Evaluating wraparound services for seriously emotionally disturbed youth: pilot study outcomes in Georgia.
Copp, Hilary L. ; Bordnick, Patrick S. ; Traylor, Amy C. 等
In the United States, nearly 21% of children and adolescents aged
9-17 are diagnosed with a mental health or addictive disorder that
causes at least minimal impairment in daily functioning (U.S. Department
of Health and Human Services [USDHHS], 1999). The most prevalent
diagnoses are anxiety disorders (13%), disruptive disorders (10.3%), and
mood disorders (6.2%) (USDHHS, 1999). Approximately 9-13% of all
children and adolescents (6-9 million) are diagnosed with a severe
emotional disturbance [SED] (Friedman et al., 1996), a legal term
defined in 1993 by the Substance Abuse and Mental Health Services
Administration [SAMHSA] as:
Persons from birth up to age 18 who currently or at any time during
the past year had a diagnosable mental, behavioral, or emotional
disorder of sufficient duration to meet diagnostic criteria
specified within the DSM-III-R, and that resulted in functional
impairment which substantially interferes with or limits the
child's role or functioning in family, school, or community
activities (p. 29425).
These children may have legal, school, family, and social problems
and require services from a number of different providers, but families
are often left without the proper resources to manage the disorders or
provide care for their child(ren) across service agencies. Navigating
the many agencies providing services can be a daunting or impossible
task for parents and caregivers. This approach leads to gaps in care and
results in a lack of cohesion of services, leaving families without
necessary resources. Given these serious issues, families of children
with SEDs are in need of a comprehensive system of care to provide
coordination of care.
In response to this need for coordination, the Substance Abuse and
Mental Health Services Administration (SAMHSA) in the U.S. Department of
Health and Human Services initiated the Comprehensive Community Mental
Health Services for Children and Their Families Program in 1992 so as to
provide grants to establish local systems of care for children with SEDs
and their families in select communities throughout the U.S. and its
territories; to date, 92 programs have been funded (USDHHS, 2004). The
system of care model is based upon four primary concepts: that services
should be family-centered and strengths-based; that services should be
collaborative and community-based; that services should be culturally
appropriate; and that families should be partners in the system of care
(USDHHS, 2004). In 2001, SAMSHA awarded one such grant to a site in
Georgia, where services were intended to serve families in three rural
counties.
The SAMSHA Wraparound System of Care model is the largest mental
health initiative ever undertaken in the United States, in terms of
financing and scope. It has been widely adopted to deal with
children's emotional problems, educational deficiencies, and
juvenile delinquency issues (e.g., Hansen, Litzelman, Marsh, &
Milspaw, 2004; Huffine, 2002; Walker & Schutte, 2004) and is
beginning to have an impact on graduate training programs in the human
services (e.g., Herrick, Arbuckle, & Claes, 2002). Relatively few
empirical evaluations of comprehensive wraparound services appear to
have been published, which is a conspicuous omission given the
considerable public resources that have been expended on promulgating
this model. Those that have been conducted seem to find comparatively
few improvements among those children and families receiving wraparound
services in comparison to those exposed to treatment-as-usual care
available via the public educational, social service, mental health, and
juvenile justice systems (Bickman, Smith, Lambert, & Andrade, 2003;
Carney & Buttell, 2003).
This paper focuses on three primary objectives of the initial
evaluation efforts for the Georgia site. The first objective was to
examine the feasibility of implementing a comprehensive computer-based
assessment protocol used to evaluate participant functioning. The second
objective was to conduct an evaluation of children and families enrolled
in the system of care at intake and at 6 months. The third objective was
to provide empirically based feedback to the system of care service
providers in order to improve program services and evaluation efforts.
METHOD
Procedures
To complete the first objective, laptop computers were loaded with
standardized evaluation/instrumentation software developed by Macro
International Inc., a private program-evaluation company that is the
primary contracted evaluator for the national wraparound demonstration
program sites. All laptop computers were synched with a web-based data
upload system (Quick SAT Version 3.1, Macro International Inc.), which
allows sites to upload evaluation data, track completion status, correct
errors, receive feedback on progress of data collection, and download
individual and cumulative reports. Three graduate-level social workers
were trained in the use of the laptop-based Macro International
software, interview protocol, clinical assessment instruments, and data
upload procedures. Upon completion of training, all interviewers were
prepared to conduct field interviews for the evaluation project.
Once the technological and training aspects of the assessment
system were in place, the second objective, conducting an evaluation of
families and children, was initiated. Children were referred to the
local system of care via schools, the Georgia Department of Juvenile
Justice, mental health agencies and other community services. Children
and families who met the system criteria for enrollment were enrolled
into the system of care. Contact information and signed release forms
for these families were then forwarded to the local university-based
evaluation team. A member of the evaluation team then contacted the
caregiver to acquire consent to enroll the family in a long-term outcome
study, with interviews to be conducted at baseline and every 6 months
thereafter with the primary caregiver and separately with the child (if
at least 11 years old). Eligibility requirements for the long-term study
included caregiver consent, youth assent (if 11+), enrollment in the
system of care, and child's age between 5 and 17.5 years at
baseline. Families were scheduled to be interviewed every 6 months out
to 24 months after baseline. Families were dropped from the study at the
caregiver's request or after two consecutive data collection points
were missed due to inability to contact the family, caregiver refusal,
family moving out of the area, or other experience that prohibited data
collection. All study procedures were approved by the University of
Georgia Institutional Review Board, and adhered to the national
assessment and evaluation protocol developed by Macro International,
Inc.
Interviews were conducted at the family's home and took
between 2 and 4 hours to complete. Interviewers utilized laptop
computers to administer 9 assessment instruments and descriptive
questionnaires to caregivers at baseline (11 at follow-up), and when
appropriate, 5 instruments to youth at baseline (6 at follow-up).
Subjects were paid $10/hour for interview time. This paper reports data
from 2 of the caregiver instruments administered as part of both the
baseline and 6-month interviews.
Participants
A total of 45 children were enrolled in the Georgia wraparound
system of care demonstration study between October 2001 and May 2004.
Complete baseline and 6-month follow-up data reported by caregivers are
available for only 15 children, whose data are reported in this paper.
Of these 15 children, 8 (53.3%) were male and 7 (46.7%) are female. Six
(40%) are African American, 8 (53.3%) are White, and 1 (6.7%) Mexican).
Seven of the 15 (46.7%) were between ages 8 and 10 years at the time of
their baseline interview and therefore ineligible for a youth interview.
The remaining 8 (53.3%) were between ages 11 and 14 years at baseline.
The mean age at intake was 10.5 years.
Participants reported between 2 and 23 total problems leading to
referral to the system of care. One participant (6.7%) reported 23
problems; 5 participants (33.3%) reported 10-15 problems, and the
remaining 9 participants (60%) reported 2-8 problems. Those most
frequently reported were attention difficulties (73.3%),
hyperactive-impulsive (66.7%), non-compliance (60%), poor self-esteem
(60%), physical aggression (53.3%), and poor peer interaction (53.3%).
Outcome Measures
The Child Behavior Checklist for Ages 4-18 (CBCL; Achenbach, 1991)
is a 113-item questionnaire administered to the child's caregiver.
The caregiver indicates whether the child displays certain behaviors,
such as "Cruel to animals," "Feels worthless or
inferior," and "Not liked by other kids" utilizing a
3-point Likert scale (2-very true or often true; 1-somewhat or sometimes
true; 0-not true) (Achenbach & Edelbrock, 1983). The scale scores 3
Internalizing syndromes (withdrawn, somatic complaints,
anxious/depressed, 2 Externalizing syndromes (delinquent behavior,
aggressive behavior), and 3 neither Internalizing nor Externalizing
syndromes (social problems, thought problems, attention problems)
(Achenbach, 1999). Raw scores range from 0-236 and T scores range from
23-100. Scores of 64 and higher on the Total Problem, Internalizing
(total), or Externalizing (total) are considered to be in the clinical
range; scores of 60-63 are in the borderline clinical range, and scores
of 59 and less are considered to be in the normal range (Heflinger &
Simpkins, 2002). In this paper only the Total Problem, total
Externalizing and total Internalizing scores are presented. The CBCL has
been demonstrated to have high test-retest and inter-rater reliability
and construct and criterion-related validity (Achenbach & Edelbrock,
1983).
The Child and Adolescent Functional Assessment Scale (CAFAS;
Hodges, 1994), used with children ages 7-17 years, allows clinicians or
researchers to rate a child's level of impairment across various
aspects of functioning (school/work, home, community, behavior toward
others, moods/emotions, self-harmful behavior, substance use, and
thinking) based upon the child's worst behavior during the
evaluation period (e.g., previous 3 months, 6 months). These 8 subscales
are scored from 0-30 (0-minimal or no impairment; 10-mild impairment;
20-moderate impairment; 30-severe impairment). A total score (0-240) is
also returned, with 0-10 indicating minimal or no impairment, 20-40
indicating that outpatient treatment is probably sufficient, 50-90
indicating that additional services beyond outpatient may be necessary,
100-130 indicating that more intensive care is probably necessary, and
140 and higher indicating that intensive care is probably necessary in
combination with risk and community resource assessment (Hodges, 1994).
The CAFAS has been demonstrated to have high test-retest and
inter-rater reliability (Hodges & Wong, 1996; Hodges, 1999; Hodges,
Doucette-Gates, & Liao, 1999) content and face validity (Hodges,
1999), and criterion-related and construct validity (Hodges & Kim,
2000; Hodges & Wong, 1996; Hodges et al., 1999; Hodges, 1999). The
CAFAS may be used both to evaluate individual consumers' impairment
and as a measure of treatment outcome (Hodges, 1999; Hodges & Kim,
2000; Hodges et al., 1999).
RESULTS
SPSS version 10.0 was used to run all statistical analyses (SPSS,
2001). Mean scores and standard deviations are presented in Table 1 for
the CAFAS and CBCL subscales and total scores at intake and 6-month
follow assessments. Paired t-tests examined potential differences on
these variables at the two points in time, with a Bonferroni correction used to calculate a more conservative p-value, due to the large number
of t-tests conducted. No significant differences were found on any
variable, indicating neither improvement nor deterioration in
participant functioning over this time period.
DISCUSSION
Our results failed to demonstrate any meaningful changes on outcome
measures during the first six months of participation in comprehensive
wraparound services among 15 participating children and their families
in rural Georgia. Relatively high participant attrition caused by either
our inability to recontact these families after six months, their
refusal to be re-assessed, or their dropping out of the program, makes
the representatives of our 15 participants (out of an initial cohort of
45) a potentially confounding variable. An additional factor is our
service program's failure to systematically assess adherence to the
guiding principles of wraparound services. This means that our failure
to find predicted improvements in child functioning post-intervention
cannot be unambiguously attributed to deficiencies in the wraparound
model of care, in the absence of assessing fidelity to the treatment
model itself. While our service providers were well-trained in
wraparound services, and made every effort to follow such comprehensive
system-of-care guidelines, formal assessments of treatment fidelity were
not obtained, which introduces the possibility that the independent
variable, wraparound services, may not have been provided in an
effective manner. We recommend that future program evaluations of
wraparound services make use of some system of formal fidelity checks,
such as that developed by Bruns, Burchard, Suter, Leverentz-Brady, and
Force (2004), as a potential means of controlling for this confounding
variable. Thus our failure to find improvements in participant function
may be due to actual deficiencies in the overall model of wraparound
services in living up to its hypothesized effectiveness, or to the
methodological limitations in our preliminary study of outcomes.
The goals of this evaluation focused on implementing and conducting
a comprehensive computer-based evaluation program and on providing
empirically based feedback to the agency providing wraparound services.
The first goal was to examine the feasibility of implementing a
comprehensive, computer-based assessment protocol with severely
emotionally disturbed children and their families. We found that it was
feasible, albeit with very high attrition rates. The second goal was to
conduct an outcome study of child functioning after receiving six months
of wraparound services, using standardized assessment instruments. This
was accomplished with 15 participants. Our informal observations are
that the undue length of the assessment protocol, involving over a dozen
standardized measures (only two of which are reported here), acted as a
barrier to obtaining participant cooperation, despite our provision of a
modest honorarium. Interviews ranged between 2 and 4 hours and many
questions were asked repeatedly because they were included in more than
one assessment instrument. Reducing the length of the interviews by
streamlining the questions and asking for only applicable and
nonredundant data could lead to a decrease in attrition rates as more
families may be willing to participate in the assessment process if it
did not take as long to complete.
Finally, the third goal was to provide empirically based feedback
to improve program services and evaluation efforts. Information
collected during this evaluation was presented to the Georgia service
providers, allowing them to utilize empirical data to better understand
the strengths and needs of their program. Whether this results in
improvements to the program and in its effectiveness remains to be seen.
While the "face validity" and intuitive appeal of the
general principles of comprehensive system-of-care wraparound services
for seriously emotionally disturbed youth and their families is
considerable, our sense is that the expansion of this program nationally
has exceeded the degree of empirical evidence of its effectiveness. This
is not to assert that wraparound services are ineffective, only that
smaller scale pilot studies should have been undertaken, with positive
results, prior to its widespread (and expensive) adopting. This, of
course, is a familiar refrain in the program evaluation field, where the
selection of services are sometimes driven more by ideology than by
scientific merit. While our initial outcomes in Georgia with wraparound
services are not promising, it may be that longer-term assessments may
reveal more positive results, or that with additional experience in
providing wraparound services our providers will become more effective.
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Hilary L. Copp, Patrick S. Bordnick, and Amy C. Traylor, School of
Social Work, University of Georgia.
Bruce A. Thyer, College of Social Work, Florida State University.
Reprint requests should be sent to Patrick S. Bordnick, Ph.D.,
School of Social Work, University of Georgia, Athens, GA 30602 or via
the Internet using bordnick@bellsouth.net
Table 1. Mean Scores for Intake and 6-Month Follow-up on
Outcome Measures (N = 15)
Intake 6 Month
M SD M SD t p
CBCL (raw scores)
Internalizing 17.0 9.8 15.9 7.7 0.91 0.38
Externalizing 29.1 10.0 26.9 8.9 1.38 0.19
Total Problem
Score 75.1 30.7 72.9 24.8 0.51 0.62
CBCL (T scores)
Internalizing 65.0 10.1 64.3 9.8 0.47 0.65
Externalizing 71.7 7.4 70.2 6.6 1.19 0.26
Total Problem
Score 72.1 8.6 71.5 7.4 0.44 0.66
CAFAS (raw scores)
School/Work 22.0 8.6 23.3 8.2 -1.00 0.33
Home Role 23.3 9.0 22.1 8.9 0.25 0.81
Community/
Role 4.7 7.4 4.3 7.6 -0.29 0.78
Behavior
Toward
Others 22.7 7.0 20.7 7.0 1.15 0.27
Moods/
Emotion 16.7 8.2 16.7 10.5 0.00 1.00
Self-Harm 7.3 11.6 5.3 9.2 0.90 0.38
Substance
Abuse 0.0 0.0 0.0 0.0 n/a n/a
Thinking 8.7 11.3 2.7 5.9 2.20 0.05
Total Score 105.3 37.0 93.3 28.2 1.51 0.15