Actively Recruiting
Online Pivotal Response Treatment Training in Autism Spectrum Disorder
Led by Stanford University · Updated on 2026-04-23
44
Participants Needed
1
Research Sites
152 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a research study that will assess the effects of a Pivotal Response Treatment Online Training Course (PRT-O) for training parents of children with Autism Spectrum Disorder (ASD). The study will specifically investigate whether participants can learn to deliver PRT effectively following participation in the Online training.
CONDITIONS
Official Title
Online Pivotal Response Treatment Training in Autism Spectrum Disorder
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 2 to 5 years at the time of consent
- Diagnosed with Autism Spectrum Disorder or suspected diagnosis confirmed by Autism Diagnostic Interview-Revised
- Significant adaptive communication deficits shown by specific Vineland-3 scores and clinical severity ratings
- English-speaking parent able to consistently participate and conduct treatment in English
- Stable psychotropic medication or biomedical interventions for at least one month prior to baseline with no changes expected
- Stable treatment, speech therapy, and school placement for at least one month prior with no expected changes
- Receiving no more than 60 minutes of 1:1 speech therapy per week
You will not qualify if you...
- Primary language of the child is not English
- Parent or child diagnosed with severe psychiatric disorder or unstable medical problem
- Previous adequate trial of Pivotal Response Treatment with parent meeting fidelity of implementation at baseline
- Receiving more than 15 hours per week of in-home 1:1 Applied Behavior Analysis therapy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Stanford University
Stanford, California, United States, 94305-5719
Actively Recruiting
Research Team
E
Estefania Millan, MA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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