- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03020927
Therapist and Parent Delivered Reciprocal Imitation Training for Young Children With Autism Spectrum Disorder (ParentRIT)
April 21, 2026 updated by: Katherine Walton, Ohio State University
The purpose of this study is to examine whether adding a parent education component to an existing intervention (Reciprocal Imitation Training) results in improved outcomes for children with Autism Spectrum Disorder.
Reciprocal Imitation Training (RIT) is a behavioral intervention designed to improve spontaneous imitation skills in young children with Autism Spectrum Disorder (ASD).
Previous research suggests that it can be effective when used by trained therapists, teachers, siblings, and parents of children with ASD.
However, it is unclear to what extent training parents to use RIT strategies in the home environment may enhance outcomes, compared to having therapists implement RIT individually with the child.
The study will compare two different versions of RIT for young children with ASD: (1) two 60-minute weekly sessions of therapist-implemented RIT and (2) one weekly 60-minute session of therapist-implemented RIT and one weekly 60-minute session of parent education about using RIT in the home environment.
The investigators will examine child and family outcomes between these two intervention types.
Outcomes examined will include: (1) spontaneous and prompted imitation skills in the child with ASD, (2) social communication skills in the child with ASD, (3) parent stress, and (4) parent and child behaviors during parent-child play interactions.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
18
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ohio
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Columbus, Ohio, United States, 43210
- The Ohio State University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
2 years to 5 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- have a community diagnosis of Autism Spectrum Disorder (as reported by parent)
- meet cutoff for "Autism" or "Autism Spectrum" on the Autism Diagnostic Observation Schedule, 2nd Edition
- be between 24 and 60 months of age at the time of study enrollment
- demonstrate difficulties with imitation skills on the Motor Imitation Scales and/or the Unstructured Imitation Assessment during pre-treatment assessments
Exclusion Criteria:
- Participants must not be the sibling of another study participant
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: Therapist Delivered
Children in the therapist-delivered condition will receive two, 60-minute long sessions of Reciprocal Imitation Training each week for ten consecutive weeks.
These sessions will be delivered by trained graduate, undergraduate, and post-graduate research staff.
Parents will be permitted to observe sessions via live video, but will not be directly involved in intervention.
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Naturalistic Developmental Behavioral Intervention aimed at improving social imitation skills.
Other Names:
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Experimental: Parent + Therapist Delivered
Children in the parent + therapist-delivered condition will receive one, 60-minute long session of Reciprocal Imitation Training each week for ten consecutive weeks.
These sessions will be delivered by trained graduate, undergraduate, and post-graduate research staff.
During the same period of time, parents/guardians of children will receive one, 60-minute long parent education session per week with graduate and post-graduate research staff, aimed at teaching parents to implement Reciprocal Imitation Training at home with the child.
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Naturalistic Developmental Behavioral Intervention aimed at improving social imitation skills, using a combination of therapist-delivered intervention and parent training to deliver intervention in the home setting.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Unstructured Imitation Assessment (UIA)
Time Frame: Change from baseline to 10 weeks (immediately post-intervention)
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The Unstructured Imitation Assessment (UIA) is a semi-structured, standardized test of imitation skills containing 10 object imitation and 10 gesture imitation tasks (Ingersoll & Meyer, 2011).
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Change from baseline to 10 weeks (immediately post-intervention)
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Percentage of parent acts imitated during Parent-Child Play Interaction
Time Frame: Change from baseline to 10 weeks (immediately post-intervention)
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Percentage of parent play acts and meaningful gestures imitated by the child during a 10-minute unstructured play interaction with parent
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Change from baseline to 10 weeks (immediately post-intervention)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Parenting Stress Index, 4th Edition
Time Frame: Change from baseline to 10 weeks (immediately post-intervention)
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Change from baseline to 10 weeks (immediately post-intervention)
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Motor Imitation Scales
Time Frame: 10 weeks (immediately post-intervention), 3 months post-treatment, 6 months post-treatment
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10 weeks (immediately post-intervention), 3 months post-treatment, 6 months post-treatment
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Early Social Communication Scales
Time Frame: 10 weeks (immediately post-intervention), 3 months post-treatment, 6 months post-treatment
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10 weeks (immediately post-intervention), 3 months post-treatment, 6 months post-treatment
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Proportion of time spent jointly engaged during Parent-Child Play Interaction
Time Frame: Change from baseline to 10 weeks (immediately post-intervention)
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Proportion of time spent in joint engagement state (joint focus on same activity) during a 10-minute unstructured play interaction with parent
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Change from baseline to 10 weeks (immediately post-intervention)
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Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Modified Behavior Intervention Rating Scale
Time Frame: 10 weeks (immediately post-intervention)
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10 weeks (immediately post-intervention)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2016
Primary Completion (Actual)
August 1, 2022
Study Completion (Actual)
August 1, 2022
Study Registration Dates
First Submitted
June 3, 2016
First Submitted That Met QC Criteria
January 11, 2017
First Posted (Estimated)
January 13, 2017
Study Record Updates
Last Update Posted (Actual)
April 24, 2026
Last Update Submitted That Met QC Criteria
April 21, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015B0475
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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