Trial of Center-Based vs. In-Home Pivotal Response Treatment (PRT) in Autism

Recruiting N/A Interventional Study
Autism Autism Spectrum Disorder ASD
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
2 – 5
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Stanford University · Other
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About This Trial
The aim of this clinical trial is to compare the efficacy of a 16-week center-based Pivotal Response Treatment (PRT-C) versus home-based Pivotal Response Treatment (PRT-H) in targeting social communication deficits in young children with autism spectrum disorder (ASD) with significant language delay. The two groups will also be compared to a control group that consists of children who are receivin…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Diagnosis of Autism Spectrum Disorder (ASD) based on Autism Diagnostic Interview Revised (ADI-R), Autism Diagnostic Observation Schedule, Second Edition (ADOS-2) or Childhood Autism Rating Scale, Second Edition (CARS-2), Diagnostic and Statistical Manual 5th Edition (DSM-5), a…
Contacts

Maddy Clark

(650)736-1235

PALprogram@stanford.edu

CONTACT

Beatrice Begley

(650)736-1235

PALprogram@stanford.edu

CONTACT