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Completed

NCT Number: NCT06280859

Hoosier Sport: Developing and Implementing a Sustainable Campus-Community Partnership in Rural Indiana

The clinical trial aims to develop and pilot test a multilevel physical activity (PA) intervention called the Hoosier Sport program. The study follows a participatory co-design protocol involving youth, parents, and community leaders to provide direct input into the intervention's design. The ultimate goal is to contribute to health equity in the community by promoting sustainable physical activity. Hoosier Sport involves delivering enhanced physical education classes, teaching about nutrition and exercise, as well as developing leadership skills in middle school rural students.The intervention will last for 8-weeks with PE classes occur twice a week. Additionally, Hoosier Sport will create more opportunities for students to be active at school (e.g., in home room) through providing virtual classes and other activities.

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Key information

Age range

9 year–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Indiana University

Bloomington, Indiana, 47405, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Has PE class the semester during Hoosier Sport-
  • Parent provides informed consent

Exclusion criteria

  • Answer yes to any question on the Physical Activity Readiness for Everybody (PARQ+)

Treatment and study plan

Hoosier Sport

Behavioral

Hoosier Sport is a sport-based youth development intervention. The intervention targets physical activity levels, exercise and nutrition knowledge, and leadership skills. The intervention is delivered in person twice a week (Tue/Thu) during PE class. Each class lasts 45-minutes, and covers sport skills, and then a brief lecture and activity on exercise/nutrition/leadership skills. Additionally, once a week Hoosier Sport is delivered virtually (via Zoom) during home room for 20-minutes. This involves activities to allow the students to be active during the school-day.

Primary outcomes

  1. Feasibility of Intervention Measure (FIM)

    Time frame: Measured at week 0 and week 9

    How feasible the intervention was from the perspective of the participants. This is measured through questionnaire.

  2. Acceptability of Intervention Measure (IAM)

    Time frame: Measured at week 0 and week 9

    How acceptable the intervention is to the participants. This is measured through questionnaire.

  3. Intervention Appropriateness Measure (AIM)

    Time frame: Measured at week 0 and week 9

    How appropriate the intervention is to the participants. This is measured through questionnaire.

Secondary outcomes

  1. Daily Steps of Participants

    Time frame: Week 1 (for 7 days), and week 9 (for 7 days)

    Accelerometers (Axivity - AX3 model) will be used to track daily steps

  2. Daily Moderate to Vigorous Physical Activity of Participants

    Time frame: Week 1 (for 7 days), and week 9 (for 7 days)

    Accelerometers (Axivity - AX3 model) will be used to track daily MVPA

  3. Heart Rate of Participants

    Time frame: HR will be taken at week 0 and week 9 before and following the 6-minute walk test.

    heart rate measured via a blood pressure monitor

  4. Blood Pressure of Participants

    Time frame: BP will be taken at week 0 and week 9 before and following the 6-minute walk test.

    Blood pressure measured via a blood pressure monitor

  5. Basic Psychological Needs of Participants in Intervention Environment

    Time frame: Assessed at week 0 and week 9

    Basic Psychological Needs and Satisfaction and Frustration scale (BPNSF). This entails feelings/perceptions of autonomy, relatedness, competence, enjoyment, satisfaction, and frustration in the study setting.

  6. Physical Literacy of Participants

    Time frame: Assessed at week 0 and week 9

    the Canadian Assessment of Physical Literacy second addition (CAPL-2) will be used. A higher score on the CAPL-2 indicates higher physical literacy.

  7. Cardiovascular Fitness Levels of Participants

    Time frame: Assessed at week 0 and week 9

    the 6-minute walk test will be used to assess changes in fitness. Greater distance walked in the 6 minute time frame is related to greater levels of cardiovascular fitness.

  8. Muscular Endurance Levels of Participants

    Time frame: Assessed at week 0 and week 9

    The plank test will be used to assess changes in fitness. The longer the plank is held, the greater the muscular endurance of the participant.

  9. Self-Reported Weekly Moderate to Vigorous Physical Activity of Participants

    Time frame: Assessed at week 0 and week 9

    The Canadian Assessment of Physical Literacy Second Edition (CAPL-2) will be used to assess self-reported weekly MVPA.

  10. Nutrition Knowledge of Participants

    Time frame: Assessed at week 0 and week 9

    A survey will assess basic knowledge of nutrition. We will use knowledge of SNAP-Ed, the United State Department of Agriculture's recommended curriculum. There will be three questions, with a high score reflecting greater nutrition knowledge.

  11. Policy, Systems, and Environmental Factors Influencing Participant Physical Activity and Nutrition Behavior.

    Time frame: Assessed at week 0 and week 9

    a survey will collect data on Policy, Systems and Environmental (PSE) changes using a 5 questions guided by the SNAP-Ed curriculum. Higher scores will indicate better PSE support for physical activity and healthy nutrition opportunities for the participants in their school environment.

Sponsors and collaborators

Lead sponsor

Indiana University

Other

Collaborators

  • United States Department of Agriculture (USDA)

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Feb 28, 2024
Registry last updated
Aug 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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