MedPath

YouTube-Delivered Physical Activity Intervention

Not Applicable
Completed
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
Inclusion Criteria
  • 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.
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Exclusion Criteria
  • 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.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Physical activity interventionYouTube-delivered aerobic and muscle-strengthening physical activity interventionWill receive twice-weekly, YouTube-delivered aerobic and muscle-strengthening physical activity videos for 8 weeks.
Primary Outcome Measures
NameTimeMethod
Change in adherence to muscle-strengthening guidelinesBaseline, 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 activityBaseline, 4 weeks (mid), and 8 weeks (end)

7-day measurement using wrist-worn ActiGraph tri-axial accelerometer

Secondary Outcome Measures
NameTimeMethod
Change in perceived physical activity barriersBaseline, 4 weeks (mid), and 8 weeks (end)

Psychosocial survey

Change in body fat percentageBaseline, 4 weeks (mid), and 8 weeks (end)

Measured using the digital weight scale used to assess body weight via bioelectrical impedance

Change in cardiorespiratory FitnessBaseline, 4 weeks (mid), and 8 weeks (end)

YMCA 3-minute step test

Change in muscular fitnessBaseline, 4 weeks (mid), and 8 weeks (end)

60 second pushups and sit-ups muscular endurance tests (maximal repetitions)

Change in intrinsic MotivationBaseline, 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 qualityBaseline, 4 weeks (mid), and 8 weeks (end)

7-day measurement using wrist-worn ActiGraph tri-axial accelerometer

Change in social supportBaseline, 4 weeks (mid), and 8 weeks (end)

Psychosocial survey

Height (cmBaseline

Measured using digital bodyweight scale to the nearest 0.1 cm

Trial Locations

Locations (1)

University of Minnesota - Twin Cities

🇺🇸

Minneapolis, Minnesota, United States

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