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Project Independence

The Development and Evaluation of an Online, Caregiver-Directed Single Session Intervention for Building Independence in Daily Living Skills in Autistic Youth

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07572110
Enrollment
70
Registered
2026-05-07
Start date
2026-05-08
Completion date
2027-12-01
Last updated
2026-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Accommodation, Autism, Daily Activities, Independence

Brief summary

This project aims to develop and test the feasibility, acceptability, and preliminary impact of a brief, online single-session intervention (SSI) for caregivers of autistic youth ages 10 to 14. The SSI, called Project Independence, is designed to give caregivers practical tools to support greater independence in daily living routines. To test the SSI, participants will be randomly assigned to either complete Project Independence or watch a time-matched, series of educational video with unrelated content.

Interventions

BEHAVIORALProject Independence

Participants will complete a self-guided, online, single-session digital intervention delivered through interactive audiovisual content. The intervention includes guided readings related to caregiving and independence, brief demonstration stories or videos, and structured reflection or brainstorming activities, lasting approximately 30 minutes.

Sponsors

University of Miami
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Any adult (age 18+) who is a parent, family member, or legal caregiver and is one of the main adults responsible for the daily care of an autistic youth in the targeted age range for at least half of the time. * Those that currently reside in the United States * Those that have a mobile device (e.g., laptop, tablet, smartphone) or desktop computer and internet access sufficient for the delivery of the study assessments and online intervention * Those who may or may not report current clinically significant psychopathological symptoms (e.g., anxiety, depression, parental stress).

Exclusion criteria

* Adults unable to consent * Individuals who are not yet adults (i.e., infants, children, teenagers).

Design outcomes

Primary

MeasureTime frameDescription
Perceived Change in Caregiver ConfidenceBaseline (pre-intervention), immediately post-intervention (same session)Caregivers will rate their perceived confidence in their ability to support their child in building independence in daily living skills using an 11-point rating scale (developed for the purpose of this study), from 0 ("Not at All Confident") to 10 ("Extremely Confident"). Higher ratings on this item indicate greater perceived confidence to support youth independence in daily living skills.

Secondary

MeasureTime frameDescription
Perceived Change in Caregiver AccommodationImmediately post-intervention, 2-week follow-upCaregivers will rate the extent to which they provided accommodation in the past week when the identified daily living skills was being completed using an 11-point rating scale (developed for the purpose of this study), from 0 ("Not at all") to 10 ("Completely"). Higher ratings on this item indicate greater perceived accommodation use in the identified daily routine.
Perceived Change in Opportunities for Youth Practice in IndependenceImmediately post-intervention, 2-week follow-upCaregivers will rate how often they provided opportunities for their child to practice the identified daily living skill independently using an 11-point rating scale (developed for the purpose of this study), from 0 ("Never") to 10 ("Almost Always"). Higher ratings on this item indicate greater perceived opportunities provided to youth to practice independence the identified daily routine.
Program Feedback Scale (PFS)Immediately post-interventionParticipants will complete the Program Feedback Scale (PFS), an 8 item validated self report measure assessing perceived acceptability and feasibility of the intervention. Items are rated on a 5 point Likert scale ranging from 1 ("Really disagree") to 5 ("Really agree"), with higher scores indicating greater perceived acceptability and feasibility.

Countries

United States

Contacts

CONTACTSandra L Cepeda, M.S.
slc247@miami.edu305-284-2712
PRINCIPAL_INVESTIGATORJill Ehrenreich-May, Ph.D.

University of Miami

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026