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Research Review
Research Review
C. Ethical Principles
- The Belmont Report articulated three broad
principles on which standards of ethical conduct in
research are based: beneficence, respect for human
dignity, and justice.
Beneficence - imposes a duty on researchers
to minimize harm and maximize benefits.
Human research should be intended to produce
benefits for participants or—a situation that is
more common—for others.
1. The Right to Freedom from Harm and Discomfort -
Researchers have an obligation to avoid, prevent, or
minimize harm (nonmaleficence) in studies with
humans . Ethical researchers must use strategies to
minimize all types of harms and discomforts, even ones
that are temporary.
2. The Right to Protection from Exploitation - Involvement
in a study should not place participants at a
disadvantage or expose them to damages. Participants
need to be assured that their participation, or
information they might provide, will not be used
5. Ethical Guidelines in Research against them.
A. Codes of Ethics
- The Nuremberg Code : developed after Nazi atrocities Respect for Human Dignity
were made public in the Nuremberg trials, was an 1. The Right to Self-Determination - Humans should be
international effort to establish ethical standards. treated as autonomous agents, capable of controlling
- The Declaration of Helsinki, another international set their actions. Self-determination means that
of standards, was adopted in 1964 by the World prospective participants can voluntarily decide whether
Medical Association and was most recently revised in to take part in a study, without risk of prejudicial
2008. treatment. It also means that people have the right to
A.1. the American Nurses Association(ANA) issued ask questions, to refuse to give information, and to
Ethical Guidelines in the Conduct, Dissemination, and withdraw from the study.
implementation of Nursing Research (Silva, 1995). a. A person’s right to self-determination includes
The International Council of Nurses (ICN)updated in 2006 freedom from coercion, which involves
- ANA also published in 2001 a revised Code of Ethics for threats of penalty from failing to participate in
Nurses with Interpretive Statements, a document that a study or excessive rewards from agreeing
covers primarily ethical issues for practicing nurses but that to participate.
also includes principles that apply to nurse researchers.
- In Canada, the Canadian Nurses Association published a 2. The Right to Full Disclosure - People’s right to make
document entitled Ethical Research Guidelines for informed, voluntary decisions about study participation
Registered Nurses in 2002. requires full disclosure.
- Full disclosure means that the researcher has fully
described the nature of the study, the person’s right to
refuse participation, the researcher’s responsibilities, and the group not receiving the drug may be denied a
likely risks and benefits beneficial treatment.
a. covert data collection (concealment), which - Another dilemma can ariseif nurse researchers are
is the collection of data without participants’ confronted with conflict-of interest situations, in which
knowledge and consent. their expected behavior as researchers conflicts with
i. In some cases be acceptable if risks are their expected behavior as nurses (e.g., deviating from
negligible and participants’ right to a research protocol to give assistance to a patient).
privacy has not been violated.
ii. Covert data collection is least likely to be
ethically tolerable if the study is focused
on sensitive aspects of people’s behavior,
such as drug use or sexual conduct.
b. Deception which involves deliberately
withholding information about the study or
providing participants with false information.
Justice
1. The Right to Fair Treatment - Participant selection should
be based on study requirements and not on a group’s
vulnerability.
a. The principle of justice imposes particular
obligations toward individuals who are unable to
protect their own interests (e.g., dying patients)
to ensure that they are not exploited.
2. The Right to Privacy - Researchers should ensure that their
research is not more intrusive than it needs to be and that
participants’ privacy is maintained continuously.
Participants have the right to expect that their data will be
kept in strictest confidence.
a. Health Insurance Portability and Accountability Act
of 1996 (HIPAA), which articulates federal
standards to protect patients’ health information
b. the U.S. Department of Health and Human
Services issued the regulations Standards for
Privacy of Individually Identifiable Health
Information.
c. Most healthcare providers who transmit health
information electronically, compliance with these
regulations, known as the Privacy Rule, was
required as of April 14, 2003.
6. Research Misconduct
Research question: Are nurses equally empathy in their
treatment of male and female patients in the ICU?
Ethical dilemma: Ethics requires that participants be
aware of their role in a study. Yet if the researcher
informs nurse participants that their empathy in
treating male and female ICU patients will be
scrutinized, will their behavior be “normal?” If the
nurses’ usual behavior is altered because of the known
presence of research observers, then the findings will
be inaccurate.
Research question: What are the coping mechanisms
of parents whose children have a terminal illness?
Ethical dilemma: To answer this question, the
researcher may need to probe into the psychological
state of parents at a vulnerable time; such probing
could be painful or traumatic. Yet knowledge of the
parents’ coping mechanism might help to design
effective interventions for dealing with parents’ grief
and stress.
Research question: Does a new medication prolong life
in patients with cancer?
Ethical dilemma: The best way to test the effectiveness
of an intervention is to administer the intervention to
some participants but withhold it from others to see if
difference between the groups emerge. However, if the
intervention is untested (e.g., a new drug), the group
receiving the intervention may be exposed to
potentially hazardous side effects. On the other hand,
PRE-RECORDED OF SIR GAVIOL AND MDM TIONGCO ● Research can be undertaken in a NATURALISTIC or
RESEARCH REVIEW RELEVANT VIDEOS LABORATORY setting
● Research - is an inquiry that may be applied to all field of ○ Naturalistic setting is mostly applied in the
practice qualitative approach that the researcher allows the
- It is a systematic inquiry that uses disciplined phenomenon to happen in a natural setting,
method to answer questions and solve problems maybe in a community or in an organization, or
- With the disciplined method it may incorporate care facility
quantitative or qualitative approaches to be ○ Laboratory setting most of the researchers are
discussed later on experimental as it is controlled, it is concurrent
- Academe, evaluating research tool, developing with the design of the study being conducted
new methods for research
● Research data are pieces of information obtained in a study.
➔ SIR GAVIOLA EXPLANATION: ○ QUANTITATIVE data is numeric, it provides us
- When we move to the paradigm of nursing numbers and we are the ones who will interpret
research that is now the application of research those numbers
discipline principle strategy in the field of practice ○ QUALITATIVE data is narrative, wherein its an
of nursing focusing on researches that caters experience field narrative with an observation field
through the individual responses either the narrative, that's why the composition of the
individual, family, population and community in findings in qualitative researches are more on
general so we can have those areas of practice narrative, description, and interpretation about a
either quantitative or qualitative phenomena
● Nursing Research - is a systematic inquiry designed to ● Nurse researchers study about particular aspects of human
develop trustworthy evidence about issues of importance to behavior, characteristics or experience which are referred
the nursing profession, including nursing practice, to as:
education, administration and informatics. ○ CONCEPTS
○ CONSTRUCTS
IMPORTANCE OF NURSING RESEARCH ○ PHENOMENON
★ Research findings from rigorous studies provide strong ● Concepts in quantitative studies are referred to as
evidence for informing nurses’ decisions and actions VARIABLES.
➔ SIR GAVIOLA EXPLANATION: ○ Ex. studying on the attitude, willingness, the
- In your nursing informatics our accusation of knowledge, the compliance, the practice, self-
data information and knowledge leads to the determination, those may be aspects of study or
development of wisdom what you call variables
★ Research plays an important role in nursing terms of FUNDAMENTAL CONCEPTS AND TERMS
credentialing and status it helps the practice in nursing not - Variables should be conceptually and operationally defined to
only those who are doing researches but nurses in general be measurable.
to elevate their credential and profession to the ladder of
professionalism to achieve magnet status, administration A. Conceptual Definition- presents the theoretical meaning
needs to create, foster and sustain an environment where of concepts. Ex. pain
research is integrated in the delivery of nursing care.
➔ SIR GAVIOLA EXPLANATION: B. Operational Definition- presents the operations used to
- FYI, when you have come to hear that measure it.
principals have may be doctor of philosophy
of education or doctor of education, so there ex. Identify the conceptual and operational definition/s of
is a distinction there between the two anxiety.
professional achievements that they have
reached and it applies in the practice in ANXIETY
nursing as we have philosophy base, doctor 1. “...feelings of apprehension, tension, nervousness, and
degree and we also have the professional worry as measured by the State of Anxiety scale.
doctorate degree. Operational Definition: that is how the term anxiety is used
- In CDU, we have the philosophy base PHD in this particular study based on the state anxiety scale.
and that is your doctor of philosophy in 2. “..physiologic manifestations of uneasiness as measured by
nursing science and gears nurses of higher the palmar sweat index…”
professional credentials to engage in Operational Definition: Because it is being defined by the
developing knowledge tool.
3. “...a feeling of worry, nervousness, or unease, typically
Fundamental Concepts and Terms about an imminent event or something with an uncertain
outcome..”
● The RESEARCHER conducts the RESEARCH, while Defined because of the established theories and models of
INVESTIGATOR STUDY INVESTIGATION anxiety of the theorist.
● The STUDY PARTICIPANTS provides the data and they
may be called depending on the approach used in research: Classification of variable
○ SUBJECTS - for elemental
○ INFORMANT/KEY INFORMANT - for According to type of data:
qualitative researches 1. Categorical- categorizes the different data when it comes
○ RESPONDENTS - quantitative researches in from the qualitative
general 2. Discrete
○ POPULATION/SAMPLE 3. Continuous
According to degree of variability: ● Minimize bias, maximize precision and validity
1. Homogeneous
2. Heterogenous 4. EMPIRICAL
● Objectivity in data collection
According to relationship:
5. GENERALIZATION
● Relate research findings to the general population
According to relationship:
● That is why most quantitative researches requires
a huge number of samples coming from a
Associative Casual population group
5. QUALITATIVE DATA
QUANTITATIVE AND QUALITATIVE RESEARCH ● narrative , subjective
● Non-numeric (gender, beauty, etc.)
CHARACTERISTICS OF QUANTITATIVE RESEARCH
PHASES OF NURSING RESEARCH
1. DEDUCTIVE REASONING
● Develop specific predictions from general Phase 1: Conceptual Phase
principles 1. Formulation and delimiting the problem
2. Reviewing the related literature
2. SYSTEMATIC 3. Undertaking clinical fieldwork
● Logical series of steps according to plan of action ● To acquire experience of that particular subject
you are focusing
3. CONTROL 4. Defining the framework and definitions
5. Formulating hypothesis
● Some parts here don’t apply for qualitative research like - DOH embarked on Essential Newborn Care (program that
developing a hypothesis because you don’t don't addresses neonatal deaths in country).
hypothesize and you don't predict something to establish a - This program is an evidence-based strategic intervention
relationship or an effect because you are allowing the aimed at improving newborn care and helping cub neonatal
natural phenomena. mortality.
● If you do it in qualitative research, that may be a form of
bias that may affect the findings and analysis that you will Ethical Transgressions from the Past:
be making later on. - Nazi Medical Experiments (1933-1945)
- Tuskegee Syphilis Study (1932-1972)
Phase 2: Design and Planning Phase - Willowbrook Study (1960’s)
1. Selecting the research design - Jewish Chronic Disease Hospital Study (1960’s)
● What is the appropriate research design based on
how the variables are being measured and what CODE OF ETHICS
kind of output will you be looking for
2. Developing intervention protocols Code of Ethics are made to establish ethical standards and
3. Identifying the population prevent human rights violation
4. Designing the sampling plan
5. Specifying methods to measure variables The Belmont Report based on the US National Research Act
6. Procedures to safeguard participants in 1978, provided a model for many disciplinary guidelines
7. Finalizing the research plan - all of our ethics proceedings are based on this report
Phase 3: Empirical Phase The ICN Code of Ethics for Nurses was developed by the
1. Collecting the data International Council of Nurses (ICN)
2. Preparing the data for analysis
ICN CODE OF ETHICS FOR NURSES
Phase 4: Analytic Phase - An international code of ethics for nurses adopted by the
1. Analyzing the data International Council of Nurses in 1953
2. Interpreting the results - Latest review and revision completed in 2012
Phase 5: Dissemination Phase Principal Elements of the ICN Code of Ethics for Nurses
1. Communicating the findings
2. Utilizing the findings in Practice 1. Nurses and people
- These are the phases of qualitative research 2. Nurses and practice
- The planning phase of the study wherein we have to 3. Nurses and the profession
identify the research plot problem . If its phenomenology, 4. Nurses and co-workers
what is the phenomenon? To describe if its hemeneutics .
If its ethnography, what culture do we understand? - All of these covers ethical practices
- We develop a literature review and develop an overall
approach selecting and gaining entry into research sites by Government and Institutional Ethics Guidelines
establishing rapport and develop of safeguard to
participants. Philippine Health Research Ethics Board (PHREB)
- Next is to develop data collection strategies decides what - Created by the DOST (Department of Science and
type of data to gather and how to gather them. Technology) Special Order No. 091 of 2006
Verbalization=interview/ group discussion - Objective: ensure adherence to the universal principles for
- To decide from whom to collect the data = from entire the protection of human participants in research
population? Is it from specific population? And decide how
to enhance trustworthiness National Governance Structure for Ethics Review
- Gathering and analysis of data - organize, analyze and
evaluate data. Determine the saturation, and if u are not
satisfied with the saturation of the data
- Last phase will be disseminating of findings and conclusion
thus communicating the findings and utilizing findings in
practice and for future research
Informed Consent
- Ensure that participants know the full nature of the study
and are given the option to withdraw or participate
voluntarily
Components of Informed Consent: B. Respect for Human Dignity
1. Self-determination
1. Participant status - Voluntary participation
2. Study goals - Absence of coercion or threats
3. Type of data
4. Procedures 2. Full Disclosure
5. Nature of commitment - Describe the full nature of the study
6. Sponsorship
7. Participant selection C. Justice
8. Potential risks 1. Fair treatment
9. Potential benefits - Equal distribution of benefits and burdens
10. Alternatives - Honor all agreements made with participants
11. Compensation
12. Confidentiality pledge 2. Privacy
13. Voluntary consent - Keep data confidential
14. Right to withdraw and withhold information - Protect participants’ health information
15. Contact information
RESEARCH MISCONDUCTS
Sample: Informed Consent Form (Polit & Beck, 2012) “... fabrication, falsification or plagiarism in proposing,
performing, or reviewing research, or in reporting research
results...” U.S Public HEalth Service Regulation (2005)
Sample: Informed Consent Form (Burns & Grove, 2001) CDUCN CORE VALUES
● iNFORMED CONSENT
- Ensure that participants know the full nature of the study
and are given the option to withdraw or participate
voluntarily
- READ FURTHER DAW SA BOOK -.- (Tiongco, 2021)
● DATA SECURITY
- Anonymity
- Confidentiality
- Study participants have the right to expect that data they
provide will be kept in a strict confidence
- Participant’s right to privacy is protected through various
confidentiality procedures, we have:
Anonymity - should not be linked to participants
(can be done through assigning an identification
number to each participant and use it instead of
their names when they fill up the questionnaires )
Confidentiality - if there is a need or absence of
anonymity. When anonymity is impossible,
confidentiality procedures need to be implemented.
A promise of confidentiality is a pledge that any
information the participants will provide will not be
publicly reported in a manner that identifies them
and will not be accessible to others.
Research information should not be shared to
strangers nor with known people to the
participants.