- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06902727
Effects of Virtual Reality Exercise on Promoting Physical Activity and Health Among College Students
Effects of Virtual Reality Exercise on Promoting Physical Activity and Health Among College Students: A 4-week Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Minnesota
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Minneapolis, Minnesota, United States, 55455
- University of Minnesota, Twin Cities
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- College students age from 18 to 35 years old who are currently enrolled in the university
- College students without diagnosed physical and/or mental disabilities
- Must be willing to provide informed consent and compete the PA Readiness Questionnaire (PAR-Q)
- Must be willing to be randomized into an intervention or control group
- no self-reported motion sickness symptoms during immersive VR-based exercise
Exclusion Criteria:
- Students under the age of 18 or over the age of 35 years old or not currently enrolled in the university
- Having self-reported physical and/or mental disabilities
- Contradictions to PA participation as determined by PAR-Q responses
- having motion sickness reaction when exercising under VR-based condition.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Exercise on immersive VR-based bike
Participants were asked to exercise on an immersive VR-based exercise bike for one hour per session, two times per week, for 4 weeks
|
For the intervention group, participations exercised on an immersive VR-based exercise bike for one hour, twice per week, for 4 weeks.
Participants in the control group were asked to maintain their usual routine after the baseline test for 4 weeks.
Participants were scheduled separately coming to lab for the post-test after 4 weeks and all participants received the identical assessments in aforementioned physiological and psychological outcomes.
|
|
Active Comparator: Usual routine
Participants in the control group were asked to maintain their usual routine after the baseline test for 4 weeks.
Participants were scheduled separately coming to lab for the post-test after 4 weeks and all participants received the identical assessments in aforementioned physiological and psychological outcomes.
|
Participants were asked to maintain their usual activities, without engaging in any other physical activity intervention during the 4-week study period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exercise Motivation
Time Frame: Baseline, and 4 weeks
|
Participants' motivation were assessed by the Behavioral Regulation in Exercise Questionnire-2 (BREQ-2).
The BREQ-2 has 19 items assessing the continuum of behavioral regulation in exercise, which included amotivation, external regulation, introjected regulation, identified regulation, and intrinsic regulation.
|
Baseline, and 4 weeks
|
|
Mood States
Time Frame: Baseline, and 4 weeks
|
Participants' mood states were measured by the Brunel Mood Scale (BRUMS).
The BRUMS assesses mood across six subscales (anger, confusion, depression, fatigue, tension, and vigor) using a 24-item questionnaire with responses ranging from 0 (not at all) to 4 (extremely).
|
Baseline, and 4 weeks
|
|
Depressive Symptoms
Time Frame: Baseline, and 4 weeks
|
The Beck Depression Inventory (BDI) was used to assess participant's depressive symptoms.
This is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression.
The total score was calculated to the evaluate the severity of depressive symptoms.
|
Baseline, and 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cardiovascular fitness levels
Time Frame: Baseline, and 4 weeks
|
Investigators asked participants to step on and off of a 12-inch plyometric box for 3 minutes to the "beep" of a metronome set to 96 beats-per-minute, with each beep corresponding with one leg movement.
Immediately following the completion of the test, the principal investigator measured participants' heart rate for 60 seconds via palpation of the radial artery on the underbelly of the left wrist.
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Baseline, and 4 weeks
|
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Physical activity levels
Time Frame: Baseline, and 4 weeks
|
Physical activity levels were assessed via International Physical Activity Questionnaire (IPAQ). The IPAQ assesses three specific types of activity: walking, moderate-intensity activities, and vigorous-intensity activities. It asks participants to recall the time (in minutes) spent on each of these activities in the past 7 days. Each participant were assigned an accelerometer to wear during each 60-minute exercise session. Prior to the start of the intervention, participants were asked to wear an accelerometer for one week for measuring their physical activity levels. In addition, the investigators asked participants to wear the accelerometer for another week at the completion of 4-week intervention. |
Baseline, and 4 weeks
|
|
Body Mass Index
Time Frame: Baseline, and 4 weeks
|
Participant height (cm) and weight (kg) were measured using a stadiometer and a Tanita BC-558 IRONMAN Segmental Body Composition Monitor, respectively, in theUniversity of Minnesota's Physical Activity Epidemiology Laboratory.
Both height and weight were used to calculate BMI in kg/m².
BMI was classified according to the following indicators: Underweight: BMI < 18.5; Normal weight: BMI 18.5-24.9;
Overweight: BMI 25-29.9;
Obesity: BMI ≥ 30.
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Baseline, and 4 weeks
|
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Percent of body fat
Time Frame: Baseline, and 4 weeks
|
Percent of body fat (%BF) were measured by Tanita BC-558 IRONMAN Segmental Body Composition Monitor.
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Baseline, and 4 weeks
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Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00010580
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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