Actively Recruiting
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
Eligibility Criteria
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
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
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 - 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
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