Pivotal Response Group Treatment for Parents of Young Children With Autism

Completed · Not applicable

Conditions studied: Autistic Disorder

In brief

This is a research study examining the effectiveness of pivotal response treatment group (PRTG) in targeting language skills in young children with autism. Research has demonstrated that behavioral interventions, such as Pivotal Response Training (PRT), lead to improvements in the core symptoms of autism. The purpose of this study is to further examine the effectiveness of teaching pivotal response treatment to parents of children with autism in a group format. To determine the effectiveness of pivotal response training group (PRTG) it will be compared to another parent education group by conducting a randomized controlled 12-week trial.

Key facts

Study ID

NCT01881750

Run by

Stanford University

People needed

53

Starts

2010-07-01

Expected to finish

2012-07-01

Last updated by the study team

2019-08-16

Who can join

Age: 2 and older, up to 6. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosis of Autism Spectrum Disorder (ASD) based on Autism Diagnostic Interview - Revised (ADI-R), Autism Diagnostic Observation Schedule (ADOS), Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV), and expert clinical opinion
• Outpatients between 2.0 and 6 years of age of either gender
• Children of all cognitive levels will be included as long as they are able to participate in the testing procedures to the extent that valid standard scores can be obtained
• Language delay as measured by the Preschool Language Scale 4th ed. (PLS-4)
• Participants must have the ability to make meaningful vocalizations, defined as the ability to make contingent vocalizations when prompted (i.e., vocal sound showing intent to communicate, but not necessarily clear words)
• Stable psychotropic medication(s) or biomedical interventions for at least one month prior to baseline measurements with no anticipated changes during study participation
• Stable behavioral treatment (Applied Behavioral Analysis, Floortime, or other interventions), speech therapy, and school placement for at least 2 months prior to baseline measurements with no expected changes during study participation
• No more than 60 minutes of 1:1 speech therapy per week
• The availability of at least one parent who can consistently participate in the group treatment and related activities of the research study
• Be male or female in good medical health
• Will be starting PRTG after the first magnetic resonance image (MRI) scan has occured and, if agreeable, blood draw or saliva sample
• Parents intend on continuing PRTG for a minimum of 12 weeks
• Parents must be 18 years of age or older.

You may not qualify if…

• A current or life-time diagnosis of severe psychiatric disorder (e.g., bipolar disorder…)
• A genetic abnormality, such as Fragile X, based on genetic testing, done as indicated
• Presence of active medical problem (e.g., unstable seizure disorder or heart disease)
• Participants taking psychotropic medications will not be included if their medications have not been stable for over a week
• Parents who do not have the ability to videotape parent and child interactions on a weekly basis
• Parents who are not willing to implement intervention strategies for at least one hour a day
• Parents who plan to alternate which parent attends the group sessions.

Where it is running

• Stanford University School of Medicine — Stanford, California, United States

Full record on ClinicalTrials.gov

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