YouTube-Delivered Physical Activity Intervention
- Conditions
- Healthy
- Interventions
- Behavioral: YouTube-delivered aerobic and muscle-strengthening physical activity intervention
- Registration Number
- NCT04499547
- Lead Sponsor
- University of Minnesota
- Brief Summary
This study will be an 8-week randomized controlled trial examining the effects of a YouTube-delivered aerobic and muscle strengthening physical activity intervention on university students' physical activity, fitness, sleep quality, and psychosocial health outcomes. Participants will be randomized into 1 of 2 groups: (1) intervention group (receive twice-weekly YouTube videos \[1 aerobic workout video; 1 muscle-strengthening workout video\] for 8 weeks); or (2) control group (receive twice-weekly YouTube videos with general health information \[no physical activity-related information or workouts\] for 8 weeks). Baseline (0 weeks), mid-point (4 weeks), and post-test (8 weeks) testing will take place and the following outcome measures will be assessed at these time points: participants' free-living (7-day) objectively-measured physical activity and sleep quality data will be collected; anthropometric measures (height, weight, percent body fat); cardiorespiratory and muscular fitness; and psychosocial assessments (perceived physical activity barriers and social support).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 64
- 18-35 years of age; able to participate in aerobic and muscle-strengthening exercise; healthy (i.e., no diseases or clinical/mental health conditions which will prevent physical activity participation); does not meet minimum physical activity guidelines criteria for aerobic (≥ 150 minutes per week of moderate-to-vigorous intensity physical activity) and muscle-strengthening (≥ 2 days per week; 8-10 exercises for all major muscle groups) physical activity at time of enrollment; willing to be randomized to the intervention or control group.
- less than 18 years old or greater than 35 years old; physical or mental health contradictions which do not allow participants to participate in physical activity; exceed minimum aerobic or muscle-strengthening physical activity guideline recommendations; unwilling to be randomized to either intervention or control group.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Physical activity intervention YouTube-delivered aerobic and muscle-strengthening physical activity intervention Will receive twice-weekly, YouTube-delivered aerobic and muscle-strengthening physical activity videos for 8 weeks.
- Primary Outcome Measures
Name Time Method Change in adherence to muscle-strengthening guidelines Baseline, 4 weeks (mid), and 8 weeks (end) Assessed by 7-day physical activity recall interview to see if participants engaged in muscle-strengthening activity at least 2 days per week.
Change in objectively measured free-living physical activity Baseline, 4 weeks (mid), and 8 weeks (end) 7-day measurement using wrist-worn ActiGraph tri-axial accelerometer
- Secondary Outcome Measures
Name Time Method Change in perceived physical activity barriers Baseline, 4 weeks (mid), and 8 weeks (end) Psychosocial survey
Change in body fat percentage Baseline, 4 weeks (mid), and 8 weeks (end) Measured using the digital weight scale used to assess body weight via bioelectrical impedance
Change in cardiorespiratory Fitness Baseline, 4 weeks (mid), and 8 weeks (end) YMCA 3-minute step test
Change in muscular fitness Baseline, 4 weeks (mid), and 8 weeks (end) 60 second pushups and sit-ups muscular endurance tests (maximal repetitions)
Change in intrinsic Motivation Baseline, 4 weeks (mid), and 8 weeks (end) Psychosocial survey
Change in body weight (kg) Baseline, 4 weeks (mid), and 8 weeks (end) Measured using stadiometer to the nearest 0.1 kg
Change in sleep quality Baseline, 4 weeks (mid), and 8 weeks (end) 7-day measurement using wrist-worn ActiGraph tri-axial accelerometer
Change in social support Baseline, 4 weeks (mid), and 8 weeks (end) Psychosocial survey
Height (cm Baseline Measured using digital bodyweight scale to the nearest 0.1 cm
Trial Locations
- Locations (1)
University of Minnesota - Twin Cities
🇺🇸Minneapolis, Minnesota, United States