N/A
N=27
Development of a Family-Based Transition Planning Program for Culturally-Diverse Youth on the Autism Spectrum
Autism Spectrum Disorder · Family Relations
Bottom Line
View on ClinicalTrials.gov: NCT05965648 ↗Enrolled (actual)
27
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcome: Primary: Families FORWARD Program Acceptability Form — 52.00; 47.75 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Families FORWARD (Focusing on Relationships, Well-being, and Responsibility aheaD) (Behavioral)
- Age
- Pediatric, Adult, Older Adult · 14+ yrs
- Sex
- All
- Sponsor
- Boston University Charles River Campus
- Primary completion
- Sep 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Families FORWARD Program Acceptability Form |
52.00; 47.75 | — |
| PRIMARY Transition Planning Activities Measure |
46.08 | — |
Summary
The goal of this clinical study is to develop a community-based program to support family members of transition-aged youth on the autism spectrum to help them plan for the future. The main aims of the study are:
1. To develop the Families FORWARD program
2. To conduct proof-of-concept testing of the Families FORWARD program
Participants will complete surveys before and after participating in the program and will participate in exit interviews at the end of the program.
Eligibility Criteria
Inclusion Criteria
- Family Inclusion Criteria
- Parents or primary caregivers of transition-aged youth on the autism spectrum:
- Have one or more child(ren) on the autism spectrum who is/are ages 14-21 years old
- Identify as the parent, legal guardian, and/or primary caregiver of the youth
- Speak English fluently
- Reside in Massachusetts
- Youth on the autism spectrum:
- Have an autism diagnosis OR identify as autistic
- Age 14-21
- Have ability to communicate verbally or in written format in English
- Reside in Massachusetts
Exclusion Criteria: none
Data sourced from ClinicalTrials.gov (NCT05965648). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.