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CompletedNCT04499547Updated Apr 6, 2022

YouTube-Delivered Physical Activity Intervention

An interventional study of YouTube-delivered aerobic and muscle-strengthening physical activity intervention in Healthy, sponsored by University of Minnesota. Completed at 1 site in United States. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-04-06.

Sponsored by University of Minnesota · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
64
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study 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).

02

Conditions studied

  • Healthy

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Keywords

  • youtube
  • physical activity
  • fitness
03

In context

Motor Activity

2,646 studies on the registry are indexed under Motor Activity; 1,205 are open to participants now.

This study's enrollment of 64 is close to the median of 60 across 2,309 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

University of Minnesota is the lead sponsor of 1,210 studies on the registry; 194 are open to participants now.

Of its 133 completed or terminated interventional studies of FDA-regulated products, 92 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
64 participants (actual)

Study arms

  • 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

  • No intervention
    General health education control

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

Interventions

  • BehavioralYouTube-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.

06

What researchers measure

Primary outcomes

  1. Change in objectively measured free-living physical activity

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

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  2. Change in adherence to muscle-strengthening guidelines

    Assessed by 7-day physical activity recall interview to see if participants engaged in muscle-strengthening activity at least 2 days per week.

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

Secondary outcomes

  1. Change in sleep quality

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

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  2. Change in cardiorespiratory Fitness

    YMCA 3-minute step test

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  3. Change in muscular fitness

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

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  4. Change in intrinsic Motivation

    Psychosocial survey

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  5. Change in social support

    Psychosocial survey

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  6. Change in perceived physical activity barriers

    Psychosocial survey

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  7. Change in body weight (kg)

    Measured using stadiometer to the nearest 0.1 kg

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

  8. Height (cm

    Measured using digital bodyweight scale to the nearest 0.1 cm

    Time frame: Baseline

  9. Change in body fat percentage

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

    Time frame: Baseline, 4 weeks (mid), and 8 weeks (end)

07

Study locations

1 site
  • University of Minnesota - Twin Cities
    Minneapolis, Minnesota 55455, United States
08

References and documents

Publications

  • McDonough DJ, Helgeson MA, Liu W, Gao Z. Effects of a remote, YouTube-delivered exercise intervention on young adults' physical activity, sedentary behavior, and sleep during the COVID-19 pandemic: Randomized controlled trial. J Sport Health Sci. 2022 Mar;11(2):145-156. doi: 10.1016/j.jshs.2021.07.009. Epub 2021 Jul 24. PubMed 34314877 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Dec 2020 to primary completion in Mar 2021, 3 months.

Of 1,726 non-industry interventional studies with no phase under Motor Activity, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 47. This study's 3 months is below that.

Counting every sponsor, half of 1,738 studies reached it within 23 months; a quarter within 9 and three quarters within 47.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 28, 2020
First posted
Aug 5, 2020
StartActual
Dec 2, 2020
Primary completionActual
Mar 27, 2021
CompletionActual
Apr 28, 2021
Last update
Apr 6, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 6, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04499547
Responsible party
Sponsor
First posted
Aug 5, 2020
Start date
Dec 2, 2020
Primary completion
Mar 27, 2021
Completion
Apr 28, 2021
Last update
Apr 6, 2022

Study contacts

Daniel J McDonough, M.S.
principal investigator · University of Minnesota

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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