- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06559267
School-based Paraeducator Education for Engagement at Recess (SPEER)
August 11, 2025 updated by: Freda Liu, University of Washington
The purpose of the proposed three-site study is to test whether an educator-level implementation strategy, coaching, with or without a school-level implementation strategy, school-based teams, will maximize paraeducators' use (fidelity and sustainment) of an evidence-based social engagement intervention, Remaking Recess (RR).
RR aims to improve peer related social skills for autistic students and their non-autistic peers who are socially isolated or peripheral and need support during recess.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
350
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 Contact
- Name: Kemmerly Chipongian
- Phone Number: 206-543-3750
- Email: chipokem@uw.edu
Study Locations
-
-
California
-
Los Angeles, California, United States, 90095
- Not yet recruiting
- University of California Los Angeles
-
Contact:
- Consuelo Garcia
- Phone Number: 310-825-4775
- Email: cogarcia@mednet.ucla.edu
-
-
Oregon
-
Eugene, Oregon, United States, 97403
- Not yet recruiting
- University of Oregon
-
Contact:
- Stephanie Shire, PhD
- Phone Number: 541-346-2141
- Email: sshire@uoregon.edu
-
-
Washington
-
Seattle, Washington, United States, 98115
- Recruiting
- University of Washington
-
Contact:
- Freda Liu, PhD
- Phone Number: (206) 987-3295
- Email: fredaliu@uw.edu
-
Contact:
- Kemmerly Chipongian
- Phone Number: (206) 543-3750
- Email: chipokem@uw.edu
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Students: Elementary aged students in K-5th grade who are autistic or have a neurodevelopmental disorder (Age 5-12)
- Educators: Paraeducators, teachers, or other school personnel that work with K-5th grade students in a public school in the United States (Age 18+)
Exclusion Criteria:
- Students or educators that have previously participated in Remaking Recess studies will not be eligible to enroll in this study.
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Remaking Recess
Remaking Recess is a school-based social engagement intervention designed to enhance elementary school contextual factors to better support peer engagement during recess.
Remaking Recess is delivered to educators through direct training and in vivo coaching by a certified Remaking Recess Coach.
|
Remaking Recess (RR) is a school-based social engagement intervention designed to enhance elementary school contextual factors to better support peer engagement during recess.
Remaking Recess is delivered to educators through direct training and in vivo coaching by a certified Remaking Recess Coach.
Other Names:
|
|
Experimental: TEAM
Schools that are randomized to the TEAM condition will receive an additional implementation support intervention.
TEAM will leverage existing human resources in the school to specifically focus on developing an implementation blueprint to foster a supportive implementation context for paraeducators to use Remaking Recess.
|
Remaking Recess (RR) is a school-based social engagement intervention designed to enhance elementary school contextual factors to better support peer engagement during recess.
Remaking Recess is delivered to educators through direct training and in vivo coaching by a certified Remaking Recess Coach.
Other Names:
Schools that are randomized to the TEAM condition will receive an additional implementation support intervention.
TEAM will leverage existing human resources in the school to specifically focus on developing an implementation blueprint to foster a supportive implementation context for paraeducators to use Remaking Recess.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Remaking Recess Fidelity
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
This 20-item observation measure rates how well educators are observed to be using core Remaking Recess strategies with students on the playground.
Minimum score 1, maximum score 5. Higher scores indicate better outcome.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Playground Observation of Peer Engagement (POPE)
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
This observation-based instrument measures children's engagement with activities and peers.
It rates children's engagement states and the frequency within a set amount of time.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
|
Friendship Survey
Time Frame: Baseline, 4 months, 8 months
|
This 5-item free response survey asking students to identify their preferred peers at school.
The results of the survey will be analyzed to identify student social network centrality in their classroom (Nuclear, Secondary, Peripheral, or Isolated).
|
Baseline, 4 months, 8 months
|
|
Teacher Perceptions Measure
Time Frame: Baseline, 4 months, 8 months
|
This 12-item measure asks teachers to report on their perceptions of their target student's social skills.
Minimum score 1, maximum score 3. Higher scores indicate better outcome.
|
Baseline, 4 months, 8 months
|
|
Acceptability of Intervention Measure (AIM)
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
This 12-item self-report measure asks educators to rate how acceptable the interventions (Remaking Recess and TEAM) were.
Minimum score 1, maximum score 5. Higher scores indicate better outcome.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
|
Cost Measure
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
This survey measure asks educators how much time they spent on study-related procedures (Remaking Recess and TEAM) each week.
The measure then calculates the average dollar cost each week of study-related procedures based off of the educator's salary in order to better understand the cost of implementation and intervention.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
|
Provider Report of Sustainment Scale (PRESS)
Time Frame: 12 months, 16 months
|
This 3-item self-report measure asks educators to reflect on the sustainment of the use of the target intervention (Remaking Recess) at their school.
Minimum score 0, maximum score 4. Higher scores indicate better outcome.
|
12 months, 16 months
|
|
School Implementation Leadership Scale (S-ILS)
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
This 25-item measure captures educator perceptions of their school leadership and how well the leadership supports the use of the intervention (Remaking Recess).
Minimum score 0, maximum score 4. Higher scores indicate better outcome.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
|
School Implementation Climate Scale (SICS)
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
This 21-item measure captures educator perceptions of their school culture and how well the intervention (Remaking Recess) fits in.
Minimum score 0, maximum score 4. Higher scores indicate better outcome.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
|
Team Process Survey Measure (TPS)
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
A 10-item self-report measure to capture team process.
Minimum score 1, maximum score 5. Higher scores indicate better outcome.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
|
Quality of Play Questionnaire
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months
|
A 19-item measure for parents/caregivers to complete about their child's playdates.
Items 1-17 are a numerical rating of how much time a child spends on an activity in their play, with score ranging from a minimum of 0 to maximum of 3. Items 18-19 are a free response numerical frequency rating for parents to report on the number of playdates their child had in the last month.
|
Baseline, 4 months, 8 months, 12 months, 16 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Freda Liu, PhD, University of Washington
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)
July 1, 2024
Primary Completion (Estimated)
August 1, 2029
Study Completion (Estimated)
August 1, 2029
Study Registration Dates
First Submitted
August 15, 2024
First Submitted That Met QC Criteria
August 15, 2024
First Posted (Actual)
August 19, 2024
Study Record Updates
Last Update Posted (Estimated)
August 15, 2025
Last Update Submitted That Met QC Criteria
August 11, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00020326
- R324A240031 (Other Grant/Funding Number: Institute of Education Sciences)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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