Elsevier

Behavior Therapy

Volume 46, Issue 1, January 2015, Pages 7-19
Behavior Therapy

Cognitive Behavioral Therapy for Early Adolescents With Autism Spectrum Disorders and Clinical Anxiety: A Randomized, Controlled Trial

https://doi.org/10.1016/j.beth.2014.01.002Get rights and content

Highlights

  • Clinically elevated anxiety is common among adolescents with high functioning autism spectrum disorders.

  • A CBT program for youth with ASD outperformed a 4-month waitlist condition.

  • The CBT program showed greater improvement in parent-rated autism symptom severity at posttreatment compared to waitlist.

  • Comparison to an active treatment condition is a logical next step in evaluating the intervention program.

Abstract

Clinically elevated anxiety is a common, impairing feature of autism spectrum disorders (ASD). A modular CBT program designed for preteens with ASD, Behavioral Interventions for Anxiety in Children with Autism (BIACA; Wood et al., 2009) was enhanced and modified to address the developmental needs of early adolescents with ASD and clinical anxiety. Thirty-three adolescents (11–15 years old) were randomly assigned to 16 sessions of CBT or an equivalent waitlist period. The CBT model emphasized exposure, challenging irrational beliefs, and behavioral supports provided by caregivers, as well as numerous ASD-specific treatment elements. Independent evaluators, parents, and adolescents rated symptom severity at baseline and posttreatment/postwaitlist. In intent-to-treat analyses, the CBT group outperformed the waitlist group on independent evaluators’ ratings of anxiety severity on the Pediatric Anxiety Rating Scale (PARS) and 79% of the CBT group met Clinical Global Impressions–Improvement scale criteria for positive treatment response at posttreatment, as compared to only 28.6% of the waitlist group. Group differences were not found for diagnostic remission or questionnaire measures of anxiety. However, parent-report data indicated that there was a positive treatment effect of CBT on autism symptom severity. The CBT manual under investigation, enhanced for early adolescents with ASD, yielded meaningful treatment effects on the primary outcome measure (PARS), although additional developmental modifications to the manual are likely warranted. Future studies examining this protocol relative to an active control are needed.

Section snippets

Participants

The sample included 33 adolescents, ranging in age from 11 to 15 years (M = 12.3 years, SD = 1.14) and their parents, recruited through two research sites: 17 at the University of South Florida (USF) Rothman Center for Neuropsychiatry (11 males, 6 females) and 16 at the University of California–Los Angeles (UCLA) Center for Autism Research and Treatment (12 males, 4 females). Sample size was determined via power analysis, where an ES of d = 1.0 was assumed for group differences in anxiety reduction,

Results

The intent-to-treat sample size was 33. There were 2 dropouts and 1 protocol violation during the waitlist, and 1 dropout and 2 protocol violations (beginning excluded treatments or changing medication dose) during CBT (see Figure 1). Recruitment began on 9/21/2010 and ended on 6/14/2011; posttreatment assessments were completed on 12/13/2011. Table 1 presents descriptive and diagnostic information for children in the two treatment conditions. Total child DSM-IV diagnoses including ASD, anxiety

Discussion

Early adolescents with clinical anxiety may benefit from developmentally appropriate, individually administered CBT with collateral parent and school support components. A notable characteristic of the participants in this study was their overall level of concurrent psychiatric symptomology as illustrated by meeting criteria for multiple (2 to 7) comorbid diagnoses over and above their ASD diagnosis. In spite of the overall level of clinical challenge posed by concurrent ASD-related

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    This study was supported by a multisite grant awarded to Jeffrey J. Wood, Eric Storch, and Jill Ehrenreich from the National Institute of Child Health and Human Development (HD65270). We are very grateful to the participating families. We also acknowledge the contributions of Lindsay Brauer, P. Jane Mutch, Josh Nadeau, Amy Parks (University of South Florida), Michael Hernandez, Carly Schwartzman and Ilana Seager (University of Miami), and C. Enjey Lin and Kelly Decker (UCLA).

    Clinicaltrials.gov trial reference number: NCT01177969. Internet links: http://clinicaltrials.gov/ct2/show/NCT01177969

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