YouTube-Delivered Physical Activity Intervention

Sponsor
University of Minnesota (Other)
Overall Status
Completed
CT.gov ID
NCT04499547
Collaborator
(none)
64
1
2
4.8
13.3

Study Details

Study Description

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).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: YouTube-delivered aerobic and muscle-strengthening physical activity intervention
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Effect of a YouTube-Delivered Physical Activity Intervention on College Students' Aerobic and Muscle-Strengthening Physical Activity: A Randomized Controlled Trial
Actual Study Start Date :
Dec 2, 2020
Actual Primary Completion Date :
Mar 27, 2021
Actual Study Completion Date :
Apr 28, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Physical activity intervention

Will receive twice-weekly, YouTube-delivered aerobic and muscle-strengthening physical activity videos for 8 weeks.

Behavioral: YouTube-delivered aerobic and muscle-strengthening physical activity intervention
Participants in the intervention group will receive two YouTube-delivered videos each week, for 8 weeks. In detail, on Monday, participants will receive an aerobic-based physical activity video with information and a workout to complete and on Thursdays, the participants will receive a video with muscle-strengthening physical activity information and a workout to complete.

No Intervention: General health education control

Will receive twice-weekly, YouTube-delivered videos with general health education information for 8 weeks.

Outcome Measures

Primary Outcome Measures

  1. 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

  2. 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.

Secondary Outcome Measures

  1. Change in sleep quality [Baseline, 4 weeks (mid), and 8 weeks (end)]

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

  2. Change in cardiorespiratory Fitness [Baseline, 4 weeks (mid), and 8 weeks (end)]

    YMCA 3-minute step test

  3. Change in muscular fitness [Baseline, 4 weeks (mid), and 8 weeks (end)]

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

  4. Change in intrinsic Motivation [Baseline, 4 weeks (mid), and 8 weeks (end)]

    Psychosocial survey

  5. Change in social support [Baseline, 4 weeks (mid), and 8 weeks (end)]

    Psychosocial survey

  6. Change in perceived physical activity barriers [Baseline, 4 weeks (mid), and 8 weeks (end)]

    Psychosocial survey

  7. Change in body weight (kg) [Baseline, 4 weeks (mid), and 8 weeks (end)]

    Measured using stadiometer to the nearest 0.1 kg

  8. Height (cm [Baseline]

    Measured using digital bodyweight scale to the nearest 0.1 cm

  9. 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Minnesota - Twin Cities Minneapolis Minnesota United States 55455

Sponsors and Collaborators

  • University of Minnesota

Investigators

  • Principal Investigator: Daniel J McDonough, M.S., University of Minnesota

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Minnesota
ClinicalTrials.gov Identifier:
NCT04499547
Other Study ID Numbers:
  • 2728
First Posted:
Aug 5, 2020
Last Update Posted:
Apr 6, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Minnesota

Study Results

No Results Posted as of Apr 6, 2022