Adolescent Social Skills Training Program (ASST)
Recruitment status was: Active, not recruiting
|Asperger's Disorder High-functioning Autism||Behavioral: Multi-Media Social Skills Training Program|
|Study Design:||Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Official Title:||The Multi-media Social Skills Project: Validation of an Intervention for Adolescents With Autism Spectrum Disorders|
- Social Fluency [ Time Frame: 12 week, 3 month ]
- Loneliness Scale (Asher & Wheeler, 1985) [ Time Frame: 12 week, 3 month ]
- Social Responsiveness Scale (SRS; Constantino, 2002) [ Time Frame: 12 week, 3 month ]
- Strengths and Difficulties Questionnaire (SDQ; Goodman, 1997) [ Time Frame: 12 week, 3 month ]
|Study Start Date:||November 2009|
|Estimated Study Completion Date:||April 2011|
|Estimated Primary Completion Date:||December 2010 (Final data collection date for primary outcome measure)|
Experimental: Social Skills Training
All participants will take part in this arm of the study.
Behavioral: Multi-Media Social Skills Training Program
All individuals will participate in a twelve week social skills training program designed to enhance the social skills of adolescents with Asperger's Disorder or high-functioning autism. The intervention is comprised of both group therapy and peer generalization.
After consent , has been obtained, parents will complete the Autism Disorders Interview-Revised (ADI-R; Rutter & LeCourteur, 1995) to determine eligibility and the Checklist for Autism Spectrum Disorder (Mayes & Calhoun, 1999), the Social Responsiveness Scale (SRS; Constantino, 2002), and the Strengths and Difficulties Questionnaire (SDQ; Goodman, 1997) at the initial appointment with the study coordinator.
After assent has been obtained, adolescents will complete the Kaufman Brief Intelligence Test, Second Edition (KBIT-2; Kaufman & Kaufman, 1990) to determine eligibility and the Checklist for Autism Spectrum Disorder (Mayes & Calhoun, 1999), the Strengths and Difficulties Questionnaire (SDQ; Goodman, 1997) and the Loneliness Scale (Asher & Wheeler, 1985). Adolescents will also complete a standardized joint attention assessment.
After the completion of the eligibility and pre-test interventions there will be a wash of participants who do not meet eligibility requirements.
One week before the start of the program, participants will attend an introduction session to the program. At this time, participants will be filmed in a brief interaction with a typically developing peer that will be used as a baseline indicator of their social fluency.
Participants will attend the social skills intervention program once a week for twelve weeks. Each week there will be approximately 90 minutes of group therapy which will be conducted like a seminar class: the principal investigator will teach and review social interaction skills and nuances, participants will be encouraged to take an active role in the class.
During the twelve week intervention there will be three review/fluency building sessions: week four, week eight, and week twelve. The group therapy sessions for these review weeks will simply review the material that was covered during the prior three weeks. Participants will then practice what they have learned by having a conversation with a peer that will be taped.
Following the group therapy session each week, participants will join six typically developing peers in a 90 minute introductory photography class taught by one of the study's co-investigators. The photography class will give the participants the opportunity to practice the skills learned in group therapy with their peer group.
Participants will once again complete a battery of clinical and self-report outcome measures which will serve as the post-test measurements for the study. They will be filmed in a brief interaction with a typically developing peer which will be coded to obtain post-test social interaction skills and fluency scores. These evaluations will occur at completion of social skills program, and at three month follow-up.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01031823
|United States, Pennsylvania|
|Penn State College of Medicine, Penn State Milton S. Hershey Medical Center|
|Hershey, Pennsylvania, United States, 17033|
|Principal Investigator:||Micheal J Murray, M.D.||Penn State College of Medicine, Penn State Milton S. Hershey Medical Center|