist believes the outcome
being sought by the client is unattainable, he or she will not be motivated
to spend valuable time and resources attempting to gain that outcome
(Craig & Craig 1974). However, it is usually possible, after understand-
ing a client’s hopeful vision for the future, to break down the steps
toward the vision and begin work on a step that is acceptable and believed
to be attainable by both the therapist and the client. The therapist should
be honest with the client about the chances of attaining the hopeful
outcome, while at the same time making a commitment to work with
the client toward the hopeful outcome, one attainable step at a time. As
130 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
the client gains experience with what is possible for him or her, given the
onset of a physical disability, the client may voluntarily alter the desired
outcome.
Health professionals have a tendency to try to ‘fast forward’ this adjust-
ment process. By allowing the recognition to occur gradually, the therapist
gives the client time to find an acceptable alternative outcome for which
to hope before giving up on the more desirable end-result.
Patti’s therapist was right to avoid giving Patti the impression that
visualisation strategies were likely to cure her cancer. However, instead of
insisting that Patti admit that she was going to die before he would agree
to teach her visualisation techniques, the therapist could have agreed to
help her learn visualisation techniques that would help her improve her
comfort. This would have been an interim goal they could both be moti-
vated to work toward.
Feeling valued It is not enough to listen to the opinions of clients. It is essential that the
opinions be valued and acted upon. When it is impossible to act on
the client’s opinions because they are contrary to good clinical practice
or in some way unethical, it is essential that the rationale for choosing
an alternate strategy is discussed fully with the client. There will be times
when this discussion does not result in client satisfaction, but at least the
client will know that the therapist was not simply ignoring the input.
Having fun The creation of an environment that is conducive to having fun while
working toward desired outcomes is considered important by clients.
Clients often find the therapeutic process to be long and difficult. When
an element of fun is added, it helps to keep the client motivated. When
creating a fun environment, emphasis should be placed on creating fun
that is respectful of the cultural diversity of the population. People’s sense
of humour varies – fun that is offensive to a given individual will create
divisiveness, not synergy. Given that humour is unique to the individual,
every effort should be made to encourage clients to speak up immediately
if they are offended by certain comments. It is also critical that clients do
not perceive that you are making light of the seriousness of the challenges
being faced.
Understanding client The first step in the process is to gain an in-depth understanding of the
concerns and client’s concerns and/or expectations. This step is a critical foundation
expectations piece. Misunderstandings that occur at this stage may create unseen bar-
riers throughout the treatment process (Platt et al 2001). It is important
to explore all of the issues outlined in Table 9.1.
The first time you meet a client it will be impossible to gain full dis-
closure on all the issues outlined in Table 9.1. A complete understanding
of all issues will only emerge over the course of time, as the client under-
stands that the therapist values his or her input and finds the information
shared to be critical to the treatment process. However, it is important
that the therapist attempt to gain a starting level of understanding of these
issues before beginning any other part of the assessment process. Once
132 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
the therapist has demonstrated his or her knowledge through the assess-
ment and treatment process, the power imbalance will increase, thereby
making disclosure even less likely. By seeking information from clients
before beginning the ‘hands on’ assessment process, the therapist sends
a message that the information clients possess about their illness experi-
ence is critical to the process of assessment and treatment. In this way
clients begin to believe that they also have power related to the knowledge
they possess about their illness experience and the context of their life.
Physical disabilities: meeting the challenges of client-centred practice 133
Clinician skills and Given that each individual client has a unique illness experience, different
knowledge knowledge and skills may be required to address the issues and concerns
raised by two clients with the same diagnosis. Once the therapist under-
134 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Document client- The term client-desired outcomes is used to describe the statements that
desired outcomes emerge through an interactive process with the client and become the
focus of treatment and outcome measurement. Client-desired outcomes
are not goals in the usual sense of the word. Generally goals are thought
to be realistic, understandable, measurable, behavioural and achievable
(Saunders 1984). The client-desired outcome is instead a statement of
what the client wants to achieve. It is not limited by what can be measured
in objective, behavioural terms. Nor is it limited by the therapist’s view
of what is realistic. Instead it reflects what the client sees as the desired
future state at the time it is written. The client-desired outcome is also
not ‘carved in stone’. It may change as the client gains more experience
with what is possible given the onset of the physical limitations related to
the illness or disease. As such, the client-desired outcome is written, as if
by the client, in the first person.
The client’s perceived self-efficacy, i.e. the client’s perceived ability to
perform a specific task, is based on efficacy information that is no longer
accurate given the new limitations being experienced (Bandura 1986). As
such, the client cannot be expected to have a realistic sense of what is
achievable. Nor can the client be expected to become ‘realistic’ as soon
as the therapist explains his or her view of what is realistic. There is instead
a need to support the client in experimenting with what is possible, given
the new physical limitations. When the client-desired outcome is consid-
Physical disabilities: meeting the challenges of client-centred practice 135
General hypotheses Clients state that their individual preferences, values and expressed needs
are not being considered when treatment plans are developed (Gerteis et
al 1993). Rogers and Holm (1991) note that therapists begin to generate
their hypotheses about what is wrong and what treatment may be indi-
cated as soon as they read the diagnosis on the chart. This means that
much treatment planning is occurring before there is a true understanding
of the client’s unique illness experience or desired outcomes.
Once the client-desired outcomes have been developed, it is important
to determine whether this new information suggests new hypotheses.
Hypotheses are sometimes so firmly entrenched that they are assumed to
be true for all clients. For example, an occupational therapist heard the
diagnosis spinal cord injury and hypothesised that the injury had impaired
the client’s ability to dress independently and that regaining independence
in dressing would be a desired outcome of the treatment programme. The
process of dressing was so exhausting that this particular client chose to
hire an attendant to assist him with dressing so that he would have energy
136 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
left to do the things that were really important in his life. This client
had wanted to stop the dressing programme much earlier, but was afraid
of hurting the therapist’s feelings if he told her his plan. Many weeks of
valuable treatment time were wasted attempting to resolve issues related
to independent dressing simply because the therapist was working from
the wrong hypothesis. Had she taken the time to explore with the client
the meaning of various occupations, a different hypothesis may have been
used in planning treatment and valuable treatment time would have
been saved.
The hypothesis that all clients want to be independent in dressing was
so firmly entrenched in this therapist’s mind that she did not consider
other possible responses of the client. It is also important to note that
this client’s view of the importance of independence in dressing changed
during the course of treatment. It was only when he experienced the
exhaustion brought on by attempting to dress independently that he
changed his view. This illustrates the importance of remembering that the
interactive planning process is an iterative, as opposed to linear, process.
Provision must be made to facilitate changes in the desired outcomes of
treatment as new information becomes known or, as in this case, the client
gains more experience with the consequences of the disability.
Assess barriers Now that the therapist has a good understanding of what the client is
trying to achieve and what contribution the client is prepared to make, it
is time to begin the process of identifying what stands in the way of the
client’s success. The therapist is expected to use all possible professional
knowledge and skill in an effort to assist the client in achieving client-
desired outcomes and in identifying issues that may be important, but not
apparent, to the client.
The assessment should be streamlined to be consistent with the client’s
desired outcomes. Achieving holistic practice is more an issue of assessing
all aspects of client functioning that are related to client-desired outcomes
than of assessing and treating all possible problems. Having said that, it
is also critical that the assessment encompasses components that are essen-
tial to the identification of important issues about which the client may
have no knowledge.
Being client-centred does not mean attending only to issues raised by
the client. The therapist is trained to understand issues that may arise
within specific diagnostic categories, and thus will have knowledge about
issues that must be shared with the client. Ignoring issues because the
client does not identify them would not be client-centred. However, once
the issue has been identified, if it is still unimportant to the client the
therapist should be prepared to defer to client choice unless the decision
presents a threat to others or the client is not competent to decide. It is
important that the therapist makes every effort to ensure that the client
understands the ramifications of the decision but, ultimately, the therapist
must respect the client’s choice and avoid using professional power to
sway that choice. For example, if during the course of an assessment of a
client who had a broken leg you become concerned about the presence
of a learning disability, you would provide the client with information
about your concerns and possible courses of action. The client who has
adapted to the disability may not wish to pursue assessment and treat-
ment. Provided the client is considered competent to decide, and given
that there is no apparent risk to the client or others, the therapist should
respect the right to refuse treatment.
Validate assessment Once the assessment is complete, it is important to share the analysis of
findings the results with the client to provide a new perspective on the assessment
data. For example, when assessing a client’s ability to return to work, the
therapist might be looking for maximum voluntary effort indicators.
If you identify indicators of inconsistent effort and share these thoughts
with the client, you provide the client with an opportunity to disclose any
fear of reinjury or of bringing on a second heart attack. This provides
an alternative interpretation for the data that may be important to your
conclusions. Platt et al (2001) emphasise the need for healthcare profes-
sionals to be prepared not only to listen to the hypotheses of their patients,
138 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Negotiate specific Now that the assessment is finalised it is time to develop specific treatment
treatment goals goals that are consistent with the client-desired outcomes. These state-
ments will be specific and measurable indicators of the direction of treat-
ment. If the assessment results uncover issues that change the client-desired
outcomes, these should also be modified.
Gain client Once treatment goals are established, the client should be asked to make
commitment a commitment to working toward each goal. The connection between
these goals and the client’s desired outcome should be articulated specifi-
cally so that there is little chance of misunderstanding.
Design and implement Once the client has committed to the goals, the specific action plan to
a specific action plan attain those goals can be developed and implemented.
Evaluate The appropriate time for evaluation will vary from situation to situation
and will be related to the desired outcomes being addressed and the
speed with which individual goals are likely to be attained. When it is
time to evaluate the outcome it is important to ensure that the evaluation
examines whether the client-desired outcomes have been achieved rather
than evaluating whether the goals have been achieved. The biggest
mistake therapists make is to evaluate the effectiveness of the programme
by evaluating the attainment of the goals that were derived in an attempt
to achieve the desired outcomes. The attainment of the specific goals
becomes inconsequential if their attainment does not in turn bring the
client closer to the desired outcomes articulated in the first stage of
the process. The goals were defined by breaking down the desired
outcome into manageable steps. It may be that there was a fault in
the reasoning that led to the selection of a specific goal and, hence, the
attainment of that goal may not result in the attainment of the desired
outcome.
Evaluation can be performed in one of the following three ways:
■ You can use a dichotomous measure of ‘yes’ or ‘no’. In this case you
would ask the client: ‘Has this outcome been accomplished to your
satisfaction?’ The client would answer ‘yes’ or ‘no’. The success of
treatment would be dependent upon how many ‘yes’ responses were
achieved. It is appropriate for the client to answer ‘yes’ to a question
when it is about an outcome that has become irrelevant during the
course of treatment. It is also acceptable for this outcome simply to be
removed from the list, and considered to be accomplished, at the time
it becomes irrelevant during treatment. There is no sense continuing
to work on outcomes that have been resolved in terms of importance
to the client.
Physical disabilities: meeting the challenges of client-centred practice 139
Case example The following is a case example applying the interactive planning process
to a client.
■ The client: A 66-year-old woman who has recently undergone a knee
replacement. She has just been discharged to her home and is being
seen by an occupational therapist in her home for the first time.
■ Client’s concerns/expectations: Using the enabling interview, the occu-
pational therapist discovers that this woman, Norma, has a lifelong
passion for gardening. The plants she nurtures are given away to people
she cares about as a sign of her love and she is terrified that she will
never be able to garden again. She has two grown children who live a
long distance away. She hates the idea of having people invade her
home to assist her with her personal care but is willing to consider some
assistance with heavy housework. At this point the client is only willing
to consider return to her pre-hospitalisation lifestyle as the desired
outcome of her work with the occupational therapist. Norma believes
that her knee problems are the result of the long hours she spends
kneeling in the garden.
■ Clinician skills/knowledge: The occupational therapist, Sara, believes
that she can help Norma with many of the life activities that she needs
to accomplish if she is to live without the support of a personal care
attendant but is concerned that her knowledge of gardening is
insufficient.
■ Desired outcomes: After negotiation between client and therapist the
following desired outcomes are documented:
– I want to live independently with the exception of having someone
come in to do the heavy housework once per month
– I want to be able to garden the way I did before my knee problems
started.
Sara is not certain that she can bring Norma to this level of function
but she knows that she can bring her toward each of these desired
outcomes. She honestly and openly lets Norma know that she thinks
they will have to set their sights a little lower to begin with but that
the initial steps will move her closer to her desired outcomes.
Physical disabilities: meeting the challenges of client-centred practice 141
mines that there are none. She uses a list serve on the internet to
gain information from expert therapists about appropriate sources of
information. She is put in touch with people and resources that
appear to be appropriate to this client.
– Norma’s role: To help Sara understand which strategies were effec-
tive in helping her to learn new things prior to the knee replacement;
to be the expert on gardening and to help Sara to understand what
her strengths and barriers are with respect to returning to gardening;
to evaluate the potential effectiveness of strategies that Sara presents
that may help her to move toward her desired outcomes.
■ Goals:
– Norma will be able to don and doff lower extremity clothing using
appropriate devices within 1 week. (Plan: acquire devices; train in
usage; evaluate effectiveness.)
– Norma will be able to manage container gardening activities at
worktable in greenhouse within 2 weeks. (Plan: evaluate access to
greenhouse; adjust worktable height; acquire equipment; attempt
activity.)
■ Implementation and evaluation: Sara and Norma will both do their
respective tasks and meet in a week to determine efficacy. Sara to have
done COPM scoring with respect to desired outcomes and to re-
evaluate after qualitative information indicates change has occurred.
■ Next step: This depends upon whether the evaluation indicates success
(full or partial) or not. If the strategy is successful and Norma has
moved toward the desired outcome, then the next step in the plan can
be developed. When one is successful with goal attainment there is no
need to re-evaluate whether you have moved along the right path.
However, if the strategy is unsuccessful it is important to start back at
step one to determine if the reason for failure is due to inappropriate
assumptions in the earlier stages. For example, if Norma proves to be
unable to learn the new strategies using the techniques that worked for
her previously, perhaps there should be a re-evaluation of the assump-
tions made earlier.
When the desired outcomes of family members are different from those
of the competent client, it is important to attempt first to find a synergistic
solution that will satisfy the needs of all involved parties. It must be rec-
ognised that the family member may be as affected by the choice being
made as the client. The client does not live in a vacuum and a client’s
choice may have significant effects on family members. The client is, in
effect, part of a system: when one part of the system changes, effects are
felt on other parts of the system. Failure to consider these effects may
lead to a poor decision, and thence to a poor outcome. First, try to
understand the concerns of each participant and what they are attempting
Physical disabilities: meeting the challenges of client-centred practice 143
Dealing with Therapists encounter situations where the client’s desired outcomes
moral dilemmas conflict with the beliefs of the therapist. For example, the therapist may
be asked to provide treatment to enable a client to accomplish a desired
outcome that the therapist considers to be unsafe. Provided the client is
competent and the outcome is not endangering others, is not illegal or
morally corrupt, the therapist may have an obligation to allow the client
to ‘live at risk’. Laws regarding such choices are regionally different. Thus,
therapists should endeavour to understand the laws governing their
practice environment and seek legal counsel when in doubt.
Morally challenging situations require that therapists, in order to
protect themselves from litigation, seek advice and support from col-
leagues. When placed in a situation where they believe they are assisting
a client to harm him/herself, there is a need to seek help to deal with the
emotional consequences to the therapist.
When the moral dilemma relates to a client wishing to engage in an
activity that challenges the therapist’s moral standards, the therapist should
attempt to find an alternative source of help for the client. For example,
a client who wishes assistance with positioning in order to engage in pre-
marital sex may encounter a therapist opposed to premarital sex. It is
important that therapists do not attempt to force their moral position on
to the client. Instead, the therapist should refer the client to another
occupational therapist for whom this moral dilemma does not exist.
When you are part It is possible for one member of a team to use the interactive planning
of a team process to plan his or her aspects of treatment without commitment from
all team members. When at least one member of the team is using
this process, that team member can advocate for the client’s perspective
within team meetings. It is preferable, when there are multiple team
members, that the interactive planning process be used by the whole
team. In this way the opinions and skills of all members of the team,
including the client as a significant member of the team, are taken into
consideration.
Gage (1994) presents a strategy for coordinating the work of the team
around the desired outcomes identified by the client. Essentially, one
member of the team acts as a primary contact with the client to begin the
interactive planning process. One set of desired outcomes that are accepted
by all team members is developed. Each member of the team then inter-
acts with the client to determine the unique role of that discipline with
respect to attaining the client’s desired outcome.
144 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
CONCLUSION
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147
Chapter 10
Client-centred practice in paediatrics
D. Stewart, D. Cameron
CHAPTER CONTENTS
Background 147 Challenges and strategies to implementation of
Client-centred practice with children 148 CCP and FCS 153
Family-centred practice 148 Conclusion 157
Client-centred assessment and intervention in
occupational therapy 150
BACKGROUND
For the purposes of discussion in this chapter, the field of paediatrics refers
to services provided to children and adolescents up to the age of 21 years.
Occupational therapists have worked with this population for many years.
They are involved with children and adolescents with a variety of chal-
lenges including physical, cognitive, sensory and affective in a variety of
settings including hospitals, schools, daycares, homes and communities.
In Canada, the Canadian Association of Occupational Therapists (CAOT)
indicates that, of the members who completed the survey, 5.8% work at
least in part with neonates, 19.9% with preschoolers, 29.4% with school-
age children and 31.5% with adolescents (CAOT 2004). Therapists were
asked to indicate all populations that describe their clinical practice. In
148 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
FAMILY-CENTRED PRACTICE
service recognizes that each family is unique; that the family is the
constant in the child’s life; and that they are the experts on the child’s
abilities and needs (Law et al 2003a, p 2).
■ providing sufficient education to the child and family so that they can
make informed decisions
■ facilitating the child and family to participate in the goal-setting process
■ developing service plans with parents that present a range of options
■ encouraging the child to make choices of intervention activities within
sessions
■ assisting parents to encourage their child to make informed decisions
within the family context at an early age.
The Canadian The COPM (see Ch. 11) is a semi-structured interview designed to help
Occupational Performance clients identify problems in occupational performance (Law et al 2005).
Measure (COPM) Children are usually able to complete the COPM once they are chrono-
logically or developmentally about 8 years of age. Once the child has
identified issues in their occupational performance, they rate, on a 10-
point scale, their goals in terms of importance, satisfaction and perform-
ance. Reliability and validity for the COPM have been demonstrated.
Perceived Efficacy and The PEGS (Missiuna et al 2004) is designed to enable young children
Goal Setting (PEGS) with disabilities to self-report their perceived competence in everyday
activities and to set goals for intervention. It provides a method for chil-
dren who are too young to be able to respond to questionnaires and other
survey instruments to articulate what they would like to work on in
therapy. The PEGS is most appropriate for children who are chronologi-
cally or developmentally at a 6- to 9-year-old level. By using the PEGS
with the child, therapists can truly practise from a client-centred philoso-
phy and give a voice to even very young children. Teacher and caregiver
questionnaires with comparable items to the child questions are
available.
Paediatric Activity Card The PACS (Mandich et al 2004) is a measure designed for use with chil-
Sort (PACS) dren between the ages of 5 and 14 years to help determine the occupa-
tional repertoire of children at a particular point in time. The PACS
consists of a series of actual photographs depicting children of various
ages engaged in 75 different activities that include personal care, school/
productivity, hobbies/social activities and sports activities. There are also
blank cards that allow the child to talk about activities that are not
captured in the pictures. Using the PACS to discuss activities the child
would like to do makes it a useful instrument for understanding the activ-
ity limitations of the child. The PACS can be administered once, to gain
an occupational profile, repeatedly to gain an occupational trajectory, or
pre- and postintervention to capture intervention effects.
152 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Sensory Profile There are some assessments that are not specifically designed to be admin-
istered to younger children but the therapist might want to take the
opportunity to use the assessment with both parent and child. One of the
authors of this chapter has used the Sensory Profile (Dunn 1999) with
both parent and child. This questionnaire in its expanded form is quite
lengthy and some of the language needs to be modified for children but
it appears that it can be used with children from about the age of 9–10
years. The children have enjoyed completing the same assessment as their
parent, the parents have found it very interesting to compare their per-
ception with their child’s, and the therapist has found it beneficial to
have two different perspectives on the sensory issues. There is also an
adolescent/adult version of the Sensory Profile, which teenagers enjoy
completing by themselves (Brown & Dunn 2002).
Cognitive Orientation to The CO-OP intervention approach guides children to discover cognitive
Occupational Performance problem-solving strategies that can be directly applied to occupational
(CO-OP) performance of tasks chosen by the child (Polatajko et al 2001). CO-OP
intervention also uses cognitive scaffolding, adult guidance and feedback
as well as motor learning and motor control theories (Polatajko et al
2001). The main objectives of CO-OP include skill acquisition, cognitive
strategy development, generalisation and transfer. CO-OP is usually deliv-
ered over 12 one-to-one sessions with five phases (preparation, assess-
ment, introduction, acquisition and consolidation). Within these sessions
children are taught to use two types of strategy: a global problem-solving
strategy (goal, plan, do, check) and domain-specific strategies to enable
them to perform their chosen activities (Polatajko et al 2001). CO-OP
adopts a ‘top-down’ approach that focuses on occupational performance
as an outcome. Its aim is to change the child’s skill level and enable them
to perform their motor-based goal in a way that works best with their
Client-centred practice in paediatrics 153
Family-centred Principles of dynamic systems theory have been incorporated into another
functional therapy new intervention approach called family-centred functional therapy
(FCFT). In this approach, the therapist asks the parent to identify motor-
based tasks that the child is having difficulty with. The therapist’s role is
to work with the parents and child to identify factors in the task, the
environment and/or the child that are impacting on the child’s perform-
ance of the chosen task (Law et al 1998). Treatment will only begin if
the child is motivated to work on the task and when constraints have been
identified for which treatment can be provided.
Intervention focuses on changing impediments in the environment
and with the task since these are often most amenable to change. For
constraints that are child-specific, they will only be addressed if the issue
is specific and changeable with time-limited hands-on treatment such as
positioning. However, the primary intervention is to adapt the task or
change the environment rather than focusing on changing deficits in the
child. The effectiveness of FCFT has been demonstrated with young
children who have cerebral palsy in several studies to date (Darrah et al
2001, Law et al 1998b, McGibbon Lammi & Law 2003).
System challenges A major barrier to implementing client-centred practice comes from the
and strategies traditional ‘ways of doing’ in paediatrics. The medical model views the
professional as the expert, who ‘fixes’ a client’s problems; institutional
systems and practices often utilise this traditional model of service delivery.
Unfortunately, the concept of client-centred services doesn’t fit with
these views and practices. Most experts agree that it is not a matter of
‘adding on’ a CCP or FCP approach, as the lack of fit with traditional
service delivery makes this impossible (Lawlor & Mattingly 1998). A shift
in attitudes and beliefs about families, power and practice is required at
both individual and system levels in order to bring these new approaches
into practice. Administrative support is required to provide therapists and
other service providers with time for training and policy development.
Parents need to be included on boards, committees and other institutional
structures to effect a positive change.
Change takes time, and requires a commitment from everyone involved.
A lack of time is often cited as a barrier to implementation of CCP. As
discussed in other chapters in this book, although client-centred practice
154 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
may take more time to implement initially, in the long term it should be
less time consuming as clients take more responsibility for making deci-
sions and addressing issues (see Ch. 1).
Strategies and guidelines for becoming more family-centred are availa-
ble online from numerous organisations (Beach Center on Disability
2005, Law et al 2003a). Some of the key strategies for services include:
Who is the client? In Chapter 1 of this book, Thelma Sumsion notes that the concept of
‘client’ has to be broadened to include family members and significant
others when working with children. The family-centred service literature
has guided therapists to recognise the whole family unit as the primary
client in paediatric services. This creates challenges for service providers,
as the number of issues broadens and tensions emerge about whose per-
spective, goals and needs should be considered most important (Lawlor
& Mattingly 1998). Furthermore, in today’s multicultural societies, thera-
pists need to consider diverse family situations, backgrounds, views and
child-rearing practices if they are working in partnership with families
(Ochieng 2003). Generic strategies for training and skill development
needed by therapists working within a CCP include cultural sensitivity,
communication and negotiation skills, shared goal setting and teaching/
educational theories about ‘giving’ information effectively to different
people (Hanna & Roger 2002, Law et al 2003c).
Case study 1 provides a scenario which describes how an occupational
therapist solves the challenge of who is the client.
There are some specific challenges and strategies facing paediatric occu-
pational therapists related to the issue of identifying ‘who is the client?’.
These include the age of decision-making, client insight and school system
challenges.
Age of decision-making One of the client issues that is specific to the paediatric population relates
to the age at which children can make their own decisions. Although the
legal and legislative requirements for informed consent and decision-
making vary among countries, many do not identify a specific age but
rather recognise that a child can give informed consent for health care
provided he or she can understand the information about the services and
risks involved (Morton & Westwood 1997). The responsibility rests with
the service provider to determine a child’s capacity to make an informed
decision. Within a family-centred approach, this responsibility would be
shared with the family. The role of the therapist is to provide as much
information as possible, in a form that is understandable by all family
members including the child, in order to promote shared decision-making.
156 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
Client insight Another client issue that often emerges within the developmental nature of
paediatric practice is client insight into occupational performance issues or
problems. Children at different ages and stages may not be able to identify
their own goals or needs, especially if they have not been encouraged to do
this within their family. Therapists may therefore have to try different strate-
gies to promote a child’s own identification of issues. For example, the use
of the PEGS measure (Missiuna et al 2004) helps a school-aged child to
identify their own competencies and set goals instead of identifying ‘prob-
lems’. Some children and adolescents do not see the word ‘problem’ as per-
sonally relevant (‘I’m fine!’) and other words, such as ‘issue’ or ‘things you’d
like to do or change’ may need to be used to determine occupational per-
formance issues from a young person’s perspective.
The client in the A third challenge related to ‘who is the client?’ in paediatrics is identified
school system by therapists who work in the school system. Some service delivery models
have occupational therapists providing their services to children in schools,
and the family is not actively involved due to policies and funding struc-
tures. Therapists provide consultation, information and support to school
personnel, and often consider them to be their ‘clients’. Family-centred
service approaches recognise that multiple people outside of the immedi-
ate family are involved in the ongoing care and support of children with
special needs, including school personnel and community members. An
FCS approach considers all perspectives, as they often differ. A study by
Pollock and Stewart (1998) that asked school-aged children, parents and
teachers to complete the Canadian Occupational Performance Measure
found that each group identified different occupational performance
issues and priorities. An occupational therapist must use skilled commu-
nication and negotiation skills to determine the best course of action given
these multiple perspectives.
CONCLUSION
young persons that their family, other caregivers and service providers will
be intimately involved in their lives. Hence, occupational therapists must
view the concept of ‘client’ in a broad sense to include these significant
people. The principles of client-centred practice can be applied in all stages
of paediatric practice, and these principles are congruent with the assump-
tions and principles of family-centred service, which has become the primary
approach to service delivery in paediatrics in the past few decades.
The most significant challenge facing occupational therapists working
in paediatrics relates to the issue of ‘who is the client?’. A broadened defi-
nition of client, to include the family and significant others in a young
person’s life, makes it difficult for a therapist to know who is the primary
focus of service. Recent developmental models and research, however,
provide some support for viewing the child–parent relationship as a
dynamic unit. Furthermore, the family unit exists within a social context,
which also must be considered. This dynamic and interactive view of
children and families fits with current occupational therapy models of
practice, which acknowledge the transactive nature of person, environ-
ment and occupation fit (e.g. Baum & Christiansen 2005, Law et al
1996). When occupational therapists view the child and family as the focus
of services, their primary functions are to educate others by sharing their
expertise and information to enable all ‘clients’ to make informed deci-
sions which will ultimately enable a child’s occupational performance and
well-being.
References
Law M, Mills J 1998 Client-centered occupational Mayer M L, White B P, Ward J D, Barnaby E M 2002
therapy. In: Law M (ed) Client-centered Therapists’ perceptions about making a difference in
occupational therapy. Slack, Thorofare, NJ, p 1–18 parent–child relationships in early intervention
Law M, Cooper B, Strong S, Stewart D, Rigby P, occupational therapy services. American Journal of
Letts L 1996 The person–environment–occupation Occupational Therapy 56:411–421
model: a transactive model to occupational Missiuna C, Pollock N, Law M 2004 Perceived efficacy
performance. Canadian Journal of Occupational and goal setting (PEGS) manual. Psychological
Therapy 63:9–23 Corporation, San Antonio, TX
Law M, Darrah J, Pollock N et al 1998 Family- Morton W J, Westwood M 1997 Informed consent in
centred functional therapy for children with children and adolescents. Paediatrics and Child
cerebral palsy: an emerging practice model. Physical Health 2:329–333
and Occupational Therapy in Paediatrics 18: Murray R B, Zentner J P 1997 Health assessment and
83–102 promotion strategies through the life span, 6th edn.
Law M, Rosenbaum P, King G et al 2003a What is Appleton and Lange, Stamford, CT
family-centred service? (FSC Sheet #1). CanChild Ochieng B M N 2003 Minority ethnic families and
Centre for Childhood Disability Research, family-centred care. Journal of Child Health Care
Hamilton, ON. Online. Available: www.canchild.ca 7:123–132
Law M, Rosenbaum P, King G et al 2003b How Polatajko H, Mandich A, Miller L, Macnab J 2001
does family-centred service make a difference? Cognitive orientation to occupational performance
(FSC Sheet #3). CanChild Centre for Childhood (CO-OP) part II: The evidence. Physical and
Disability Research, Hamilton, ON. Online. Occupational Therapy in Pediatrics 20(2/3):83–106
Available: www.canchild.ca Pollock N, Stewart D 1998 Occupational performance
Law M, Rosenbaum P, King G et al 2003c Becoming needs of school-aged children with physical
more family-centred. (FCS Sheet #5). CanChild disabilities in the community. Physical and
Centre for Childhood Disability Research, Occupational Therapy in Paediatrics 18:55–68
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Law M, Baptiste S, Carswell A, McColl M, Polatajko Family-centred service: a conceptual framework and
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Performance Measure, 4th edn. CAOT Publications in Pediatrics 18:1–20
ACE, Ottawa Stewart D, Harvey S 1990 Application of the
Lawlor M C, Mattingly C F 1998 The complexities guidelines for client-centred practice to paediatric
embedded in family-centred care. American Journal occupational therapy. Canadian Journal of
of Occupational Therapy 52:259–267 Occupational Therapy 57:88–94
McGibbon Lammi B, Law M 2003 The effects of Viscardis L 1998 The family-centred approach to
family-centred functional therapy on the providing services: a parent perspective. Physical and
occupational performance of children with cerebral Occupational Therapy in Pediatrics 18:41–53
palsy. Canadian Journal of Occupational Therapy Watson D 1992 Documentation of paediatric
70:285–295 assessments using the occupational therapy
Mandich A, Polatajko H J, Miller L T, Baum C 2004 guidelines for client-centred practice. Canadian
The Paediatric Activity Card Sort. CAOT, Ottawa Journal of Occupational Therapy 87:87–94
161
Chapter 11
The Canadian Occupational
Performance Measure
N. Pollock, M. A. McColl, A. Carswell
CHAPTER CONTENTS
Outcome measurement 161 Research applications of the COPM 166
Description of the COPM 162 Clinical applications 167
Development of the COPM 164 Case examples 170
Psychometric properties of the COPM 165 Conclusion 174
OUTCOME MEASUREMENT
Implement plans 4
through occupation Identify strengths
and resources
Negotiate targeted
outcomes and develop
action plans
164 CLIENT-CENTRED PRACTICE IN OCCUPATIONAL THERAPY
pational performance problems. This is the step where the COPM can
be used initially. It allows the client to express the areas of concern in
daily occupational performance and to indicate the priority of those con-
cerns. From there, the therapist selects a theoretical perspective and
moves to a second level of assessment, seeking to understand why the
client is experiencing the problems identified. These steps include assess-
ing performance components, examining the environment, and identify-
ing strengths and resources within the client or the client’s situation. The
COPM is not designed to be used in these steps. It is targeted at under-
standing the presenting occupational performance problems from the
client’s perspective. There are many other tools and methods available to
assist in the completion of steps 3 and 4 of the occupational performance
process.
Once a plan has been formulated and implemented (steps 5 and 6),
the final step is to evaluate outcomes. Again, this is where the COPM can
be used. Clients can score their performance and satisfaction with per-
formance in the areas identified through the COPM completed in step 1.
The COPM can be used at the beginning and at the end of the occupa-
tional performance process.
The COPM is a standardised instrument, in that there are specific
instructions and methods for administering and scoring the test; however,
it is not a norm-referenced measure. It was not designed to assess devia-
tions in occupational performance from some empirically driven norm. In
fact, no such norm exists and, even if one did, it would be inconsistent
with the theoretical basis of the COPM to apply a population-based
standard to occupational performance. The theoretical base upon which
the measure was developed describes occupational performance as an
individual, subjective experience.
The initial development and pilot testing of the measure were completed
in several phases and involved occupational therapists and clients from 55
test sites in Canada, Britain, New Zealand and Greece (Law et al 1994a).
Since that time, the use of the COPM has exploded. It is now used in 35
countries and has been translated into more than 20 different languages.
In the years since its initial publication, the body of literature about the
COPM has grown substantially. A recent critical review of the COPM
literature found 88 published papers (Carswell et al 2004).
Utility The results from several studies show that the majority of COPM users
found it easy to administer. The typical time to complete the COPM was
20–40 minutes (Law et al 1994b, McColl et al 2000, 2006, Toomey
et al 1995). The time taken to administer the COPM is influenced by
whether the therapist and client stick to assessment; if they begin to
analyse and solve the problems identified, the administration time is then
lengthened. Therapists report that the COPM has helped them to engage
clients in the therapeutic process, to set appropriate goals and to evaluate
change (Carswell et al 2004). Another benefit frequently reported by
occupational therapists who use the COPM has been that it helps to clarify
the role of the occupational therapist with the client and other team
members (Chen et al 2002, Fedden et al 1999, Toomey et al 1995).
From the client’s perspective, most found that the COPM helped them
to define their occupational problems more clearly, to consider their per-
sonal priorities and to understand the role of occupational therapy (Waters
1995, Wressle et al 2002). Some clients were not used to identifying their
own problems for intervention and found the process overwhelming;
others had difficulty shifting their expectations from therapist as expert to
client as expert. For some, however, this was very empowering and they
enjoyed the opportunity to become a partner in their own rehabilitation
(Law et al 2005).
The recent review of the COPM literature demonstrates the broad
applicability of the tool (Carswell et al 2004). Studies have reported the
use of the COPM with a wide variety of clients in numerous different
settings including those with physical and mental health issues, all age
groups from neonates to the very old, as well as clients in hospital, out-
patient and community settings, including those who are homeless.
Responsiveness Responsiveness refers to the ability of the COPM to detect change over
time. Responsiveness was originally evaluated as part of the pilot study,
and results showed significant differences between initial and reassessment
scores for both performance and satisfaction scores (P < 0.0001, df = 138)
(Law et al 1991). Since then, six other studies have tested the responsive-
ness of the COPM (Bowie et al 1999, Carpenter et al 2001, Chen et al
2002, Lewis & Jones 2001, Sanford et al 1994, Wressle et al 1999). The
consensus from these studies is that the COPM is very responsive to
change in both the performance and satisfaction scales and in comparison
to other measures.
Validity Content validity of the COPM is supported by the process through which
it was developed (Bosch 1995). In addition, the COPM has come to
represent a standard for measurement in research, practice and education
in occupational therapy as evidenced by the conference presentations,
citations and translations into other languages (Baptiste et al 1993,
Steeden 1994, Trombly 1993). More recent studies have continued to
support the use of the COPM as a valid measure of occupational perform-
ance (Carswell et al 2004).
Criterion validity has been assessed by comparing COPM scores with
scores achieved on measures of a similar construct. Measures that focus
on quality of life, the impact of disability and functional performance tend
to be the most strongly correlated with the COPM (Bosch 1995, Boyer
et al 2000, Carpenter et al 2001, Law et al 1998, Lewis & Jones 2001,
McColl et al 2000). Measures that have a narrower focus or are more
targeted at the impairment level, not surprisingly, show lower correlations
(Chan & Lee 1997).
In summary, the evidence available to date indicates that the COPM
is a clinically useful measure with wide applicability, having adequate to
high test–retest reliability, significant responsiveness, and good content
and criterion validity.
One of the most exciting advances in the past 10 years in the field of occu-
pational therapy has been the growth of the body of effectiveness evidence.
Many of the studies published in the field have used the COPM as one of
their primary outcome measures. Client populations have included children,
adults and seniors, and those with neurological, musculoskeletal, respiratory
and psychological conditions, both acute and chronic in nature. Therapeutic
approaches evaluated include programmes of occupational therapy for par-
ticular client groups and more targeted interventions such as botox injec-
tions for reduction of spasticity, powered mobility, splints, virtual reality and
client education programmes. These studies have provided evidence of the
The Canadian Occupational Performance Measure 167
CLINICAL APPLICATIONS
clients’ concerns and none of the therapists asked the clients to establish
priorities of concern. The gap between self-reported actions and observed
actions seems very significant. These studies serve to show the difficulties
some therapists are experiencing in trying to operationalise some of the
basic principles of client-centred practice.
While the COPM can facilitate a client-centred relationship, this is
rarely a simple thing to accomplish. Where a client can clearly articulate
his or her occupational performance concerns and priorities, administra-
tion of the COPM is easy. However, for the majority of clients seeking
occupational therapy services, eliciting a list of priority problems will be
more challenging. Clients may have cognitive impairments which limit
their insight or ability to understand the COPM. They may speak a dif-
ferent language or have a communication difficulty which limits their
ability to respond. They may be experiencing significant emotional turmoil
and have difficulty in decision-making or simply be unused to being asked
for their opinion in a healthcare context.
There are many factors that will increase the difficulty in using the
COPM and place greater challenges on the therapist. It is then incumbent
on the therapist who wishes to remain true to a client-centred approach
to be creative in gaining the required information. Some clients simply
need more time to think about the questions or more time to respond.
Some will require the development of a more solid relationship with the
therapist first. They may require a higher level of trust to develop before
feeling comfortable in responding. For some, the process may need to be
made more concrete, for example walking through a typical day’s schedule
with the client to help them describe areas of occupational performance
that are more disrupted or more important to them. Some clients may
need more help in understanding the rating scales or more examples of
things we typically rate to help them use the scales in a meaningful way.
For some clients, for example young children or those with significant
cognitive impairment, the COPM will need to be done with family or
caregivers rather than with the clients themselves. Here it is important to
emphasise that the respondent is describing his or her own perspective
and not answering as a proxy for the individual client. For example, the
mother of a young child with cerebral palsy is being asked how important
it is to her that the child can learn to dress him- or herself, not how
important it is for the child. Respondents cannot truly know how someone
else feels and, therefore, can really give only their own perspective. It is
also important that the therapist initially gives the client the benefit of the
doubt and tries the COPM with them. Many therapists have reported
being surprised by the level of insight of particular clients whom they
anticipated would be unable to respond to the COPM.
There are times when the therapist will question the information
received from the client; this is particularly an issue if the therapist consid-
ers that the client is at risk. For example, an elderly client living alone may
not perceive that she is having any difficulties around the home, but the
therapist may believe her to be at high risk for falling. Here the therapist
may need to take a more directive approach in pointing out her concerns
to the client and working towards a solution. Wherever possible, input
from family and/or caregivers may be helpful in resolving these types of
The Canadian Occupational Performance Measure 169
that it is the philosophy and the skills of the therapist, rather than the
types of client or practice settings, that determine whether the COPM is
used successfully (Bodiam 1999, Cresswell 1998, Fedden et al 1999, Mew
& Fossey 1996, Sumsion & Smyth 2000, Wilkins et al 2001).
In addition to the use of the COPM with individual clients, the COPM
can also be used when occupational therapy intervention is provided for
a group or a community or organisation. For example, a group of clients
could have a shared occupational performance problem. As a result, this
group may be participating in a particular occupational therapy pro-
gramme. The COPM could be administered to individuals within the
group, but data analysed in aggregate form for use in programme evalu-
ation. If an organisation is the client, then the COPM interview still
focuses on occupational performance, but from the organisation’s per-
spective. The challenge in using the COPM in situations where the
organisation is the client is to identify the best individual(s) to respond
on behalf of the organisation. It is important that the COPM interview
focuses on the performance problems from the organisational perspective,
not from the perspective of a particular individual. In this way, the COPM
can be used to gain a unique perspective on performance issues that are
having an impact on the functioning of the organisation.
CASE EXAMPLES
The following case studies serve to illustrate the use of the COPM and
some of the challenges inherent in its use. The examples include an
individual respondent, multiple respondents, a group as respondent and
an organisation as respondent.
■ Leisure
– ‘I wanted to travel to Cuba this year, but I don’t have anyone to go
with. All my family members have passed on.’
– ‘I don’t write letters any more. I can’t hold a pen, or for that matter
an idea in my head.’
– ‘I used to be able to meditate, but can’t do that now.’
The issues Margaret identified on the COPM, which she thought were
important in order for her to be able to go home again, are shown in
Table 11.1.
The therapist worked with Margaret towards the most salient goal she
had set for herself – going home. A variety of housing options were
explored. In addition, the therapist focused on safety issues related to
using the walker, smoking and cooking meals, and facilitated some
increased insight into Margaret’s behaviour. After an agreed-upon period
of occupational therapy, a reassessment was completed. The results are
shown in Table 11.2.
CONCLUSION
Acknowledgements The authors wish to acknowledge the contributions of Mary Law, Sue
Baptiste and Hélène Polatajko, their co-authors of the Canadian Occu-
pational Performance Measure.
The Canadian Occupational Performance Measure 175
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Index
Moral dilemmas, 143 Outcome evaluation, 8, 68, 161–162 Personal development plans, 66
see also Ethical issues client-centred process, 27, 70 Person–Environment–Occupation
Multidisciplinary teams, 51, 61 physically disabled clients, 129, Clinical Model of Occupational
138–140, 142 Performance, 30
tools for, 138–140 Physical component, CMOP, 12–13
N see also Canadian Occupational Physical disabilities, clients with,
Performance Measure 123–144
Natural environment, 34–35 traditional approach, 23–24 barriers to client-centred care,
Networking, 67 Outcomes 125–126
Nick’s red wheelchair, 84–86 client-desired, 134–135, 138, 139, case examples, 140–142, 172–174
Norms, 32 140, 142–143 COPM, 172–174
measurement, 161–162 feeling valued, 131
see also Canadian Occupational goal setting, 128–130
O Performance Measure; having fun, 131
Outcome evaluation hopeful outcomes, 129–130
Obstacles to client-centred practice, shared vision, 128–130 interactive planning process,
46–51, 125–126 131–142
Occupation components, CMOP, assessment, 131–133, 137–138,
11–12 P 140, 141
Occupational deprivation, 114 case example, 140–142
Occupational therapy process Paediatric Activity Card Sort (PACS), challenging situations, 142–143
client-centred, 24–27, 68–70 151 client commitment, 138
mentally ill clients, 117 Paediatrics, client-centred practice in, client concerns/expectations,
traditional, 23–24 147–158 131–133, 140, 142–143
Older people, 91–103 assessments, 150–152 client-desired outcomes,
the ageing population, 91–92 case studies, 154–155, 156, 134–135, 138, 139, 140,
ageism, 98–99, 100, 102–103 171–172 142–143
attitudes of, 99–100 client insight, 157 client resources, 136–137, 141
attitudes to, 98–99, 102–103 COPM, 151, 156, 157, 168, clinician skills/knowledge,
building trust, 102 171–172 133–134, 140
co-morbidity, 96, 98 decision-making, 149, 155–156 evaluation, 138–140, 142
communication strategies, family involvement, 148–150, hypothesis generation, 135–
101–102 152–154, 155, 156, 157, 158 136, 141
COPM example, 170–171 identifying the client, 154–157, moral dilemmas, 143
decision-making, 100–101 158 plan development, 138,
degree of control, 100–101 implementation, 153–157, 158 141–142
environmental vulnerability, 97, 98 interventions, 150, 152–153 teamwork, 143
environments, 31–36, 50 key strategies, 153–154 treatment goal negotiation,
financial resources, 33–34, 92–94 literature on, 147–148 138, 142
frailty, 96–97, 98 school system, 157 validation of findings, 137–138,
gender distribution, 92, 93 system challenges, 153–154 141
health beliefs, 99 Pain, older people, 99, 100 reciprocity, 130, 141
health-related expenses, 94 Paperwork, 68 seven ingredients of care,
health status, 95–98 Partial client-centred practice, 16 123–124, 131
housing, 92, 93 Partnerships therapist–client synergy, 125–131
informal carers, 94 client-centred process, 26–27, 71 see also Paediatrics, client-centred
institutionalisation, 92, 93, older people, 99 practice in
99–100 in paediatrics, 157 Physical environments, 14, 35
life experiences, 100 power in, 43, 61–62 Pilot studies, 67
as pioneers, 92 therapist–client synergy, 125–131 Plan, Do, Study, Act (PDSA) cycle, 67
poverty, 93, 93 ‘Patient’, use of term, 39–40 Planning interventions, 69
rapport-building, 102 Patient-focused care, 57 COPM, 163, 164
sensory change, 95–96, 97, 98, Peer support, 65, 66, 67 Planning process, interactive see under
101–102 Perceived Efficacy and Goal Setting Physical disabilities, clients with
under-reporting of concerns, (PEGS), 151, 157 Political environments, 14, 33,
99–100, 102 Performance components, CMOP, 34
Organisations, COPM, 169–170, 12–14 Polypharmacy, older people, 96
173–174 Performance reviews, 66 Poverty, older people, 93, 93
INDEX 181
Power, therapist–client relationship, Royal Marsden Hospital model, 4 power, 41–44, 50, 60, 61–62
41–44, 50, 60, 61–62 Rural environments, 32–33 mentally ill clients, 117
mentally ill clients, 117 physically disabled clients, 125,
physically disabled clients, 125, 126, 130, 136
126, 130, 136 S reciprocity, 130, 141
reciprocity, 130, 141 synergistic, 125–131
Preferences for Activities of Children Safety, 46–47, 62–64, 143, 168 Tidal Model of client-centred practice,
(PAC), 152 Satisfaction, clients’, 113–114 3
Problem-solving process models, School-based practice, 157 Time factors, 50–51, 116–117
20–21 Self Instructional Programme COPM, 168–169
Problem-solving skills, clients’, 50, (COPM), 67, 68 Traditional therapy process, 23–24
152 Self-care, 11 Training see Education and training
Productivity, 12 mentally ill clients, 116 Traumatic brain injury, 76, 78
mentally ill clients, 115–116 Self-efficacy, 134–135 Treatment, clients’ ideas about, 132
Psychiatric rehabilitation see Mental Sensory change, older people, 95–96, Trust
illness, clients with 97, 98, 101–102 older people, 102
Punishment, illness as, 132 Sensory Profile, 152 physically disabled clients, 127,
Skills, therapists’, 66, 133–134, 140 134
Social environments, 14, 35–36
Q barriers to client-centred practice,
50 U
Qualitative research paradigm, Social roles, 36
110–111 Sociocultural component, CMOP, Under-reported problems, older
Quality of life, mentally ill clients, 116 12–13 people, 99–100, 102
Spirituality, CMOP, 12–14
Staff issues, 58–61
R education and training, 65–67, V
70–71
Rapport-building, 48 Standards, audits of, 68 Values
older people, 102 Stress, therapists’, 49 cognitively impaired clients, 81
physically disabled clients, 127 Supervision, 66 cultural, 32, 81
Reciprocity, synergistic relationships, Surrogate client-centredness, 83–84, older people, 100
130, 141 87 therapists’, 48
Red wheelchair example, 84–86 Synergistic relationships, 125–131 Videotaping, physically disabled
Reed and Sanderson model, 20 clients, 128–129
Referrals Visual aids, older people, 101,
client-centred process, 25, 69 T 102
traditional process, 23 Visual loss, older people, 96, 97
Reflective practice, 66 Teams
client-centred checklist, 70–71 audit of standards, 68
Rehabilitation, psychiatric see Mental education, 66, 70–71 W
illness, clients with multidisciplinary, 51, 61
Religion, spirituality and, 13 Teamwork, 59–60, 65–66, 67, 143 Work, mentally ill clients,
Resource files, 68 Therapist barriers to client-centred 115–116
Rights, clients’, 34 practice, 46–49, 125 Work environment, 50–51
Risks, client safety, 46–47, 62–64, Therapist–client relationship practice-related issues, 61–64,
143, 168 older people, 102 67–68
Role models, 58–59, 67 in paediatrics, 157 staff issues, 58–61, 70–71