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Pivotal Response Treatment (PRT) Telemedicine

Pivotal Response Treatment Telemedicine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03045263
Acronym
PRT
Enrollment
7
Registered
2017-02-07
Start date
2017-02-02
Completion date
2018-05-03
Last updated
2020-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism Spectrum Disorder

Keywords

ASD

Brief summary

The purpose of this study is to evaluate the application of a modified version of PRT designed specifically as a parent-training model via telemedicine, with the goal of increasing access to empirically validated care. The project will feature an 18-week trial of parent training PRT via telemedicine in 12 cognitively able 3- to 6-year-old children with ASD. Intervention will focus on enhancing the following developmental skills: expressive and receptive language, play, and social interaction. Outcome measures will address changes in the aforementioned domains during structured observation and standardized assessment.

Detailed description

The purpose of this study is to evaluate the application of a modified version of PRT designed specifically as a parent-training model via telemedicine, with the goal of increasing access to empirically validated care. The project will feature an 18-week trial of parent training PRT via telemedicine in 12 cognitively able 3- to 6-year-old children with ASD. Intervention will focus on enhancing the following developmental skills: expressive and receptive language, play, and social interaction. Outcome measures will address changes in the aforementioned domains during structured observation and standardized assessment.

Interventions

Behavioral intervention for autism

Sponsors

Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
3 Years to 6 Years
Healthy volunteers
No

Inclusion criteria

* Fits age requirement: age 3-6 years * Have been diagnosed previously with ASD and meet criteria for ASD when characterized by research team. * be in good medical health * be cooperative with testing * english is a language spoken in the family * full scale IQ \> 70

Exclusion criteria

* significant hearing loss or other severe sensory impairment * a fragile health status * a history of significant head trauma or serious brain or psychiatric illness

Design outcomes

Primary

MeasureTime frame
Behavioural Intervention Rating Scale (BIRS)10 weeks

Secondary

MeasureTime frame
Client Credibility Questionnaire (CCQ)10 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026