- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05017779
A Hybrid Effectiveness-implementation Trial of a High School-based Executive Function Treatment for Autistic Youth
October 13, 2023 updated by: Cara Pugliese, Children's National Research Institute
A Hybrid Effectiveness-implementation Trial of a School Based Executive Function Treatment for Transition Age Autistic Youth
This study will test the effectiveness of a school-based cognitive behavioral executive function (EF) intervention, Unstuck & On Target High School (UOT:HS), for transition-age youth with autism spectrum disorder (ASD).
UOT:HS was designed to be embedded in high schools and delivered by school staff to improve generalization of skills, increase access to mental health care, and fill a gap in evidence-based approaches to support postsecondary transition.
UOT:HS targets flexibility and planning skills and focuses on key functions needed for adult success across 25, 1-hour lessons.
School staff will be trained to deliver UOT:HS, study staff will provide ongoing check-ins, and parents will be offered home extensions for each lesson and two trainings to generalize skills to the home environment.
Behavioral and parent-report data will be collected prior to intervention, post-intervention, and at 4-to-6-month follow-up.
Study Overview
Status
Enrolling by invitation
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
224
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Maryland
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Rockville, Maryland, United States, 20850
- Center for Autism Spectrum Disorders, Children's National Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 22 years (Child, Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- full scale IQ > 80 on a standardized IQ test, either confirmed through educational testing within the last two years or confirmed by the WASI-2 administered by research personnel. Students with a verbal IQ above 75 will be considered for inclusion based on a discussion with teacher guided by probes related to pragmatic language that align with verbal demands of the curriculum.
Two of the following:
- eligible and/or receiving school-based services or supports for autism
- a prior clinical diagnosis of autism from a qualified health professional (as indicated by parent report)
- a score of > 7 on the Social Communication Questionnaire via parent report and/or a score of > 11 via teacher report
- a score of > 6 on the Autism Spectrum Quotient-10 via self-report
- capacity to benefit and understand unstuck material as determined by teacher
Exclusion Criteria:
- Students must have a level of proficiency in English to complete questionnaires and study procedures in English. Parents must have a level of proficiency in English or Spanish to complete questionnaires and study procedures in English or Spanish.
- Student is not able to participate in UOT:HS due to their schedule or ability to benefit from curriculum material as determined by teacher.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention (Unstuck & On Target: High School)
School staff will receive training on the Unstuck and On Target: High School (UOT:HS) curriculum, and deliver lessons to students during the school day.
Interventionists will have the option to participate in ongoing check-ins with study staff.
Parents are provided home extensions for each lesson and have the option to participate in trainings delivered by study staff to support generalization of skills to the home environment.
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Unstuck & On Target: High School (UOT:HS) is a group-based curriculum for high school students that targets executive function skills using Cognitive Behavior Therapy (CBT) techniques.
UOT:HS focuses on key functions needed for adult success, such as: self-advocacy, flexibility, time management, motivation, goal setting, developing plans, monitoring progress.
Guided practice begins with concrete interventionist support and moves to interventionist cueing, self-cueing, and finally automatic use of the skills without support.
Lessons are delivered by school personnel within the school setting.
Home extension activities are provided to parents.
Other Names:
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Other: Usual Care
Participants in schools assigned to the TAU condition will continue to receive the standard school-based Individualized Education Plan (IEP) accommodations and school supports that would typically be provided.
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Participants in schools assigned to the Treatment as Usual (TAU) condition will continue to receive the standard school-based IEP accommodations and school supports that would typically be provided.
Data will be collected on the types of supports TAU schools offer, and what supports TAU students receive.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Adaptive Behavior (at follow-up)
Time Frame: Baseline, End of Intervention, Follow-up (approx. 6 months after end of intervention)
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Change in adaptive behavior will serve as the primary outcome at follow-up (e.g., approximately six month after end of intervention).
Adaptive behavior will be measured via parent-report on the Adaptive Behavior Assessment System, Third Edition (ABAS-3).
The ABAS-3 is a well-validated parent report measure that assesses practical, everyday skills needed to effectively and independently take care of oneself and interact with others across the lifespan.
Performance is represented as standard scores, with higher scores indicating better adaptive skills.
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Baseline, End of Intervention, Follow-up (approx. 6 months after end of intervention)
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Classroom Behavior
Time Frame: Baseline to End of Intervention (up to end of academic year, approx 9 months)
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Change in Classroom Behavior will serve as the primary outcome at end of intervention.
Classroom behavior will be assessed through 15-minute classroom observations conducted by a trained research staff member masked to treatment condition.
Observations will occur during the school day in an academic (non-intervention) class.
Raters use a standardized form to detect the presence or absence of seven observable behaviors: social appropriateness, on task behavior, initiation, transitions, organization, getting stuck/preservation, expression of overwhelm/negativity.
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Baseline to End of Intervention (up to end of academic year, approx 9 months)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Adaptive Behavior (end of intervention)
Time Frame: Baseline, End of Intervention (up to end of academic year, approx 9 months)
|
Change in adaptive behavior will serve as the secondary outcome at the end of intervention.
Adaptive behavior will be measured via parent-report on the Adaptive Behavior Assessment System, Third Edition (ABAS-3).
The ABAS-3 is a well-validated parent report measure that assesses practical, everyday skills needed to effectively and independently take care of oneself and interact with others across the lifespan.
Performance is represented as standard scores (mean=100; SD=15), with higher scores indicating better adaptive skills.
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Baseline, End of Intervention (up to end of academic year, approx 9 months)
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Behavior Rating Inventory of Executive Function, Second Edition (BRIEF-2)
Time Frame: Baseline, End of Intervention, Follow-up (approx. 6 months after end of intervention)
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The "Behavior Rating Inventory of Executive Function, Second Edition" (BRIEF-2) is a well-established parent-report measure of real-world EF skills, with the Shift subscale measuring cognitive flexibility.
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Baseline, End of Intervention, Follow-up (approx. 6 months after end of intervention)
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Executive Function Challenge Task (EFCT)
Time Frame: Baseline to End of Intervention (up to end of academic year, approx 9 months)
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The "Executive Function Challenge Task" (EFCT) is an objective and ecologically valid task developed by our research team to assess flexibility and planning skills in a social context conducted by a trained research staff member masked to treatment condition.
The EFCT uses a standardized, semi-structured protocol which does not provide explicit rules for completing the tasks to mimic the implicit, unspoken, unstructured expectations in everyday life.
The EFCT consists of challenges across several activities and responses are scored on a 3-point scale for each task.
The scale (0-good, 1-intermediate, 2-poor performance) has task-specific behavioral markers to guide scoring.
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Baseline to End of Intervention (up to end of academic year, approx 9 months)
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Dimensional Change Card Sort - NIH Toolbox
Time Frame: Baseline to End of Intervention (up to end of academic year, approx 9 months)
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The Dimensional Change Card Sort (DCCS) (NIH Toolbox) is a 4-minute, standard lab-based task for assessing cognitive flexibility in terms of set-shifting.
Participants are required to sort a series of bivalent cards first according to one dimension (e.g., color) and then according to another (e.g., shape).
It is normed from ages 4-85.
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Baseline to End of Intervention (up to end of academic year, approx 9 months)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Cara Pugliese, PhD, Children's Research Institute, Children's National Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 7, 2021
Primary Completion (Estimated)
October 30, 2024
Study Completion (Estimated)
November 30, 2024
Study Registration Dates
First Submitted
July 27, 2021
First Submitted That Met QC Criteria
August 18, 2021
First Posted (Actual)
August 24, 2021
Study Record Updates
Last Update Posted (Actual)
October 17, 2023
Last Update Submitted That Met QC Criteria
October 13, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01MH124772 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
De-identified individual data that supports the results will be shared via the National Institute of Mental Health's National Data Archive (NDA).
IPD Sharing Time Frame
Descriptive/raw de-identified data will be reported semi-annually through NDA.
IPD Sharing Access Criteria
Request login access to NDA data
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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