NCT07261202

Brief Summary

Communities worldwide are experiencing increasing heat extremes that challenge the limits of human thermoregulation, particularly among vulnerable populations such as children. Compared with adults, children are more susceptible to heat related illness due to less efficient thermoregulatory systems and difficulty recognizing early signs of heat stress. In addition, prolonged heat exposure can adversely affect their mental health, contributing to cognitive decline, heightened anxiety, and irritability. As children spend substantial time in hot environments at school and at home, and as these conditions intensify with climate change, actions to safeguard their health are essential. Yet our understanding of heat exposure effects in children remains incomplete, hindering the development of evidence based strategies to protect them. To address this gap, the investigators aim to evaluate whether an indoor temperature limit of 26 °C (45 percent relative humidity), the upper threshold recommended to protect older adults, can effectively prevent dangerous increases in physiological strain and declines in cognitive function in children during a simulated daylong heatwave. The preliminary study will assess physiological and cognitive responses in children aged 10 to 15 years during a 6 hour exposure (approximating a typical school day) to two conditions: (1) the recommended indoor temperature upper limit (26 °C) and (2) a high heat condition representative of homes and schools without air conditioning during extreme heat events (36 °C). In both conditions, children will remain seated at rest while wearing light clothing (t shirt and shorts), with the exception of performing 15 minutes of stepping exercise (6-6.5 METS) each hour (excluding the lunch period) to reflect typical daily activity in a school setting. This experimental design will allow investigators to determine whether maintaining indoor temperatures at the recommended upper limit for older adults sufficiently mitigates physiological strain in children.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
8mo left

Started Nov 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress43%
Nov 2025Dec 2026

Study Start

First participant enrolled

November 8, 2025

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

November 21, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 3, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

7 months

First QC Date

November 21, 2025

Last Update Submit

April 20, 2026

Conditions

Keywords

Indoor overheatingIndoor temperaturesHeat waveThermoregulationAdolescentHeat strainHeat vulnerabilityHyperthermiaYouthThermal comfortPhysical activity

Outcome Measures

Primary Outcomes (1)

  • Core temperature (Peak) during daylong exposure to indoor overheating

    Peak visceral temperature (15 min average) during exposure. Visceral temperature is measured continuously throughout the 6 hour exposure to the simulated indoor overheating.

    End of 6 hour daylong exposure

Secondary Outcomes (28)

  • Profiles of Mood States (POMS) during daylong exposure to indoor overheating

    At the start (hour 0) and end of 6 hour daylong exposure

  • Environmental Symptoms Questionnaire (ESQ) during daylong exposure to indoor overheating

    At the start (hour 0) and end of 6 hour daylong exposure

  • Perceived exertion scale during daylong exposure to indoor temperature limit.

    At the start (hour 0) and end of 6 hour daylong exposure

  • Activity levels during daylong exposure to indoor overheating

    End of 6 hour daylong exposure

  • Feel good scale during daylong exposure to indoor overheating

    At the start (hour 0) and end of 6 hour daylong exposure

  • +23 more secondary outcomes

Study Arms (2)

Exposure to indoor temperature upper limit of 26°C

EXPERIMENTAL

Participants exposed daylong (6 hours) to an indoor temperature maintained at 26°C and 45% relative humidity (humidex equivalent of 29).

Other: Simulated exposure to indoor overheating

Exposure to hot indoor environment of 36°C

EXPERIMENTAL

Participants exposed daylong (6 hours) to an indoor temperature maintained at 36°C and 45% relative humidity (humidex equivalent of 45).

Other: Simulated exposure to indoor overheating

Interventions

Children exposed to a 6-hour simulated heat exposure

Exposure to hot indoor environment of 36°CExposure to indoor temperature upper limit of 26°C

Eligibility Criteria

Age10 Years - 15 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • English or French speaking.
  • Ability to provide informed assent.

You may not qualify if:

  • Chronic health conditions
  • Endurance exercise training (greater than 3 sessions of vigorous exercise training per week for 30 minutes or more)
  • Restrictions to physical activity

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Ottawa

Ottawa, Ontario, K1N 6N5, Canada

RECRUITING

MeSH Terms

Conditions

Heat Stress DisordersHyperthermiaMotor Activity

Condition Hierarchy (Ancestors)

Wounds and InjuriesBody Temperature ChangesSigns and SymptomsPathological Conditions, Signs and SymptomsBehavior

Study Officials

  • Glen P Kenny, PhD

    University of Ottawa

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Glen P Kenny, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Full Professor, University Research Chair

Study Record Dates

First Submitted

November 21, 2025

First Posted

December 3, 2025

Study Start

November 8, 2025

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

April 23, 2026

Record last verified: 2026-04

Locations