MedPath

Virtual Reality During Exercise Testing

Not Applicable
Recruiting
Conditions
Virtual Reality
Interventions
Behavioral: Virtual Reality condition
Behavioral: Control condition
Registration Number
NCT06464406
Lead Sponsor
Augusta University
Brief Summary

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.

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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
24
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 & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Control condition completed firstControl conditionIn 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.
Control condition completed firstVirtual Reality conditionIn 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.
Virtual Reality condition completed firstVirtual Reality conditionIn 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.
Virtual Reality condition completed firstControl conditionIn 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.
Primary Outcome Measures
NameTimeMethod
VO2peakAssessed during the exercise test for each condition.

The highest level of oxygen uptake averaged over a 20-second period.

Ventilatory thresholdAssessed 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).

Secondary Outcome Measures
NameTimeMethod
RPEAssessed 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).

Heart rate at ventilatory thresholdAssessed during the exercise test for each condition.

The heart rate corresponding to the time that the ventilatory threshold was reached.

Peak powerAssessed during the exercise test for each condition.

The work load (in Watts) of the highest exercise test stage that was completed

Affective ValenceAssessed 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).

Heart rate at VO2peakAssessed during the exercise test for each condition.

The heart rate (in beats per minute) at which VO2peak was reached.

Respiratory Exchange Ratio (RER) at VO2peakAssessed during the exercise test for each condition.

The proportion of carbon dioxide production to oxygen consumption when VO2peak was reached.

Respiratory Exchange Ratio (RER) at ventilatory thresholdAssessed during the exercise test for each condition.

The proportion of carbon dioxide production to oxygen consumption when the ventilatory threshold was reached.

Total test timeAssessed during the exercise test for each condition.

The duration of the test (in minutes), not including the warm-up.

%VO2peak at ventilatory thresholdAssessed during the exercise test for each condition.

The percentage of VO2peak at which the ventilatory threshold was reached.

Trial Locations

Locations (1)

Augusta University

🇺🇸

Augusta, Georgia, United States

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