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NCT06362733Recruiting

Modified Pivotal Response Treatment for Insistence on Sameness in Autistic Youth

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
44 (estimated)
First submitted
19 Mar 2024
Start date
11 Jul 2024
Primary completion date
1 Jul 2028
Lead sponsor
Stanford University
Diseases
Autism
NCT number
NCT06362733

What you commit to

  • Study type: Interventional
  • Planned participants: 44
  • From 11 Jul 2024 to the primary completion date, 1 Jul 2028
  • 1 site 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.

Criteria the registry did not label

  • Participants will include children with:
  • parent/guardian aged 18 years or older with a child aged between 4.0 to 17.11 years old at the time of parental consent;
  • diagnosed with ASD (based on history, review of available medical records including diagnostic testing, e.g., ADOS) or suspicion of ASD diagnosis and confirmed with Autism Diagnostic Interview-Revised (ADI-R);
  • parent-reported clinically significant concerns regarding insistence on sameness and behavioral inflexibility;
  • stable behavioral and pharmacological treatment for at least two weeks with no anticipated changes;
  • English-speaking parent and youth able to consistently participate in study procedures;
  • family resides in United States.

Age in the registry: 4 years to 17 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
401 Quarry Road (Remote Study)
Coordinator of this site? Confirm its status
StanfordUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.