- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03901300
An Intervention to Improve Motor Skills in Young Children (PLAY)
PLAY: An Intervention to Improve Motor Skills in Young Children
Study Overview
Status
Intervention / Treatment
Detailed Description
Preschoolers spend 4 hours/day in front of a screen, while fewer than one-quarter engage in the recommended two hours of daily physical activity (PA). The decline in PA, increase in screen-based behaviors, and onset of obesity during preschool years have been linked to lifetime risk of obesity and related comorbidities. However, emerging evidence indicates that "screen time" can actually be leveraged as a tool to increase children's PA and promote healthy weight. Specifically, PA interventions delivered over digital devices can provide real-time encouragement for children to be physically active. Prior interventions delivered over mobile devices were effective in increasing PA levels, including our own P-Mobile study that provided behavioral strategies to parents of children aged 6 to 10 years.
When considering how to support and motivate parents whose children are preschool-aged, teaching and modeling fundamental motor skills (FMS) are critical to enable children's PA. FMS like running, jumping, or throwing a ball, are basic, goal-directed movement patterns developed in early childhood that provide a foundation for children to be physically active and competent movers. These skills enable a child to function independently in their surrounding environment, engage with peers, and contribute to their ability to be physically active. Evidence has shown that children must establish a minimal level of FMS proficiency to continue participating in PA opportunities as they age. FMS and PA behaviors have a dynamic and reciprocal relationship. Children with higher levels of FMS are more physically active both during childhood and into adolescence. Therefore, a PA intervention for preschoolers should focus on developing FMS competence.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Louisiana
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Baton Rouge, Louisiana, United States, 70808
- Pennington Biomedical Research Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 3-5 years of age
- Physically capable of exercise
- Has no parent-reported mobility limitations that impairs performance of fundamental motor skills
Exclusion Criteria:
• Gross Motor Quotient at "gifted or very advanced" based on the Test of Gross Motor Development (TGMD-3)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Fundamental Motor Skills (FMS)
The FMS group will utilize the PLAY FMS app that provides instructional lessons, peer modeling videos, and activity breaks to deliver 720 minutes of targeted, structured FMS instruction time to the child over a 12 week period.
|
Lessons will be provided over the app each week with notifications sent 5 days/week over 12 weeks specific to randomized experimental group.
|
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Active Comparator: Unstructured Physical Activity
The active comparator group will use a version of the PLAY app that provides instructional lessons to promote the equivalent dosage of unstructured physical activity for the child.
|
Lessons will be provided over the app each week with notifications sent 5 days/week over 12 weeks specific to randomized active comparator group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
App Adherence
Time Frame: From date of randomization until completion of the 12 weeks of intervention
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Adherence to the app intervention based on number of activity breaks completed over the 12 week intervention
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From date of randomization until completion of the 12 weeks of intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Test of Gross Motor Development (TGMD-3) Percentile Rank Between Baseline and Week 12
Time Frame: baseline and 12 weeks (primary outcome)
|
A validated, reliable observation assessment to evaluate fundamental motor skills performance.
Percentile ranks range from 1st (lowest) to 99th (highest/best).
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baseline and 12 weeks (primary outcome)
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Amanda Staiano, PhD, Pennington Biomedical Study Director
- Principal Investigator: E. Kipling Webster, PhD, Augusta University
Publications and helpful links
General Publications
- Webster EK, Kracht CL, Newton RL Jr, Beyl RA, Staiano AE. Intervention to Improve Preschool Children's Fundamental Motor Skills: Protocol for a Parent-Focused, Mobile App-Based Comparative Effectiveness Trial. JMIR Res Protoc. 2020 Oct 20;9(10):e19943. doi: 10.2196/19943.
- Staiano AE, Newton RL, Beyl RA, Kracht CL, Hendrick CA, Viverito M, Webster EK. mHealth Intervention for Motor Skills: A Randomized Controlled Trial. Pediatrics. 2022 May 1;149(5):e2021053362. doi: 10.1542/peds.2021-053362.
- Staiano AE, Saha S, Beyl RA, Kracht CL, Newton, Jr RL, Webster EK. Parental engagement and implementation fidelity through a mHealth motor skills intervention for young children. Physical Education and Sport Pedagogy Journal. 2023. ePub online. Doi: 10.1080/17408989.2023.2235394.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- PBRC 2018-041
- 1R21HD095035-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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