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NCT04899544 · ClinicalTrials.gov registry record · NA

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

A NA study of Autism Spectrum Disorder and Autism, sponsored by Stanford University.

Recruiting
Registry status
NA
Development phase
120
Enrollment target
1
Study location

NCT04899544 is a NA study of Autism Spectrum Disorder and Autism that is actively recruiting participants, run by Stanford University. The registered enrollment target is 120 participants, below the 135-participant average among 224 other Autism Spectrum Disorder trials with a reported enrollment target (11% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04899544, a NA study of Autism Spectrum Disorder and Autism, is actively recruiting participants, sponsored by Stanford University.

RECRUITING
Registry status
NA
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

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 receiving treatment as usual (TAU).

Interventions

  • BEHAVIORAL Center-Based Pivotal Response Treatment (PRT) Intervention (PRT-C)
  • BEHAVIORAL Home-Based Pivotal Response Treatment (PRT Intervention (PRT-H)

Study Locations (1)

California

  • Stanford University School of Medicine - Stanford

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2022-10-18
Est. Completion 2028-09-15
Phase NA

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT04899544

The ClinicalTrials.gov registry entry for NCT04899544 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 120 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 (11% 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 2 interventions - of which Center-Based Pivotal Response Treatment (PRT) Intervention (PRT-C) is the first listed.

NCT04899544 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT04899544 about?

NCT04899544 is a clinical study titled "Trial of Center-Based vs. In-Home Pivotal Response Treatment (PRT) in Autism". 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...

What is the current status of trial NCT04899544?

This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2022-10-18. Estimated completion is 2028-09-15.

What conditions does trial NCT04899544 study?

This clinical trial studies the following conditions: Autism Spectrum Disorder, Autism, ASD.

What interventions are being tested in trial NCT04899544?

The interventions under investigation include: Center-Based Pivotal Response Treatment (PRT) Intervention (PRT-C) (BEHAVIORAL), Home-Based Pivotal Response Treatment (PRT Intervention (PRT-H) (BEHAVIORAL).

Who is sponsoring clinical trial NCT04899544?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04899544 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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.