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Exceptional Learners

Article in Oxford Review of Education · February 2020


DOI: 10.1093/acrefore/9780190264093.013.926

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Exceptional
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Exceptional Learners
Daniel P. Hallahan, Paige C. Pullen, James M. Kauffman, and Jeanmarie Badar
Subject: Cognition, Emotion, and Learning, Education, Health, and Social Services
Online Publication Date: Feb 2020 DOI: 10.1093/acrefore/9780190264093.013.926

Summary and Keywords

Exceptional learners is the term used in the United States to refer to students with dis-
abilities (as well as those who are gifted and talented). The majority of students with dis-
abilities have cognitive and/or behavioral disabilities, that is, specific learning disability
(SLD), intellectual disability (ID), emotional disturbance, (ED), attention deficit hyperac-
tivity disorder (ADHD), autism spectrum disorders (ASD). The remaining have primarily
sensory and/or physical disabilities (e.g., blindness, deafness, traumatic brain injury, cere-
bral palsy, muscular dystrophy).

Many of the key research and policy issues pertaining to exceptional learners involve
their definitions and identification. For example, prior to SLD being formally recognized
by the U.S. Department of Education in the 1970s, its prevalence was estimated at ap-
proximately 2% to 3% of the school-age population. However, the prevalence of students
identified for special education as SLD grew rapidly until by 1999 it reached 5.68% for
ages 6 to 17 years. Since then, the numbers identified as SLD has declined slowly but
steadily. One probable explanation for the decrease is that response to intervention has
largely replaced IQ-achievement as the method of choice for identifying SLD.

The term intellectual disability has largely replaced the classification of mental retarda-
tion. This change originated in the early 2000s because of the unfortunate growing popu-
larity of using retard as a pejorative. Although ID used to be determined by a low IQ-test
score, one must also have low adaptive behavior (such as daily living skills) to be diag-
nosed as ID. That is the likely reason why the prevalence of students with ID at under 1%
is well below the estimated prevalence of 2.27% based solely on IQ scores two standard
deviations (i.e., 70) below the norm of 100.

There are two behavioral dimensions of ED: externalizing (including conduct disorder)
and internalizing (anxiety and withdrawal) behaviors. Research evidence indicates that
students with ED are underserved in public schools.

Researchers have now confirmed ADHD as a bona fide neurologically based disability.
The American Psychiatric Association recognizes three types of ADHD: (a) ADHD, Pre-
dominantly Inattentive Type; (b) ADHD, Predominantly Hyperactive-Impulsive Type; and
(c) ADHD, Combined Type.

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The American Psychiatric Association recognizes two types of ASD: social communication
impairment and repetitive/restricted behaviors. The prevalence of ASD diagnosis has in-
creased dramatically. Researchers point to three probable reasons for this increase: a
greater awareness of ASD by the public and professionals; a more liberal set of criteria
for diagnosing ASD, especially as it pertains to those who are higher functioning; and “di­
agnostic substitution”—persons being identified as having ASD who previously would
have been diagnosed as mentally retarded or intellectually disabled.

Instruction for exceptional children, referred to as “special education,” differs from what
most (typical or average) children require. Research indicates that effective instruction
for students with disabilities is individualized, explicit, systematic, and intensive. It differs
with respect to size of group taught and amount of corrective feedback and reinforce-
ment used. Also, from the student’s viewpoint, it is more predictable. In addition, each of
these elements is on a continuum.

Keywords: exceptional children, special education, Individuals with Disabilities Education Act, learning
disabilities, intellectual disabilities, emotional disturbance, attention deficit hyperactivity disorder,
autism, re- sponse to intervention, evidence-based instruction

Introduction
This article addresses fundamental information and issues pertaining to exceptional
learners and their education. Although the term exceptional learners sometimes includes
those who are gifted or talented, this article concentrates on those with disabilities. More
specifically, the focus is on students with cognitive and behavioral disabilities, who com-
prise approximately 70% of students identified with disabilities, with the remaining iden-
tified with several different sensory and physical impairments (e.g., blindness, deafness,
traumatic brain injury, cerebral palsy, muscular dystrophy, and so forth; U.S. Department
of Education, 2018). In addition, the article focuses on exceptional learners in the United
States although much of what is covered is applicable to other countries. (For information
on the identification and education of exceptional learners in other countries, see, e.g.,
Anastasiou & Keller, 2017; Artiles & Hallahan, 1995; Wehmeyer & Patton, 2017).

Definition of Exceptional Learners


In the context of education, exceptional learners “differ from most . . . individuals in a
particular way that is relevant to their education. Their particular educationally relevant
difference demands instruction that differs from what most (typical or average) learners
require” (Hallahan, Kauffman, & Pullen, 2019, p. 6). The use of the term “exceptional”
originated in the latter part of the 20th century as a euphemism to replace denoting stu-
dents with disabilities as “handicapped.” The particular disabilities, as recognized by the
U.S. Department of Education, are specific learning disability, speech or language im-
paired, other health impairment, autism, intellectual disability, emotional disturbance, de-
velopmental delay, multiple disabilities, hearing impairment, orthopedic impairment, visu-

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al impairment, traumatic brain injury, and deaf-blindness (U.S. Department of Education,
2018).

Prevalence of Exceptional Learners


Many key issues pertaining to exceptional learners are encapsulated in the rates at which
U.S. public schools identify students with disabilities in each of the categories of special
education. When Public Law 94-142 (now the Individuals with Disabilities Education Im-
provement Act [IDEA]) was passed into law in 1975, it mandated that an annual report be
made to Congress that, among other things, would include the number of students served
by special education in each of the disability categories. Thus the topic of prevalence has
been at the core of many important issues concerning exceptional learners, which is un-
derstandable because it reflects how disabilities are defined and students with disabilities
are identified.

Debates over definition of exceptional learners proliferate, even with respect to those
that would seemingly be easily delineated, such as blindness and deafness (Hallahan et
al., 2019). However, disability categories garnering the most attention with respect to def-
inition and identification are the higher prevalence disabilities, such as specific learning
disabilities (SLD); intellectual disabilities (ID); emotional disturbance (ED); attention
deficit hyperactivity disorder (ADHD), which accounts for a large percentage of students
identified as having other health impairment (OHI); and autism, or autism spectrum dis-
orders (ASD).

Figures 1 and 2 depict prevalence rates over time for SLD, ID, ED, OHI, and autism for
students 6 to 17 and 6 to 21 years of age, respectively. Beginning in 2006, annual reports
to Congress have only reported prevalence rates for 6 to 21 years of age. Prevalence
rates in Figure 2, as expected, are lower than Figure 1 because few general education
students stay in school past age 17 and not all students with disabilities remain in school
to the age of 21 years.

The rest of this article is composed of three parts. The first part introduces the aforemen-
tioned types of exceptional learners and issues associated with each, concentrating main-
ly on definitions and prevalence rates. The second part discusses instruction for excep-
tional learners. Finally, we draw general conclusions focusing on issues pertaining to the
educational placement of exceptional learners in special and general education.

Specific Learning Disabilities


SLD was largely born out of parents’ frustrations with schools not providing needed ser-
vices for their children (Hallahan & Mercer, 2002; Kirk, 1962, 1963). Their children were
struggling academically, but they had IQ scores too high to qualify as “mentally
retarded” (now referred to as “intellectually disabled”). Largely propelled by parent pres-

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sure, the federal government officially recognized SLD as a special education category in
1975 with passage of Public Law 94-172.

Defining Specific Learning Disabilities

The most commonly accepted definition of SLD, and the one primarily used by schools in
the United States, is the one first introduced in Public Law 94-142 and, with minor adjust-
ments, included in the 1997 and 2004 IDEA reauthorizations:

GENERAL—The term “specific learning disability” means a disorder in one or


more of the basic psychological processes involved in understanding or in using
language, spoken or written, which disorder may manifest itself in an imperfect
ability to listen, think, speak, read, write, spell, or do mathematical calculations.

DISORDERS INCLUDED—Such term includes such conditions as perceptual dis-


abilities, brain injury, minimal brain dysfunction, dyslexia, and developmental
aphasia.

DISORDERS NOT INCLUDED—Such term does not include a learning problem


that is primarily the result of visual, hearing, or motor disabilities, of mental retar-
dation, of emotional disturbance, or of environmental, cultural, or economic disad-
vantage (IDEA, Amendments of 1997, Sec. 602(26), p. 13).

Prevalence of Specific Learning Disabilities

SLD has for some time accounted for the greatest percentage of students identified for
special education. As SLD was being proposed as a category of special education, it was
estimated that its prevalence would be about 2% to 3% of the school-age population.
Once states began reporting, per federal requirements, actual numbers of students iden-
tified and served, however, it became obvious that this was an underestimate. As Figure 1
shows, SLD increased steadily, more than doubling by 1999 when it reached its asymp-
tote of 5.68% for students 6 to 17 years.

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Figure 1. Prevalence rates for SLD, MR, EBD, OHI,


and autism, 1995–2005.

The rapid expansion of SLD spawned a number of critics over the years who have dispar-
aged the SLD category. Criticism has been generally of two types, those expressing
doubts concerning (a) the validity of the SLD category (i.e., whether it is “real”) and (b)
the methods for determining whether a student has SLD.

Criticism of SLD: Questionable Validity as a Disability


From its inception, there have been those who have cast doubt on the very existence of
SLD. One of the earliest criticisms asserted that SLD was a convenient way for schools
and parents to explain the failures of children from White, middle class families to meet
the academic standards that were being ratcheted up by a society bent on competing
globally via economic and military progress (Sleeter, 1987). At the same time, SLD was al-
so branded by some as a socially constructed phenomenon fitting a sociological model
based on an ideology of race- and class-based oppression of minorities.

Although viewing SLD as emerging from an ideology of oppression was an extreme cri-
tique, it was consonant with more mainstream criticisms that focused on questionable
claims regarding its etiology. SLD was built largely on the assumption that it was caused
by what was referred to as minimal brain dysfunction (Clements, 1966). Given the rela-
tively crude state of neurological diagnosis in the latter part of the 20th century, claims of
neurological involvement at the time were speculative.

With the advent of neuroimaging technology in the 1990s, however, evidence emerged
supporting neurological dysfunction as a cause of SLD (Flowers, 1993; Flowers, Wood, &
Naylor, 1991; Gross-Glenn et al., 1991; Hagman et al., 1992; Hynd & Semrud-Clikeman,
1989; Kushch et al., 1993; Larsen, Hoien, Lundberg, & Odegaard, 1990; Shaywitz et al.,
1998). Today, substantial evidence has accumulated supporting neurological dysfunction
as a cause of many instances of SLD (Gabrieli, 2009; Hoeft et al., 2011; Peterson & Pen-
nington, 2015; Saygin et al., 2013). Furthermore, evidence strongly supports a hereditary
basis in many cases (DeFries, Gillis, & Wadsworth, 1993; DeThorne et al., 2006; Lewis &

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Thompson, 1992; Reynolds et al., 1996; Shalev, 2004). Establishing a biological basis of
SLD thus blunted much of the criticism challenging the validity of SLD as a legitimate dis-
ability.

Criticism of SLD: Identification Methods


With the designation of SLD as a category of special education in the 1970s, the federal
government also published regulations regarding SLD determination. In order to be said
to have SLD, the student was to exhibit a severe discrepancy between achievement and
intellectual ability. Most state departments of education relied on an IQ-achievement dis-
crepancy, with some using statistical formulas, to identify students with SLD. Over the
years, statisticians have determined these formulas to be less than perfect. In addition, an
IQ-achievement approach is problematic in the earliest grades because very little reading
or math skills are expected of students at this point, which has led to this method being
referred to as a “wait-to-fail” model. Such problems have led influential researchers to
declare an IQ-achievement approach as invalid, inappropriate, or unnecessary (e.g.,
Fletcher et al., 2002; Gresham, 2002; Siegel, 1989).

Response to Intervention

In answer to the criticism of IQ-achievement discrepancy, an alternative method of identi-


fying students with SLD has been proposed: response to intervention (RtI). Although by
law RtI is not mandated and IQ-achievement is still permissible, the U.S. Department of
Education encourages states to use RtI. RtI refers to a student’s change (or lack of
change) in academic performance or behavior as a result of instructional intervention
(Duhon, Messmer, Atkins, Greguson, & Olinger, 2009; Fuchs, Mock, Morgan, & Young,
2003; O’Connor, Sanchez, & Kim, 2017). Implementation of RtI is highly variable from
school district to school district, but the path to identification of a student as having SLD
typically involves some variation of the following. The student (a) receives quality instruc-
tion in the general education classroom and does not do as well as peers, (b) receives in-
tervention in the form of small group instruction and still does poorly, (c) is referred for
formal evaluation for special education, and (d) is determined by an interdisciplinary
team to have SLD, which results in the development of an individualized education pro-
gram.

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Figure 2. 6 to 21 years of age: Prevalence figures for


SLD, ID, BD, OHI, and autism, 1995–2015.

RtI is rapidly replacing IQ-achievement discrepancy as a means of identifying students


with SLD. However, researchers have presented several criticisms of RtI (O’Connor et al.,
2017; Pullen & Hallahan, 2015; Pullen, Lane, Ashworth, & Lovelace, 2017; Vaughn &
Fuchs, 2003; Yell, 2019). Most of these criticisms have focused on, or been related to, the
inconsistency with which RtI has been interpreted and implemented (Hudson & McKen-
zie, 2016). For example, considerable variability exists with respect to such things as type
of instruction, duration of instruction, and who the instructor is (e.g., general education
teacher, special education teacher, school psychologist, paraprofessional). Such variabili-
ty is undoubtedly a factor in the paucity of evidence on the effectiveness of RtI when im-
plemented at scale. Correlated with, and perhaps affected by, the growing popularity of
RtI, the rising prevalence of SLD slowed and reversed course in the first decade of the
21st century. As shown in Figures 1 and 2, after SLD’s asymptote of 5.68% in 1999, it has
declined slowly but steadily (Pullen, 2017).

Intellectual Disabilities
At one time, people with intellectual disabilities were referred to as mentally retarded.
However, by the early 2000s, the pejorative retard had regrettably reached such a level of
use that professionals, family members, and persons with intellectual disabilities them-
selves expressed discomfort with the term mental retardation. Unfortunately, throughout
history, people with subaverage intellectual abilities have been ridiculed. In fact, as late
as the early 1900s the terms idiot, imbecile, and moron were used by professionals and
professional organizations to refer to individuals with severe, moderate, or mild intellec-
tual disability or mental retardation, respectively. In 2007, the major professional organi-
zation for people with significant cognitive or intellectual disabilities—the American Asso-
ciation on Mental Retardation (AAMR)—changed its name to the American Association on
Intellectual and Developmental Disabilities. Furthermore, in 2010, Public Law 111-256
mandated that intellectual disability replace mental retardation in many areas of the fed-
eral government. As of 2016, the term mental retardation was only being used in the
State Department of Education in three states (Polloway, Bouck, Patton, & Lubin, 2017).

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Defining Intellectual Disabilities

ID is currently defined by the American Association on Intellectual and Developmental


Disabilities as follows: “a disability characterized by significant limitations both in intel-
lectual functioning and in adaptive behavior as expressed in conceptual, social, and prac-
tical adaptive skills. This disability originates before age 18” (AAMR Ad Hoc Committee
on Terminology and Classification, 2010, p. 1).

At one time, mental retardation (now ID) was determined by an IQ test, with a score of 70
or below indicative of probable mental retardation. In addition to the terminology change
from mental retardation to intellectual disabilities, a significant difference in definition
from several years ago has been the recognition of adaptive behavior as a critical compo-
nent of determining ID.

Prevalence of Intellectual Disabilities

Figures 1 and 2 indicate that the prevalence of students identified as ID for special educa-
tion is lower than one would expect based on other factors. For example, theoretically, we
expect 2.27% of the population to fall two standard deviations (IQ = 70 on the Wechsler
Intelligence Scale for Children, Fourth Edition) or more below this average. This expecta-
tion is based on the assumption that intelligence, like so many other human traits, is dis-
tributed along a normal curve. Researchers have pointed to three likely reasons for the
discrepancy: (a) use of adaptive behavior in addition to an IQ score to diagnose ID, (b)
preference to label students with IQs in the 70s as learning disabled because it is less
stigmatizing (MacMillan, Gresham, Bocian, & Lambros, 1998), and/or (c) preference for
identifying children as having ASD because of increased awareness of this condition.

Emotional Disturbance
Generally, researchers recognize two behavioral dimensions of ED: externalizing behavior
(including conduct disorder) and internalizing (anxiety and withdrawal). The former in-
volves striking out against others (Furlong, Morrison, & Jimerson, 2004; Kazdin, 1995)
whereas the latter involves mental or emotional conflicts, such as depression and anxiety
(Gresham & Kern, 2004). Although not mutually exclusive, research indicates poorer out-
comes for students with externalizing behavior disorders (Kauffman & Landrum, 2018).
Research indicates that boys outnumber girls with respect to externalizing disorders,
with the opposite true for internalizing disorders, although some girls exhibit externaliz-
ing and such disorders in girls appear to be increasing (Javdani, Sadeh, & Veerona, 2011).
In addition, students with externalizing disorders, undoubtedly because of their overt be-
haviors, are much more likely than those with internalizing disorders to be identified as
ED for special education services (Kauffman & Landrum, 2018).

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Defining Emotional Disturbance

Most school divisions use the federal definition of ED or some variation:

i. The term means a condition exhibiting one or more of the following characteristics
over a long period of time and to a marked extent, which adversely affects education-
al performance:
A. An inability to learn that cannot be explained by intellectual, sensory, or
health factors;
B. An inability to build or maintain satisfactory relationships with peers and
teachers;
C. Inappropriate types of behavior or feelings under normal circumstances;
D. A general pervasive mood of unhappiness or depression; or
E. A tendency to develop physical symptoms or fears associated with personal or
school problems.

ii The term includes children who are schizophrenic. The term does not include chil-
dren who are socially maladjusted unless it is determined that they are emotionally
disturbed. (45 C.F.R. 121a5[b][8][1978])

Notably, IDEA provides no guidance on distinguishing maladjustment from ED, which has
resulted in many researchers claiming the futility of trying to separate social maladjust-
ment from ED. It was Eli Bower who first suggested the definition in the 1950s without
the exclusion of social maladjustment (Bower, 1982; Kauffman & Landrum, 2018). A more
reasonable definition has been suggested by Forness and Knitzer (1992), but it has not
been adopted in federal law. As testament to the complexity of differentiating social mal-
adjustment from ED, a review of case law found judges applying a variety of principles in
interpreting facts, resulting in rulings showing little conformity (Sullivan & Sadeh, 2014).

Prevalence of Emotional Disturbance

Figures 1 and 2 reveal that fewer than 1% of students have been consistently identified
for special education as ED. This low prevalence rate, however, flies in the face of find-
ings by several other researchers who have uncovered higher rates, ranging from 6% to
10% (Forness, Freeman, Paparella, Kauffman, & Walker, 2012; Kauffman & Landrum,
2018; Kauffman, Mock, & Simpson, 2007; Landrum, 2017). The U.S. Surgeon General’s
report at the turn of the century (U.S. Public Health Service, 2000) and a report by the
Centers for Disease Control and Prevention (CDC, 2013) have documented that only a
very small percentage of children with ED receive mental health services. Furthermore,
data from the National Survey of Children’s Health (Child and Adolescent Health Mea-
surement Initiative, 2012) reveal that parents report having been informed by a profes-
sional that their child has mental health problems at a substantially higher rate than the
number of students being served as ED in schools. In addition, NSCH data reveal that be-
tween the years of 2003 to 2011, children with internalizing behaviors, specifically anxi-
ety and depression, increased; longitudinal data indicate that children being served in

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schools as ED decreased slightly during that same time period (Pullen, Ryoo, & Hallahan,
2019).

Attention Deficit Hyperactivity Disorder


Although sometimes considered a bogus, “fad” diagnosis, persons who today would be
very likely considered ADHD were recognized in the medical literature as far back as the
18th century. Dr. Melchior Weikard, a highly respected German physician, serving in pres-
tigious government positions (e.g., court physician to an empress, a prince-bishop, and a
tsar) is recognized as the first to write about ADHD-like symptoms (Barkley & Peters,
2012). In 1775, Weikard wrote, “Lack of Attention,” a chapter in which he described the
inattentive person as having deficits in concentration and being distracted by “every
humming fly, every shadow, every sound, the memory of old stories [drawing] him off task
to other imaginations . . . [hearing] only half of everything” (Barkley & Peters, 2012, p. 5).
Not long after Weikard’s publication, Sir Alexander Chrichton (1798) theorized that a per-
son could be born with attention disorders or could acquire them through diseases affect-
ing the brain.

Defining ADHD

IDEA does not recognize ADHD as separate category of special education. In the 1980s,
professionals and parents advocated for ADHD. ADHD advocates claimed that the federal
government made this decision partially based on the fear that including ADHD would
lead to a substantial increase in the numbers of students qualifying for special education
services. In any case, as part of the answer to advocates’ concerns, the U.S. Department
of Education decided to include ADHD within the category of OHI. IDEA defines OHI as
follows:

having limited strength, vitality, or alertness, including a heightened alertness to


environmental stimuli, that results in limited alertness with respect to the educa-
tional environment, that—

(i) Is due to chronic or acute health problems such as asthma, attention


deficit disorder or attention deficit hyperactivity disorder, diabetes, epilepsy,
a heart condition, hemophilia, lead poisoning, leukemia, nephritis, rheumatic
fever, sickle cell anemia, and Tourette syndrome; and
(ii) Adversely affects a child’s educational performance. (§300.8[c][9]; italics
added).

The American Psychiatric Association (2013) recognizes three subtypes of ADHD: (a) AD-
HD, Predominantly Inattentive Type; (b) ADHD, Predominantly Hyperactive-Impulsive
Type; and (c) ADHD, Combined Type. Examples of criteria used to determine these sub-
types include (a) for inattention: difficulty sustaining attention, distractible; (b) for hyper-

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activity: fidgeting, leaving seat at inappropriate times, talking excessively; (c) for impul-
sivity: problems awaiting one’s turn, interrupting others.

Prevalence of ADHD

Advocates have claimed that the federal government was afraid that including ADHD as a
specific category in IDEA would further expand a growing population of students identi-
fied for special education, who would thus be guaranteed services. Evidence of the
government’s concern is contained in a U.S. Department of Education’s Memorandum in
1991, which states “While estimates of the prevalence of ADD vary widely, we believe
that three to five percent of school-aged children may have significant educational prob-
lems related to this disorder” (Joint Policy Memorandum [ADD] Office of Special Educa-
tion and Rehabilitative Services, September 16, 1991).

Given that only about 1% of students are identified as OHI (see Figures 1 and 2), it is like-
ly that students with ADHD are underidentified for special education. At the same time,
these figures reveal that the prevalence of students categorized as OHI has increased
dramatically, rising over 400% from 1995 to 2015. In addition, research suggests that
some students receiving services as emotionally disturbed or learning disabled are also
ADHD (Schnoes, Reid, Wagner, & Marder, 2006). Some critics have asserted that this in-
crease is artificial, due to U.S. society’s emphasis on achievement and conformity. Howev-
er, prevalence of ADHD globally, such as in Africa, the Middle East, Oceania, South Amer-
ica, Asia, North America, and Europe, have indicated a worldwide prevalence of 3.4% to
5.29% (Polanczyk, Salum, Sugaya, & Rohde, 2015; Polanczyk, Silva de Lima, Horta, Bie-
derman, & Rohde, 2007).

Autism
Although we can trace recognition of autism in the psychiatric literature back to the
1940s (Asperger, 1944/1991; Kanner, 1943/1973), it has only been a separate category
under the IDEA since 1990. Most researchers now refer to it as ASD to emphasize that
the disabilities associated with ASD fall on a continuum from relatively mild to severe.
For example, the American Psychiatric Association’s (2013) Diagnostic and Statistical
Manual of Mental Disorders (fifth edition; DSM-5) uses the term “autism spectrum disor-
ders” as an umbrella term.

Defining Autism Spectrum Disorders

The symptoms of ASD vary considerably, but the DSM-5 classifies them as consisting of
two general types: “social communication impairment” and “repetitive/restricted behav-
iors.” Asperger syndrome, a term which is often used in practice, is no longer recognized
in the DSM-5 as a separate entity; instead, a person whose intellectual and verbal abili-
ties are relatively high is considered to be a person with ASD who is high functioning in
some areas. Specifically, the DSM-5 criteria are

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Persistent deficits in social communication and social interaction across multiple
contexts, as manifested by the following, currently or by history (examples are il-
lustrative, not exhaustive):

1. Deficits in social-emotional reciprocity, ranging, for example, from abnor-


mal social approach and failure of normal back-and-forth conversation; to re-
duced sharing of interests, emotions, or affect; to failure to initiate or re-
spond to social interactions.
2. Deficits in nonverbal communicative behaviors used for social interaction,
ranging, for example, from poorly integrated verbal and nonverbal communi-
cation; to abnormalities in eye contact and body language or deficits in under-
standing and use of gestures; to a total lack of facial expressions and nonver-
bal communication.
3. Deficits in developing, maintaining, and understand relationships, ranging,
for example, from difficulties adjusting behavior to suit various social con-
texts; to difficulties in sharing imaginative play or in making friends; to ab-
sence of interest in peers.

Prevalence of Autism Spectrum Disorders

When the U.S. Department of Education first recognized autism in the early 1990s as a
category of special education, the percentage identified for services was minimal (see
Figures 1 and 2). Immediately, however, the prevalence jumped substantially (e.g., by
about 600% from 1995 to 2005 for students 6 to 17 years old). Since then, the figures
have increased steadily and significantly. For example, for students 6 to 21 years old, the
prevalence has increased from 0.54 in 2005 to 0.80 in 2015.

The CDC’s Autism and Developmental Disabilities Monitoring Network has been monitor-
ing the prevalence of ASD since the early 2000s. As of 2018, the CDC reported that 1 in
59 persons (1.69%) under 21 years of age was diagnosed with ASD (Baio et al., 2018).
Like the U.S. Department of Education, the CDC has documented a substantial increase
in ASD over time. Figure 3 reveals a growth of almost 300% between 2000 and 2014. It is
important to point out that the prevalence figures reported by the CDC are well above
those reported by the U.S. Department of Education.

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Figure 3. Prevalence rates of autism, 2000–2014


(Centers for Disease Control and Prevention).

Researchers have generally attributed the increased prevalence of ASD (Fombonne, 2001;
Frith, 2003; Matson & Kozlowski, 2011; National Research Council, 2001; Shattuck, 2006;
Van Naarden Braun et al., 2015; Wing & Potter, 2002) to three factors, most likely in com-
bination: (a) a greater awareness of ASD by the public and professionals; (b) a more liber-
al set of criteria for diagnosing ASD, especially as it pertains to those who are higher
functioning; and (c) “diagnostic substitution,” referring to the phenomenon of persons
now being identified as having ASD who previously would have been diagnosed as men-
tally retarded or intellectually disabled. For example, as shown in Figure 1, for students 6
to 17 years of age, the percentage of students identified as autistic grew from 0.06% to
0.37% from 1995 to 2005 whereas during this same period of time students identified as
ID decreased from 1.13% to 0.94%. And, as Figure 2 reveals, for students 6 to 21 years of
age, students identified as autistic rose from 0.05% to 0.80% from 1995 to 2015 whereas
ID dropped from 0.96% to 0.60%.

It is well established the cause of ASD is neurologically based (National Institute of


Health, 2013), with strong evidence that genetic factors are at play (Stichter, Conroy,
O’Donnell, & Reichow, 2017). However, the exact interplay of these factors is a puzzle far
from being solved. Just a few clues researchers are investigating are (a) “neuronal under-
connectivity”—a disruption of cells communicating with each other from different areas
of the brain (Elison et al., 2013; Just, Keller, Malave, Kana, & Varma, 2012; (b) microbio-
me dysregulation—evidenced by immune and gastrointestinal issues (Vuong & Hsiao,
2017); (c) environmental toxins, such as lead and mercury (Hertz-Picciotto & Delwiche,
2009; Volk, Lurmann, Penfold, Hertz-Picciotto, & McConnell, 2013); and (d) genetic muta-
tions—sometimes passed down to children from one or both parents (Autism Genome
Project Consortium, 2007; Sebat et al., 2007).

With respect to toxins, one particularly controversial and unproven theory is that the
measles, mumps, rubella (MMR) vaccine can cause ASD. The presumption that vaccines
cause ASD owes its origin to an article published in the prestigious journal The Lancet
(Wakefield et al., 1998). The notion of such a link caught on quickly, largely reinforced by
the fact that some of the first signs of ASD occur about the same time as when the vac-
cine is administered. Wakefield’s research received harsh criticism from the scientific

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community, with several of the study’s authors registering retractions, The Lancet
recording a retraction of the article, and Wakefield eventually being stricken from the
U.K. Medical Register for unethical behavior (Meikle & Boseley, 2010).

Numerous governmental and independent critiques of the MMR vaccine theory have de-
termined it is baseless (Institute of Medicine, 2004; Taylor, Swerdfeger, & Eslick, 2014).
However, believers in its findings continue to trigger intermittent outbreaks of measles
(Healio, 2018), putting the public at risk for outbreaks of measles, which can lead to
pneumonia and death and, if contracted in pregnancy, severe developmental disabilities
and blindness in newborns.

Instruction for Exceptional Learners


Instruction for exceptional children, referred to as “special education,” differs from what
most (typical or average) children require (Hallahan et al., 2019; Kauffman & Konold,
2007; Stichter et al., 2008). The U.S. Department of Education defines special education
as

specially designed instruction, at no cost to the parents, to meet the unique needs
of a child with a disability, including

(i) Instruction conducted in the classroom, in the home, in hospitals and insti-
tutions, and in other settings; and
(ii) Instruction in physical education. (IDEA 34 CFR §300.39)

As a practical matter, special education differs from general education in several ways.
Special education is more individualized, explicit, systematic, and intensive. It differs with
respect to size of group taught and amount of corrective feedback and reinforcement
used (Pullen & Hallahan, 2015). Also, from the student’s viewpoint, it is more predictable.

Individualized

Individualized instruction is fundamental to special education. General education teach-


ers, because of the range of students’ abilities in their classrooms, aim instruction to
meet the needs of the maximal number of students, those in the middle range of abilities
(Gerber & Semmel, 1984). Special education teachers, on the other hand, are prepared to
focus on individual students and each student’s instructional needs.

Special education’s individualized instruction is reified by law. Fred Weintraub, an instru-


mental architect of Public Law 94-142, asserted:

The cornerstone of special education policy for the past four decades has been in-
dividualization. IDEA was and remains unique in educational policy in that it pre-
scribes no truth in what is appropriate for children with disabilities. Rather, it pro-

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vides for a process whereby the individualized educational program (IEP) team
that knows the child determines what is appropriate for the child.

(Weintraub, 2012, p. 53)

Explicit

Pullen and Hallahan (2015) offer the definition of explicit from the CO-BUILD Advanced
Dictionary of American English (Harper Collins, 2012), “something that is explicit is ex-
pressed or shown clearly and openly, without any attempt to hide anything.” Further, it in-
volves the teacher explaining “skills and concepts in a clear and direct manner. If instruc-
tion is explicit, the teacher provides a clear explanation or model of the skill or
concept” (Pullen & Hallahan, 2015, p. 38). In their book Explicit Instruction: Effective and
Efficient Teaching, Archer and Hughes (2011) propose a very similar definition:

[It] is called explicit because it is an unambiguous and direct approach to teaching


that . . . is characterized by a series of supports or scaffolds, whereby students are
guided through the learning process with clear statements about the purpose and
rationale for learning the new skill, clear explanations and demonstrations of the
instructional target, and supported practice with feedback until independent mas-
tery has been achieved. (p. 1)

Systematic

Something done systematically is done according to an organized plan; for example, a


occurs first, b occurs second, c occurs third, and so on. With respect to special education
students, systematic instruction usually means teaching easier before more difficult skills
and teaching pre-skill strategies before teaching the strategy. It also requires students to
repeat skills or skill sequences until ready to move on to more difficult skills (Carnine, Sil-
bert, Kame’enui, Tarver, & Jungjohann, 2006). This emphasis on repetition is designed to
promote automaticity to counter the halting pattern of skill acquisition so often present in
students with disabilities.

Intensive

Something done intensively maximizes the ratio between the effort and the time it takes
to do something (Harper Collins, 2012). Because students identified for special education
services are behind other students academically, intensive instruction helps them
progress as quickly as possible. Intensity of instruction is influenced by the size of the
group instructed and by duration and frequency of instruction (Pullen & Hallahan, 2015).

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Instructional Group Size

Research indicates that the smaller the group instructed, the more effective the instruc-
tion. Not surprisingly, one-on-one instruction is the most effective, followed by small-
group instruction and whole-class instruction (Wanzek & Kent, 2012). In practice, with re-
spect to classroom instruction, one-on-one instruction is rarely possible. Small-group in-
struction is possible especially in the context of RtI or tiered instruction. What little re-
search exists suggests that the best size of small groups is three to five (Gersten et al.,
2009; Rashotte, MacPhee, & Torgesen, 2001).

Frequency and Duration of Instruction

Frequency is usually defined as the number of times an event occurs over a specified peri-
od of time. Duration usually refers to the length of time something continues. In practice,
with respect to classroom instruction, students with disabilities may require more fre-
quent interventions each day and/or week, and they may need to continue this schedule
of instruction for a relatively extended period of time (e.g., one semester, one year, or per-
haps even over multiple years; Vaughn et al., 2010).

Corrective Feedback

Abundant research supports the use of corrective feedback for students with learning dis-
abilities (Brosvic, Dihoff, Epstein, & Cook, 2006; Chard, Vaughn, & Tyler, 2012; Eckert,
Dunn, & Ardoin, 2006; Heubusch & Lloyd, 1998; Kouri, Selle, & Riley, 2006; Wanzek et
al., 2006). The beneficial effects apply to several academic areas, including reading word
recognition, comprehension, and fluency; spelling; and acquisition of math facts. The
more immediate and explicit the correction, the more likely it will have a beneficial effect
(Pullen & Hallahan, 2015). Being explicit helps to ensure that the student understands
why his or her response was incorrect, as well as to understand and be able to generate
the correct response. In order to help the student to understand why the response was in-
correct, it is often helpful for the teacher to model the correct response.

Reinforcement

Reinforcement of correct academic responding or appropriate behavior is the sine qua


non of a behavioral approach to instruction. Decades of research document the effective-
ness of using behavioral principles in teaching students with disabilities (Cooper, Heron,
& Heward, 2019). These behavioral teaching methodologies include traditional applied
behavioral analysis as well as cognitive behavior modification.

Predictable From Student’s Perspective

Student with disabilities, especially those who are also ADHD, benefit from a consistent
classroom routine. One of the first, if not the first, researchers to stress the importance of
establishing a consistent routine for students with what at the time were referred to as
minimally brain injured but today would likely be labeled as learning disabled and ADHD,
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was William Cruickshank. He established self-contained classrooms for elementary school
students with attention problems that were highly structured, with carefully sequenced
and predictable activities. The following describes his belief in consistent routines:

For example, upon coming into the classroom the child will hang his hat and coat
on a given hook—not on any hook of his choice, but on the same hook every day.
He will place his lunch box, if he brings one, on a specific shelf each day. He will
then go to his cubicle, take his seat, and from that point on follow the teacher’s in-
structions concerning learning tasks, use of toilet, luncheon activities, and all oth-
er experiences. . . . The day’s program will be so completely simplified . . . that the
possibility of failure experiences will be almost completely minimized.

(Cruickshank Bentzen, Ratzeburg, & Tannhauser, 1961, p. 18)

Conclusion
A major issue facing exceptional children going forward is whether they will be able to be
taught according to the elements of special education instruction (e.g., individualized, ex-
plicit, systematic, and intensive, with appropriate amounts of corrective feedback, rein-
forcement, and predictable routines; Pullen & Hallahan, 2015; Zigmond & Kloo, 2017). In
practice, more students with disabilities are spending more time in general education set-
tings. The U.S. Department of Education’s Annual Reports reflect this trend (see Figure
4). Inclusion increased substantially from 1990 to 1995, stabilized in the late 1990s, then
again increased substantially from 2000 to 2005 and 2005 to 2010, and has risen steadily
ever since. Federal law requires that a continuum of placements (e.g., general education
classrooms, special education classrooms for all or part of the day, residential settings) be
made available to students with disabilities; many schools are offering only general edu-
cation classroom placement (Maag, Kauffman, & Simpson, 2018).

Figure 4. Percentage of students with disabilities


in general education settings for varied amounts
of time per day.

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In keeping with the notion that the goal for exceptional children should be to increase
their placement in general education classrooms is the relatively common refrain that
“good teaching is good teaching” (Algozzine & White, 2007). However, others take excep-
tion with this as being overly simplistic (Kauffman & Konold, 2007; Pullen & Hallahan,
2015; Zigmond & Kloo, 2017). For example, Pullen and Hallahan think it best to regard
the elements, or techniques, of special education as being on a continuum, for example,
from less to more explicit and from less to more intensive. Where the student falls on the
continuum should determine whether he or she is taught by a general or a special educa-
tor and how much time he or she spends in a general or a special education classroom.
The more the instruction needed encompasses each of the techniques (e.g., explicitness,
intensity, etc.), the more likely the student should be taught by a special educator in a
special education setting. It is reasonable to maintain that there is a limit to how effec-
tively a general education teacher is able to use each of these techniques. A variety of
factors can contribute to these limitations. Chief among these influences are a teacher’s
preparation and teaching philosophy, class size, and instructional time.

Pullen and Hallahan (2015) have addressed the issue of differentiating between general
and special education instruction by posing the question:

Is special education instruction quantitatively or qualitatively different from gen-


eral education? In other words, is special education instruction merely a matter of
doing more of the same thing that’s done in general education? Or is special edu-
cation instruction somehow a different entity, with its own identity?

Special education instruction doesn’t include any techniques that can’t, and aren’t,
used by good general education instructors. However, there is a difference in the
quantity of these techniques, with respect to the degree to which they’re used, the
regularity of their use, and how many different techniques are used. And it’s the
greater quantity that makes special education differ from general educa- tion; it’s
what makes special education qualitatively different from general educa- tion; it’s
what gives special education its own identity; it’s what makes special ed- ucation
special. (p. 42)

In conclusion, it is imperative that schools abide by IDEA’s mandate of providing a contin-


uum of placements ranging from decidedly separate to highly integrated with general ed-
ucation classrooms.

Further Reading
Barkley, R. A. (2018). Attention-deficit hyperactivity disorder: A handbook for diagnosis
and treatment (4th ed.). New York: NY: Guilford.

Burack, J. A., Hodapp, R. M., Iarocci, G., & Zigler, E. (2012). The Oxford handbook of in-
tellectual disability and development. Oxford, U.K.: Oxford University Press.

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Exceptional
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Cook, B. G., Tankersley, M., & Landrum, T. J. (Eds.). (2016). Instructional practices with
and without empirical validity. Advances in Learning and Behavioral Disabilities (Vol. 29).
Bingley, U.K.: Emerald.

Hallahan, D. P., Kauffman, J. M., & Pullen, P. C. (2019). Exceptional learners: An introduc-
tion to special education (14th ed.). Upper Saddle River, NJ: Pearson Education.

Kauffman, J. M. Hallahan, D. P., & Pullen, P. C. (Eds.). (2017). Handbook of special educa-
tion (2nd ed.). New York, NY: Routledge.

Kauffman, J. M. Hallahan, D. P., Pullen, P. C., & Badar, J. (2018). Special education: What it
is and why we need it. (2nd ed.). New York, NY: Taylor & Francis.

Pullen, P. C., & Kennedy, M. J. (Eds.). (2019). Handbook of response to intervention and
multi-tiered systems of support. New York, NY: Routledge.

Volkmar, F. R., Paul, R., Rogers, S. J., & Pelphrey, K. A. (2014). Handbook of autism and
pervasive developmental disorders (Vols. 1 and 2). New York, NY: Wiley.

Wehmeyer, M. L., & Patton, J. R. (Eds.). (2017). Handbook of international special educa-
tion. Santa Barbara, CA: Prager.

Zigmond, N. (2003). Where should students with disabilities receive special educa-
tion services? Is one place better than another?. The Journal of Special Education,
37, 193–199.

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Anastasiou, D., & Keller, C. (2017). Cross-national differences in special education: A ty-
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Daniel P. Hallahan

University of Florida; University of Virginia

Paige C. Pullen

University of Florida

James M. Kauffman

University of Virginia

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Jeanmarie Badar

Charlottesville City Schools

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