Actively Recruiting

Phase Not Applicable
Age: 15Years - 21Years
All Genders
NCT06552286

STRW-T Intervention for Autistic Adolescents in 11th and 12th Grade

Led by Children's Hospital Medical Center, Cincinnati · Updated on 2026-03-18

192

Participants Needed

2

Research Sites

285 weeks

Total Duration

On this page

Sponsors

C

Children's Hospital Medical Center, Cincinnati

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The current study seeks to compare outcomes of a telehealth intervention targeting daily living skills (Surviving and Thriving in the Real World - Telehealth, or STRW-T) intervention to a control group telehealth intervention targeting social skills (Program for the Education and Enrichment of Relational Skills- Telehealth, or PEERS-T). The key endpoint will be change in daily living skills on primary and secondary outcome measures at the end of treatment.

CONDITIONS

Official Title

STRW-T Intervention for Autistic Adolescents in 11th and 12th Grade

Who Can Participate

Age: 15Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • In the last 2 years of high school or deferring graduation
  • Diagnosis of autism spectrum disorder based on clinical judgement or Autism Diagnostic Observation Schedule, 2nd Edition
  • Full scale IQ of 70 or above measured by the Wechsler Abbreviated Scale of Intelligence, 2nd Edition
  • Deficient daily living skills on the Vineland Adaptive Behavior Scales, 3rd Edition with at least one subdomain 15 points below full scale IQ
Not Eligible

You will not qualify if you...

  • Significant aggressive behaviors or mental health issues requiring treatment beyond this intervention
  • Previous completion of the social skills group (PEERS) unless it was 2-3 years ago or approved by the principal investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

University of North Carolina - Chapel Hill

Carrboro, North Carolina, United States, 27510

Actively Recruiting

2

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, United States, 45229

Actively Recruiting

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Research Team

C

Carrie Fassler

CONTACT

A

Amie Duncan, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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