Actively Recruiting

Phase Not Applicable
Age: 60Years - 85Years
All Genders
Healthy Volunteers
ID06842953

Is an Adjustment in the Recommended Indoor Temperature Upper Limit of 26°C Required During Higher Levels of Humidity?

Led by University of Ottawa · Updated on 2025-06-15

10

Participants Needed

1

Research Sites

22 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how indoor humidity affects physical stress, especially in older adults aged 65 to 85 years, during heat exposure. The study focuses on whether the current recommended indoor temperature limit of 26°C needs adjustment when humidity levels change, as higher humidity may worsen heat stress by reducing sweat evaporation. This is important because climate change is increasing both temperature and humidity, which could increase health risks for vulnerable people. Participants will experience four different indoor conditions on separate occasions: 26°C at 45% humidity, 26°C at 15% humidity, 26°C at 85% humidity, and 31°C at 45% humidity. Each session lasts 10 hours, simulating a daylong heat exposure. By comparing similar perceived temperatures (humidex), investigators aim to understand how both temperature and humidity affect the body’s response to heat. During the study, researchers will measure core body temperature, heart rate, blood pressure, balance, cognitive function, mood, thirst, and fluid loss before and after exposure. They will use various scales and tests to assess physical and mental effects of heat and humidity. The study uses a randomized design with single masking and will monitor participants throughout the 10-hour exposure periods to gather detailed information on heat strain and comfort.

CONDITIONS

Brief Title

Influence of Indoor Humidity on Physiological Strain in Older Adults During a Simulated Heat Wave

Who Can Participate

Age: 60Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Non-smoking
  • English or French speaking
  • Ability to provide informed consent
  • Aged 60 to 85 years
  • 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 sitting
  • Physical activity restrictions due to diseases like intermittent claudication, renal impairment, active proliferative retinopathy, unstable cardiac or pulmonary disease, disabling stroke, or severe arthritis
  • Use of or medication changes 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)

Exposure

Duration - 10 hours per exposure session

Participants are exposed to a 10-hour simulated indoor overheating session under different temperature and humidity conditions.

Multiple exposure sessions on separate days depending on assigned conditions

Trial Site Locations

Total: 1 location

1

University of Ottawa

Ottawa, Ontario, Canada, K1N6N5

Actively Recruiting

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Research Team

G

Glen P Kenny, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

4

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