Virtual Reality During Exercise Testing

June 19, 2024 updated by: Andrew Moore, Augusta University

Effects of Virtual Reality on Cardiorespiratory Fitness Test Results

The goal of this clinical trial is to explore the effects of virtual reality use on maximal aerobic exercise test performance (aerobic capacity) in healthy adults. The main questions it aims to answer are:

  • Does using a virtual reality program during a maximal aerobic exercise test lead to differences in VO2peak (maximal aerobic capacity)? and,
  • Does using a virtual reality program during a maximal aerobic exercise test lead to differences in work rate at the ventilatory threshold?

Participants will complete a maximal aerobic exercise test two times (separated by 1 week of recovery) under the following conditions:

  • normal testing conditions in a lab
  • while viewing a virtual reality video

Researchers will compare the test results of both conditions to see if the use of a virtual reality program alters VO2peak or the ventilatory threshold.

Study Overview

Detailed Description

Virtual reality imparts a dissociative effect on users during exercise, such that the physical activity task is experienced as more enjoyable and pleasant, requires less exertion, and requires less physiological function for a given submaximal work rate.

This array of positive effects may be particularly advantageous during a maximal aerobic exercise test, mainly because participant motivation and negative psychological state often lead to premature test termination. Ameliorating the unpleasantness of this type of exercise test with the use of virtual reality technology may prolong effort expenditure during the test and result in superior performance compared to a control condition.

Additionally, improving physiological function at submaximal work rates may lead to alterations in other important testing outcomes, particularly the ventilatory threshold. The ventilatory threshold is used as a reference point for prescribing exercise intensity. An intervention that modifies this value would have repercussions for physical fitness practitioners who prescribe exercise intensity relative to the ventilatory threshold.

The general purpose of this study is to determine the effect of virtual reality on maximal aerobic exercise test performance in healthy adults. The specific questions it aims to answer are:

  • Does using a virtual reality program during a maximal aerobic exercise test lead to differences in VO2peak (maximal aerobic capacity)? and,
  • Does using a virtual reality program during a maximal aerobic exercise test lead to differences in work rate at the ventilatory threshold?

Secondary questions this study aims to answer include:

Does using a virtual reality program during a maximal aerobic exercise test lead to differences in

  • exercise test time?
  • maximal heart rate during the exercise test?
  • maximal respiratory exchange ratio (RER) during the exercise test?
  • heart rate (HR) at the ventilatory threshold?
  • RER at the ventilatory threshold?
  • psychological response [rating of perceived exertion (RPE) and affective valence] throughout the exercise test?

To address these aims, participants will complete the same maximal aerobic exercise test on a cycler ergometer under normal laboratory conditions (Control) and when viewing an immersive virtual reality video (VR). The two tests will be completed in a randomized and counterbalanced order to account for learning or familiarity effects, and will be separated by 1 week to account for the effects of testing fatigue.

Respiratory data, HR, RPE, and affective valence were collected during the exercise tests to address the aims of the study.

Study Type

Interventional

Enrollment (Estimated)

24

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Georgia
      • Augusta, Georgia, United States, 30909
        • Recruiting
        • Augusta University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

-

Exclusion Criteria:

  • Answering "YES" to one or more items on the Physical Activity Readiness Questionnaire (PAR-Q).
  • Women who are pregnant at the time of participation according to a pregnancy test.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Control condition completed first
In this arm, the Control condition (traditional maximal cardiorespiratory exercise test) will be completed first, and the Virtual Reality condition (traditional maximal cardiorespiratory exercise test with the addition of virtual reality video) will be completed second.
Participants will watch a video on a virtual reality headset during the completion of the maximal cardiorespiratory exercise test.
Participants will complete the maximal cardiorespiratory exercise test under control conditions without video, music, or other distractions.
Experimental: Virtual Reality condition completed first
In this arm, the Virtual Reality condition (traditional maximal cardiorespiratory exercise test with the addition of virtual reality video) will be completed first, and the Control condition (traditional maximal cardiorespiratory exercise test) will be completed second.
Participants will watch a video on a virtual reality headset during the completion of the maximal cardiorespiratory exercise test.
Participants will complete the maximal cardiorespiratory exercise test under control conditions without video, music, or other distractions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
VO2peak
Time Frame: Assessed during the exercise test for each condition.
The highest level of oxygen uptake averaged over a 20-second period.
Assessed during the exercise test for each condition.
Ventilatory threshold
Time Frame: Assessed during the exercise test for each condition.
The work load (in Watts) during the maximal cardiorespiratory exercise test at which breakpoints are identified between metabolic measures associated with the ventilatory threshold (CO2 production and O2 utilization; ventilatory equivalent for O2 and O2 utilization; and excess CO2 production).
Assessed during the exercise test for each condition.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Peak power
Time Frame: Assessed during the exercise test for each condition.
The work load (in Watts) of the highest exercise test stage that was completed
Assessed during the exercise test for each condition.
Total test time
Time Frame: Assessed during the exercise test for each condition.
The duration of the test (in minutes), not including the warm-up.
Assessed during the exercise test for each condition.
RPE
Time Frame: Assessed throughout the exercise test for each condition (at the end of the warm-up and end of every even-numbered stage)..
Rating of Perceived Exertion measured from 0 (no perceived exertion) to 10 (maximal perceived exertion).
Assessed throughout the exercise test for each condition (at the end of the warm-up and end of every even-numbered stage)..
Affective Valence
Time Frame: Assessed throughout the exercise test for each condition (at the end of the warm-up and end of every even-numbered stage)..
Affective valence measured from -5 (feeling very bad) to +5 (feeling very good).
Assessed throughout the exercise test for each condition (at the end of the warm-up and end of every even-numbered stage)..
%VO2peak at ventilatory threshold
Time Frame: Assessed during the exercise test for each condition.
The percentage of VO2peak at which the ventilatory threshold was reached.
Assessed during the exercise test for each condition.
Heart rate at ventilatory threshold
Time Frame: Assessed during the exercise test for each condition.
The heart rate corresponding to the time that the ventilatory threshold was reached.
Assessed during the exercise test for each condition.
Heart rate at VO2peak
Time Frame: Assessed during the exercise test for each condition.
The heart rate (in beats per minute) at which VO2peak was reached.
Assessed during the exercise test for each condition.
Respiratory Exchange Ratio (RER) at VO2peak
Time Frame: Assessed during the exercise test for each condition.
The proportion of carbon dioxide production to oxygen consumption when VO2peak was reached.
Assessed during the exercise test for each condition.
Respiratory Exchange Ratio (RER) at ventilatory threshold
Time Frame: Assessed during the exercise test for each condition.
The proportion of carbon dioxide production to oxygen consumption when the ventilatory threshold was reached.
Assessed during the exercise test for each condition.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Andrew R Moore, PhD, Augusta University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 7, 2024

Primary Completion (Estimated)

October 7, 2024

Study Completion (Estimated)

October 7, 2024

Study Registration Dates

First Submitted

June 13, 2024

First Submitted That Met QC Criteria

June 13, 2024

First Posted (Actual)

June 18, 2024

Study Record Updates

Last Update Posted (Actual)

June 21, 2024

Last Update Submitted That Met QC Criteria

June 19, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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