- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04953793
High School SUCCESS: Vocational Soft Skills Program for Transition-Age ASD Youth (TAY SUCCESS)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Aim: With our ACHIEVE partners , develop the High School Supported, Comprehensive Cognitive Enhancement and Social Skills (SUCCESS) program to fit the needs of transition-age youth with ASD within the community educational system.
- Standardize the TAY SUCCESS program by developing a facilitator manual, student workbook and corresponding support person materials.
- Develop a training protocol that can be individualized and implemented within the HS educational system to provide initial training and ongoing coaching for educators to reach and sustain intervention fidelity.
Aim: Conduct a pilot study to examine the feasibility, acceptability, and implementation procedures (recruitment, randomization, retention & training strategies) of TAY SUCCESS and to obtain estimates of effects to support a future large-scale effectiveness trial.
- Examine intervention feasibility, acceptability, satisfaction, and sustainability.
- Examine preliminary outcomes (executive functioning and social functioning)
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
California
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San Diego, California, United States, 92123
- Rady Children's Hospital San Diego
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- autism spectrum disorder
- 15-22 yrs
- communicative English language
- enrolled in participating high school or transition program
Exclusion Criteria:
- intellectual disability
- Other significant mental health
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: TAY SUCCESS intervention
This intervention group received the TAY SUCCESS intervention over the course of 1 school year approximately 30 sessions.
|
TAY SUCCESS stands for transition age youth supported, comprehensive cognitive enhancement and social skills.
The cognitive-behavioral intervention teaches a number of strategies for executive functioning, social cognitive functioning and social communication.
|
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Active Comparator: Usual Care
This usual care group received typical High school or transition program curriculum over the course of 1 school year.
|
Usual care involved the typical vocational supportive education program delivered in the educational setting
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Behavior Rating Inventory of Executive Function (BRIEF-2/BRIEF-A)
Time Frame: baseline to 6 month post
|
Self and Parent report of executive functioning skills.
Higher scores indicate more executive functioning problems
|
baseline to 6 month post
|
|
Delis Kaplan Executive Function Scale (DKEFS)
Time Frame: baseline to 6 month post
|
performance based measure of executive functioning skills.
Higher scores indicate more executive functioning abilities
|
baseline to 6 month post
|
|
Social Responsiveness Scale 2 (SRS-2)
Time Frame: baseline to 6 month post
|
parent report social functioning scale.
Higher scores indicate more social functioning problems
|
baseline to 6 month post
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R34MH111491 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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