NCT04146428Completed
Evaluating BOSCC and ELSA as Outcome Measures in the Context of a JASPER Intervention Trial
Source: ClinicalTrials.gov · Last updated 28 Jan 2026
Brief summary (registry, in English)
Research teams in Boston University, UCLA, and Weill Cornell will recruit 90 participants in 3 years (10 participants per site per year) and evaluate JASPER, play-based intervention, using the BOSCC and ELSA-T. Participants will be randomized to receive JASPER facilitated either by a clinician or the caregiver. After 10 weeks, the participants will be evaluated using the CGI to determine if they are "responders" or "non-responders". Nonresponders will be given a mix of clinician and caregiver-facilitated JASPER and responders will remain the course for the following 10 weeks. Coding of the BOSCC and ELSA-T will be the outcome measures and change will be evaluated throughout the study.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 84 (actual)
- First submitted
- 29 Oct 2019
- Start date
- 27 Apr 2021
- Primary completion date
- 14 May 2025
- Lead sponsor
- University of California, Los Angeles
- Diseases
- Autism
- NCT number
- NCT04146428
What you commit to
- Study type: Interventional
- Participants enrolled: 84
- From 27 Apr 2021 to the primary completion date, 14 May 2025
- 4 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- Children that do not have a mental age greater than or equal to 12 months, don't have a confirmed diagnosis, are under the age of 18 months and older than 5 years of age.
Who the study is looking for
- Minimally verbal children eligible for the ADOS Toddler Module or Module 1 (pre or minimally verbal) or those who have emerging phrases who may receive Module 2 (phrase speech) will be enrolled. The sample will be limited to children with confirmed diagnosis and nonverbal mental ages greater than or equal to 12 months. The child must be 18 months and 5 years of age.
Age in the registry: 18 months to 5 years · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Boston University Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| UCLA Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Semel Institute Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Weill Cornell Medical College/New York Presbyterian Hospital Coordinator of this site? Confirm its status | White Plains | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.