Actively Recruiting
A Preliminary Study Assessing the Effectiveness of a 26 6C Indoor Temperature Limit on Physiological Responses in Children
Led by University of Ottawa · Updated on 2026-04-23
10
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Children are more vulnerable to heat-related illnesses than adults due to less efficient body temperature control and difficulty noticing early heat stress signs. This trial evaluates whether keeping indoor temperatures at 26 6C with 45% humidity, a limit recommended for older adults, can reduce physical strain and cognitive decline in children aged 10 to 15 during simulated daylong heatwaves. The study aims to fill gaps in understanding how heat affects children's health, especially as climate change increases heat exposure. Participants experience two conditions in a randomized, single-blind setup: one with indoor temperature maintained at 26 6C and another at 36 6C, both with 45% humidity. Each exposure lasts six hours, mimicking a typical school day. During this time, children wear light clothing and perform 15 minutes of stepping exercise each hour except lunch, simulating normal school activity levels. During the study, children remain seated mostly at rest while researchers monitor various measures including peak core temperature, heart rate, blood pressure, hydration status, mood states, cognitive functions like memory and impulse control, and balance. Assessments occur at the start and end of the exposure, with fluid consumption and loss recorded. This detailed monitoring aims to understand how indoor temperature limits impact children's physiological and cognitive responses during heat exposure.
CONDITIONS
Brief Title
Impact of Indoor Overheating on Physiological Strain in Children
Who Can Participate
Eligibility Criteria
You may qualify if you...
- English or French speaking
- Ability to provide informed assent
- Aged between 10 and 15 years
You will not qualify if you...
- Chronic health conditions
- Endurance exercise training exceeding 3 sessions per week of vigorous exercise lasting 30 minutes or more
- Restrictions to physical activity
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 - Each exposure lasts 6 hours; exposures occur in a crossover design with a washout period in between
Participants undergo two separate daylong (6-hour) exposures to controlled indoor temperatures of 26°C and 36°C to assess physiological responses.
2 daylong visits (in-person), one for each temperature exposure
Trial Site Locations
Total: 1 location
1
University of Ottawa
Ottawa, Ontario, Canada, K1N 6N5
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
2
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