- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06229457
Development and Testing of a Sports Intervention to Promote Physical Activity in Rural Girls (GirlsPLAY)
Development and Feasibility Testing of a Boys & Girls Clubs' Sports Intervention to Promote Physical Activity in Rural Girls: Girls PLAY
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Fewer than 30% of elementary-aged youth meet physical activity guidelines, with lower activity levels found among girls, racial minorities, and those living in rural areas. Sport is one of the best strategies for promoting physical activity, yet girls, Hispanics, and rural populations participate in youth sport at lower numbers and drop out at a higher rate. In line with Self-Determination Theory, commonly cited barriers include lack of competence, autonomy, and relatedness. Physical literacy and sport sampling have also been identified as key determinants of youth sport participation. Developing interventions around physical literacy and sport sampling, with intervention delivery grounded in Self-Determination Theory principles, is a promising strategy for promoting youth sport. However, the few existing interventions aimed to promote girls' physical activity through sport were developed outside the United States, focused on adolescent (versus younger) girls, and/or conducted among urban or suburban youth, limiting generalizability. Rural, Hispanic girls face unique challenges around sport that should be identified and addressed, yet there remains a paucity of information on determinants of sport participation among this population.
This study aims to to develop, tailor, and examine the impact of a tailored Boys & Girls Clubs (BGC) sport sampling and physical literacy program on rural girls' physical activity levels. BGC is an organization that provides learning and leadership programs to millions of rural youth nationwide, about half of whom are girls.
This study will enroll Hispanic girls ages 8-10 living in rural Imperial County, California. The first aims are to develop and refine a 12-week sport sampling and physical literacy intervention entitled "Girls Positive Learning Activities for Youth", or "Girls PLAY". The Girls PLAY intervention will be delivered as Boys & Girls Clubs programming, and intervention delivery will be grounded in Self-Determination Theory. We will then examine the feasibility of the 12-week Girls PLAY intervention. Secondary outcomes of physical activity levels, physical literacy, Self-Determination Theory constructs, and sports participation will also be assessed.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
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San Diego, California, United States, 92182
- San Diego State University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- living in Imperial County, California
- identify as female
- aged 8-10 years old
- enrolled at a participating Boys & Girls Club site
Exclusion Criteria:
- has a sibling enrolled in the study
- physical or mental impairment that would preclude physical activity or protocol compliance
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Girls PLAY program
|
Girls PLAY program (8-12 weeks) will include 1) a series of in-person sessions, led by Boys and Girls Clubs staff at the Boys and Girls Club sites, and 2) take-home activities.
In-person sessions (60-75 min; 2-3x/week) will center around a different developmentally appropriate sport each week.
Lesson plans will outline games/activities in which youth engage in fundamental, sport-specific movement skills.
Lesson plans will be delivered by Boys and Girls Club leaders using acts of instruction derived from Self-Determination Theory.
Take home activities will 1) summarize and add on to the week's in-person sessions and 2) be adapted for delivery by parents and/or self-guided participation by youth.
Take-home activities will provide information for engaging in the past week's activities as well as additional activities that parents and youth can participate in together.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Recruitment capability
Time Frame: Weeks 10-12
|
Feasibility metric: successfully enroll 30 participants
|
Weeks 10-12
|
|
Study assessments completed
Time Frame: Weeks 10-12
|
Feasibility metric: ≥75% participants complete time 1 and time 2 assessments
|
Weeks 10-12
|
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Intervention acceptability and appropriateness
Time Frame: Weeks 10-12
|
Feasibility metric: Mean score ≥3 on the Acceptability of Intervention Measure; mean score ≥3 on the Intervention Appropriateness Measure
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Weeks 10-12
|
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Intervention feasibility and participant attendance
Time Frame: Weeks 10-12
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Feasibility metric: Mean score ≥3 on the Feasibility of Intervention Measure
|
Weeks 10-12
|
|
Participant attendance
Time Frame: Weeks 10-12
|
Attend ≥75% of in-person sessions (on average)
|
Weeks 10-12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in physical activity levels at 10-12 weeks measured via Actigraph GT3X+
Time Frame: Week 0-1; Week 10-12
|
We will use Actigraph GT3X+ (ActiGraph LLC, Pensacola, FL) to obtain a valid, objective measure of physical activity.
Data will be collected over 7 days (sample frequency of 30 Hz; 15-sec epochs).
|
Week 0-1; Week 10-12
|
|
Change from baseline in physical literacy at 10-12 weeks measured via the Canadian Assessment for Physical Literacy, Second Edition (CAPL-2)
Time Frame: Week 0-1; Week 10-12
|
Physical literacy changes will be assessed using the Canadian Assessment for Physical Literacy, Second Edition (CAPL-2).
This includes the plank, Progressive Aerobic Cardiovascular Endurance Run, Canadian Agility & Movement Skill Assessment, and 22-item questionnaire.
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Week 0-1; Week 10-12
|
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Change from baseline in autonomy at 10-12 weeks
Time Frame: Week 0-1; Week 10-12
|
Autonomy will be measured using the 9-item Autonomy-Supportive Coaching Questionnaire.
|
Week 0-1; Week 10-12
|
|
Change in sport engagement at 10-12 weeks
Time Frame: Week 0-1; Week 10-12
|
Engagement will be assessed via child survey examining current sport involvement (length of involvement, primary and secondary sport) and behavioral intention (e.g., "I intend to play sports this year") adapted from items used in studies among similar age groups.
|
Week 0-1; Week 10-12
|
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Change in sport enjoyment at 10-12 weeks
Time Frame: Week 0-1; Week 10-12
|
Enjoyment will be assessed using an adapted 5-item Enjoyment subscale of the Sport Commitment Questionnaire-2.
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Week 0-1; Week 10-12
|
|
Change from baseline in competence at 10-12 weeks
Time Frame: Week 0-1; Week 10-12
|
Competence will be measured using an adapted version of the Perceived Competence Scale (4-item).
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Week 0-1; Week 10-12
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Change from baseline in relatedness at 10-12 weeks
Time Frame: Week 0-1; Week 10-12
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Relatedness will be measured using a 5-item acceptance subscale of the Need for Relatedness Scale.
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Week 0-1; Week 10-12
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- HS-2023-0186
- 1K01HL171860-01 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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