Actively Recruiting

Phase Not Applicable
Age: 65Years - 85Years
FEMALE
Healthy Volunteers
ID07032493

Identifying the Upper Environmental Limits of Thermal Compensation in Older Human Females Using a Rapid Humidity Ramp Protocol

Led by University of Ottawa · Updated on 2025-11-28

12

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how extreme heat affects older females aged 65 to 85 years, focusing on their ability to lose heat compared to males. This study aims to understand when heat stress becomes too great for their bodies to handle, known as the limit of compensability, and how this relates to risks of heat-related illness. The research will assess physical, psychological, and cognitive responses to different heat conditions using a ramping protocol and fixed heat exposures. Participants will undergo five trials, starting with a humidity-ramp protocol where they rest in warm conditions (42°C, 28% humidity) and then experience gradual increases in humidity until a critical point is reached. Subsequent trials expose participants to fixed humidity levels set around this critical point, including levels below, above, and a control thermo-neutral condition. Each fixed exposure lasts up to 9 hours with water provided to reduce dehydration risk. The order of the fixed exposures is randomized after completing the ramping protocol. During the study, researchers will monitor core temperature changes, heart rate, sweat rate, thermal comfort, mood, and environmental symptoms. They will track how quickly body temperature rises and measure cumulative strain under different heat conditions. The study also evaluates how many participants can complete each exposure and assesses psychological and cognitive effects. Participation involves repeated visits over the study period, with continuous monitoring to understand heat tolerance in older females better.

CONDITIONS

Brief Title

Identifying the Limits of Survivability in Heat-exposed Older Females

Who Can Participate

Age: 65Years - 85Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female aged between 65 and 85 years
  • Non-smoking
  • English or French speaking
  • Ability to provide informed consent
  • With or without chronic hypertension or type 2 diabetes diagnosed at least 5 years ago
Not Eligible

You will not qualify if you...

  • Severe hypoglycemia episodes requiring assistance within the past year or inability to sense hypoglycemia
  • Serious diabetes complications such as gastroparesis, renal disease, uncontrolled hypertension, or severe autonomic neuropathy
  • Uncontrolled hypertension with blood pressure over 150/95 mmHg while sitting
  • Physical activity restrictions due to diseases like intermittent claudication, renal impairment, severe arthritis, unstable cardiac or pulmonary disease, disabling stroke
  • Use of or changes in medication making participation inadvisable
  • Cardiac abnormalities found during screening

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Humidity-Ramp Protocol

Duration - Approximately 1.5 hours per session

Participants are exposed to a controlled heat and humidity environment where humidity is gradually increased to determine their individual thermal response limits.

1 visit (in-person)

Fixed-Condition Heat Exposures

Duration - Up to 9 hours per session; multiple sessions in randomized order

Participants complete multiple randomized heat exposure sessions at fixed humidity levels set relative to their individual thermal limits determined from the humidity-ramp protocol. Each exposure lasts up to 9 hours with breaks for hydration.

Multiple visits (in-person) depending on randomized schedule

Trial Site Locations

Total: 2 locations

1

University of Ottawa

Ottawa, Ontario, Canada, K1N6N5

Not Yet Recruiting

2

University of Ottawa

Ottawa, Ontario, Canada

Actively Recruiting

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Research Team

G

Glen P Kenny, PhD

C

Caroline Li-Maloney, MSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

5

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