N/A
N=10
"Facemask Use During High-intensity Interval Exercise in Temperate and Hot Environments"
Hypoxemia · Physiological Stress
Bottom Line
View on ClinicalTrials.gov: NCT05143801 ↗Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Apr 2022
Primary outcome: Primary: Average Heart Rate Over the Course of High-intensity Interval Exercise — 144; 143; 148; 149 beats per minute — p=0.003
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- High-intensity interval exercise with surgical face mask in a temperate environment (Device); High-intensity interval exercise with surgical face mask in a hot environment (Device); High-intensity interval exercise without using a surgical face mask in a hot environment (Other); High-intensity interval exercise without using a surgical face mask in a temperate environment (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of New Mexico
- Primary completion
- Jun 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Average Heart Rate Over the Course of High-intensity Interval Exercise |
144; 143; 148; 149 | 0.003 sig |
| PRIMARY Average Stroke Volume Over the Course of High-intensity Interval Exercise |
109.9; 109.2; 104.5; 101.5 | 0.117 |
| PRIMARY Average Cardiac Output Over the Course of High-intensity Interval Exercise |
15.7; 15.8; 15.3; 16.5 | 0.749 |
| PRIMARY Peak Core Temperature |
37.76; 37.64; 37.65; 37.71 | 0.789 |
| PRIMARY Change From Baseline (Rest) in Core Temperature to the End of Exercise |
0.77; 0.54; 0.56; 0.64 | 0.394 |
| PRIMARY Sweat Rate During Exercise |
2097; 1921; 2262; 1793 | 0.960 |
| PRIMARY Dehydration After Exercise |
-0.76; -0.77; -0.81; -0.67 | 0.786 |
| PRIMARY Lactate at 5-minutes Post Exercise |
4.3; 4.2; 4.9; 4.5 | 0.134 |
| PRIMARY Average Blood Oxygen Saturation Over the Course of High-intensity Interval Exercise |
93.5; 93.7; 93.8; 94.0 | 0.461 |
| PRIMARY Average Muscle Tissue Oxygenation During the High-intensity Portions of the Exercise Session |
31.0; 31.4; 23.5; 34.7 | 0.466 |
| PRIMARY Average Muscle Tissue Oxygenation During the Active Rest Portions of the Exercise Session |
56.7; 58.8; 55.8; 62.0 | 0.375 |
| PRIMARY Average Change in Muscle Tissue Oxygenation Between the Active Rest and High Intensity Portions Over the Course of High-intensity Interval Exercise. |
25.6; 27.5; 32.4; 27.4 | 0.290 |
| PRIMARY Average Perceived Dyspnea Score Over the Course of High-intensity Interval Exercise |
14; 44; 18; 58 | 0.018 sig |
| PRIMARY Peak Thermal Sensation Over the Course of High-intensity Interval Exercise |
5.9; 5.9; 6.5; 6.6 | <0.001 sig |
| PRIMARY Average Thermal Sensation Over the Course of High-intensity Interval Exercise |
5.3; 5.4; 6.5; 6.6 | <0.001 sig |
| PRIMARY Peak Rating of Perceived Exertion Over the Course of High-intensity Interval Exercise |
15; 15; 15; 16 | 0.089 |
| PRIMARY Averaged Rating of Perceived Exertion Over the Course of High-intensity Interval Exercise |
13.3; 13.3; 13.5; 14.3 | 0.024 sig |
| PRIMARY Peak Heart Rate Over the Course of High-intensity Interval Exercise |
164; 164; 169; 169 | 0.012 sig |
Summary
To investigate surgical mask use and high-intensity interval exercise across different environmental conditions.
Eligibility Criteria
Inclusion Criteria
- 18 years of age or older and, are able to both speak and read in English.
- Physically active and used to high-intensity exercise.
- No known serious medical conditions.
Exclusion Criteria
- Vulnerable populations such as children, minors, pregnant women, and intellectually challenged individuals.
- Those with cardiovascular, renal, metabolic, or chronic respiratory disease, smokers or those who have quit smoking less than 6 months ago, and those who use an inhaler to control for exercise-induced asthma.
- In addition, exclusion criteria include participants who show any signs or symptoms of COVID-19 and have had exposure to anyone with COVID-19 symptoms or any person that has tested positive for COVID-19.
Data sourced from ClinicalTrials.gov (NCT05143801). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.