Effect of Pre-cooling on Whole-body Heat Loss During Exercise-heat Stress
NCT ID: NCT06670339
Last Updated: 2025-06-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2024-10-24
2025-02-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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No Cooling
Participants will complete 60 min of continuous semi-recumbent cycling at a fixed metabolic heat load (200 W/m2) in the heat (wet-bulb globe temperature of 29°C; 37.5°C and 35% relative humidity) (Control condition) without pre-cooling.
No Cooling
Participants will not be pre-cooled prior to completing a 60-minute moderate-intensity exercise bout in the heat.
Pre-Cooling
Participants will undergo a cold-water immersion (\~17°C) to elicit a decrease in rectal temperature by 0.5°C from baseline values. Thereafter, once the target temperature is achieved, participants will complete 60 min of continuous moderate-intensity cycling (200 W/m2) in the heat (wet-bulb globe temperature of 29°C; 37.5°C and 35% relative humidity).
Pre-Cooling
Participants will be immersed in cold (\~17°C) water to elicit a decrease in rectal temperature by 0.5°C from baseline values prior to completing a 60-min moderate-intensity exercise bout in the heat.
Interventions
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No Cooling
Participants will not be pre-cooled prior to completing a 60-minute moderate-intensity exercise bout in the heat.
Pre-Cooling
Participants will be immersed in cold (\~17°C) water to elicit a decrease in rectal temperature by 0.5°C from baseline values prior to completing a 60-min moderate-intensity exercise bout in the heat.
Eligibility Criteria
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Inclusion Criteria
* Non-smoking
* English or French speaking
* Ability to provide informed consent
Exclusion Criteria
* Acute illness (e.g., flu, COVID-19)
* Physical restriction limiting physical activity
* Use of medication judged by the patient or investigators to make participation in this study inadvisable.
* Sedentary
18 Years
30 Years
MALE
Yes
Sponsors
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University of Ottawa
OTHER
Responsible Party
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Glen P. Kenny
Professor
Principal Investigators
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Glen P Kenny, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Ottawa
Locations
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University of Ottawa
Ottawa, Ontario, Canada
Countries
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Other Identifiers
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HEPRU-2024-08-B
Identifier Type: -
Identifier Source: org_study_id
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