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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06464406
Other study ID # 2130870
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 7, 2024
Est. completion date October 7, 2024

Study information

Verified date June 2024
Source Augusta University
Contact Andrew R Moore, PhD
Phone 650-477-7746
Email andmoore@augusta.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Recruiting
Enrollment 24
Est. completion date October 7, 2024
Est. primary completion date October 7, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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


Related Conditions & MeSH terms


Intervention

Behavioral:
Virtual Reality condition
Participants will watch a video on a virtual reality headset during the completion of the maximal cardiorespiratory exercise test.
Control condition
Participants will complete the maximal cardiorespiratory exercise test under control conditions without video, music, or other distractions.

Locations

Country Name City State
United States Augusta University Augusta Georgia

Sponsors (1)

Lead Sponsor Collaborator
Augusta University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary VO2peak The highest level of oxygen uptake averaged over a 20-second period. Assessed during the exercise test for each condition.
Primary Ventilatory threshold 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 Peak power The work load (in Watts) of the highest exercise test stage that was completed Assessed during the exercise test for each condition.
Secondary Total test time The duration of the test (in minutes), not including the warm-up. Assessed during the exercise test for each condition.
Secondary RPE 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)..
Secondary Affective Valence 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)..
Secondary %VO2peak at ventilatory threshold The percentage of VO2peak at which the ventilatory threshold was reached. Assessed during the exercise test for each condition.
Secondary Heart rate at ventilatory threshold The heart rate corresponding to the time that the ventilatory threshold was reached. Assessed during the exercise test for each condition.
Secondary Heart rate at VO2peak The heart rate (in beats per minute) at which VO2peak was reached. Assessed during the exercise test for each condition.
Secondary Respiratory Exchange Ratio (RER) at VO2peak The proportion of carbon dioxide production to oxygen consumption when VO2peak was reached. Assessed during the exercise test for each condition.
Secondary Respiratory Exchange Ratio (RER) at ventilatory threshold The proportion of carbon dioxide production to oxygen consumption when the ventilatory threshold was reached. Assessed during the exercise test for each condition.
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