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NCT06362733 · ClinicalTrials.gov registry record · NA
Modified Pivotal Response Treatment for Insistence on Sameness in Autistic Youth
A NA study of Autism Spectrum Disorder and Autism, sponsored by Stanford University.
- Recruiting
- Registry status
- NA
- Development phase
- 44
- Enrollment target
- 1
- Study location
NCT06362733 is a NA study of Autism Spectrum Disorder and Autism that is actively recruiting participants, run by Stanford University. The registered enrollment target is 44 participants, below the 135-participant average among 224 other Autism Spectrum Disorder trials with a reported enrollment target (67% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06362733, a NA study of Autism Spectrum Disorder and Autism, is actively recruiting participants, sponsored by Stanford University.
- RECRUITING
- Registry status
- NA
- Development phase
- 44 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this open label trial is to examine the preliminary feasibility, acceptability, and effectiveness of a 12-week behavioral intervention program (1 hour/week) to treat insistence on sameness (e.g., difficulty tolerating changes in routine) in youth with autism spectrum disorder (ASD). Treatment will be delivered via secure telemedicine platform and consist of a combination of parent-training and parent-mediated intervention with the child.
Conditions Studied
Interventions
- BEHAVIORAL Modified Pivotal Response Treatment for Insistence on Sameness in Autistic Youth
Study Locations (1)
California
- 401 Quarry Road (Remote Study) - Stanford
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2024-07-11 |
| Est. Completion | 2026-07-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06362733
The ClinicalTrials.gov registry entry for NCT06362733 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 135-participant average among 224 other Autism Spectrum Disorder trials with a reported enrollment target (67% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Autism Spectrum Disorder appearing as the primary indexed condition, and to 1 intervention - of which Modified Pivotal Response Treatment for Insistence on Sameness in Autistic Youth is the first listed.
NCT06362733 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT06362733 about?
NCT06362733 is a clinical study titled "Modified Pivotal Response Treatment for Insistence on Sameness in Autistic Youth". The purpose of this open label trial is to examine the preliminary feasibility, acceptability, and effectiveness of a 12-week behavioral intervention program (1 hour/week) to treat insistence on sameness (e.g., difficulty tolerating changes in routine) in youth with autism spectrum disorder (ASD). T...
What is the current status of trial NCT06362733?
This trial is currently recruiting. It is a NA study. The enrollment target is 44 participants. The study started on 2024-07-11. Estimated completion is 2026-07-01.
What conditions does trial NCT06362733 study?
This clinical trial studies the following conditions: Autism Spectrum Disorder, Autism, Restricted Behavior.
What interventions are being tested in trial NCT06362733?
The interventions under investigation include: Modified Pivotal Response Treatment for Insistence on Sameness in Autistic Youth (BEHAVIORAL).
Who is sponsoring clinical trial NCT06362733?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06362733 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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