Actively Recruiting
Evaluating Heat Acclimation by Warm Water Immersion to Reduce Heat and Cardiovascular Stress in Older Women During Indoor Overheating
Led by University of Ottawa · Updated on 2025-06-15
12
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying ways to help older women become more resilient to heat during indoor overheating events, which are expected to increase due to global warming. The study focuses on women aged 65 to 85, who are more vulnerable to heat stress and related health risks, especially those without access to air conditioning or reliable electricity. Previous findings showed that passive heat exposure like warm-water immersion may improve the body's ability to lose heat and reduce strain, but this has not yet been confirmed in realistic indoor heat conditions for older women. Participants will undergo a 7-day heat acclimation protocol involving warm-water immersion up to shoulder level in approximately 40°C water until their core temperature reaches about 38.5°C and is maintained for 60 minutes. Before and after this protocol, they will be exposed to a 10-hour indoor heat session at 36°C and 45% humidity, simulating extreme indoor heat conditions. During this exposure, participants will mostly remain seated with brief hourly stretching breaks. During the study, researchers will monitor core body temperature, heart rate, blood pressure, cognitive function, balance, and mood among other measures to assess heat and cardiovascular strain. They will also track fluid loss, thirst, thermal comfort, and symptoms related to heat exposure. These evaluations will help determine whether the warm-water immersion protocol reduces the physical and mental stress caused by prolonged heat exposure. The total study duration includes the 7-day immersion period and assessments before and after the heat exposures.
CONDITIONS
Brief Title
Enhancing Heat Resiliency in Older Adults During Indoor Overheating Via Heat Acclimation by Warm Water Immersion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Non-smoking
- Female aged 65 to 85 years
- Able to speak English or French
- Able to provide informed consent
- May have controlled chronic hypertension or type 2 diabetes diagnosed at least 5 years ago
You will not qualify if you...
- Severe hypoglycemia episodes or inability to sense hypoglycemia
- Serious diabetes complications such as gastroparesis, kidney disease, uncontrolled hypertension, severe neuropathy
- Uncontrolled hypertension (blood pressure >150/95 mmHg sitting)
- Physical activity restrictions from diseases like unstable cardiac or pulmonary disease, severe arthritis, disabling stroke
- Use of or recent changes in medication that may affect study participation
- Cardiac abnormalities found during screening
- Current smokers or tobacco users (implied from inclusion criteria requiring non-smoking status if applicable)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo a 10-hour passive heat exposure in a climate-controlled chamber set at 36°C and 45% humidity, remaining mostly seated with hourly stretching breaks.
1 visit (in-person)
Duration - 7 days
Participants are immersed in warm water (~40°C) up to shoulder level until their core temperature reaches 38.5°C for 60 minutes. This warm-water immersion is repeated for 7 consecutive days.
7 visits (in-person, daily)
Duration - 1 day
Participants undergo a second 10-hour passive heat exposure in a climate-controlled chamber set at 36°C and 45% humidity, remaining mostly seated with hourly stretching breaks to assess the effects of acclimation.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
University of Ottawa
Ottawa, Ontario, Canada, K1N1A2
Actively Recruiting
Research Team
G
Glen P Kenny, PhD
C
Caroline Li-Maloney, MSc
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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