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NCT Number: NCT07261202

Impact of Indoor Overheating on Physiological Strain in Children

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.

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Key information

Age range

10 year–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Ottawa

Ottawa, Ontario, K1N 6N5, Canada

Location status: Recruiting

Location contact

Glen P Kenny, PhD

CONTACT

[email protected]

613-562-5800 ext. 4282

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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

Treatment and study plan

Simulated exposure to indoor overheating

Other

Children exposed to a 6-hour simulated heat exposure

Primary outcomes

  1. Core temperature (Peak) during daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

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

Secondary outcomes

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

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

    Potential changes in mood (7 subscales of mood: tension, anger, depression, fatigue, confusion, vigor and esteem related affect). The POMS-40 is a validated, self-administered questionnaire that examines seven distinct aspects of mood state across two positive subscales (Esteem-Related Affect, and Vigor) and five negative subscales (Fatigue, Tension, Confusion, Anger, and Depression), which are described across 40 distinct adjectives. For each individual item, participants were asked to describe "how you feel right now" by responding using a 5-point Likert scale (0 = "Not at all", 1 = "A little", 2 = "Moderately", 3 = "Quite a lot", or 4 = "Extremely"). The values of items associated with a specific subscale (e.g., Fatigue) were summed to calculate its score.

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

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

    Self-reported environmental reactions and medical symptomatology associated with prolonged heat exposure. The ESQ-IV is a validated 68-item, self-administered questionnaire that has been used successfully in identifying symptomatology during exposure to a wide variety of environmental conditions, including heat exposure.

    Participants are asked to assess and described "how you have been feeling today" by responding to each item using a 6-point Likert scale (0 = "Not at all", 1 = "Slight", 2 = "Somewhat", 3 = "Moderate", 4 = "Quite a bit", or 5 = "Extreme"). Total Symptom Score was calculated from this data by taking the sum of the intensity ratings from all 68 individual items using reverse scores for the three positive items from the list ("I Felt Good", "I Felt Alert", and "I Felt Wide Awake").

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

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

    Perceived exertional assessed via a visual analog scale ("How hard are you working?") ranging from "no exertional at all" to "maximal exertion"

  4. Activity levels during daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Activity levels assessed via a wearable monitor (Actical) containing an accelerometer worn on the wrist and hip.

  5. Feel good scale during daylong exposure to indoor overheating

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

    Feel good scale assessed via a visual analog scale (How good do you feel?) ranging from "very good" to "very bad" (midpoint: neutral)

  6. Thirst sensation scale during daylong exposure to indoor overheating

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

    Thirst sensation assessed via a visual analog scale ranging from very, very thirsty to not thirsty at all.

  7. Thermal comfort scale during daylong exposure to indoor overheating

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

    Thermal comfort assessed via a visual analog scale ("How comfortable does your body temperature feel?") ranging from "very uncomfortable" to "comfortable".

  8. Thermal sensation 2 scale during daylong exposure to indoor overheating

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

    Thermal sensation assessed via a visual analog scale ("How do you feel?") ranging from "hot" to "cold"(midpoint: neutral)

  9. Thermal sensation scale during daylong exposure to indoor overheating

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

    Thermal sensation assessed via a visual analog scale (How hot do you feel?) ranging from "extremely hot" to "neutral".

  10. Fluid loss during daylong exposure to indoor overheating

    Time frame: At end of 6 hour daylong exposure

    Fluid loss calculated as the change in body mass during each exposure presented as a percentage of baseline body mass (corrected for food consumption).

  11. Fluid consumption during daylong exposure to indoor overheating

    Time frame: At end of 6 hour daylong exposure

    Average hourly fluid consumption calculated by weighing participant water intake at the start and end of each hour of exposure (normalized to the exposure duration).

  12. Hydration status during daylong exposure to indoor overheating

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

    Hydration status measured via assessing the urine specific gravity of a urine sample.

  13. BTrackS Balance Assessment during daylong exposure to indoor overheating (postural stability).

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

    To assess postural stability, participants will be asked to stand on a BTracks force plate with their feet spread out to shoulder width, hand on their hips and eyes closed. The assessment will comprise of four trials (one practice trial) lasting 20 seconds in length and 20 seconds between trials. Center of pressure (COP) vector data along vertical (y) and horizontal (x) axes will be summed for the total path excursion length (cm) during each trial

  14. Executive function during daylong exposure to indoor overheating (cognitive function).

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

    Participants will be provided with a tablet device with the Sway Medical testing platform for the assessment of executive function. Participants will complete the Cued Stroop test, in which they are presented a sequence of congruent, neutral and incongruent color-word tasks.

  15. CDC 4-Stage Balance Test during daylong exposure to indoor overheating (postural stability).

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

    To assess postural stability, participants hold a tablet to their chest, then auditory cues guide participants through four consecutive stances, feet side by side, instep of one foot touching the big toe of the other foot, tandem stand with one foot in front of the other, heel touching toe, and stand on one foot. The balance assessment will be evaluated based on movement detected by an accelerometer integrated into the hardware of the tablet device (Sway Medical Inc).

  16. Memory recall during daylong exposure to indoor overheating (cognitive function).

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

    Participants will be provided with a tablet device with the Sway Medical testing platform for the assessment of memory recall. Participants complete both a delayed recall test and a working memory test.

  17. Impulse control during daylong exposure to indoor overheating (cognitive function).

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

    Participants will be provided with a tablet device with the Sway Medical testing platform for the assessment of impulse control. Participants will be asked to respond to both "go" and "no-go" visual cues. In response to the "go" cue, participants will initiate a movement of the device.

  18. Reaction time during daylong exposure to indoor overheating (cognitive function).

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

    Participants will be provided with a tablet device with the Sway Medical testing platform for the assessment of reaction time. Participants will be asked to initiate a movement of the device in response to a visual cue.

  19. Diastolic blood pressure during daylong exposure to indoor overheating.

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

    Diastolic blood pressure measured in triplicate via automated oscillometry (~60 seconds between measures).

  20. Systolic blood pressure during daylong exposure to indoor overheating

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

    Systolic blood pressure measured in triplicate via automated oscillometry (~60 seconds between measures).

  21. Heart rate end of daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Heart rate measured at hour 6 of exposure to indoor overheating (15-min average).

  22. Heart rate (AUC) during daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Areas under the curve (AUC) of heart rate during the 6 hour exposure to the simulate indoor overheating.

  23. Heat rate (Peak) during daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Peak heart rate (15 min average) during exposure. Heart rate is measured continuously throughout the 6 hour exposure to the simulated indoor overheating.

  24. Mean skin temperature end of daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Mean skin temperature measured over 7 body regions at hour 6 of exposure to indoor overheating (15-min average).

  25. Mean skin temperature (AUC) during daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Areas under the curve (AUC) of mean skin temperature as calculated over 7 body regions during the 6 hour exposure to the simulate indoor overheating.

  26. Mean skin temperature (Peak) during daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Peak mean skin temperature (15 min average) during exposure. Mean skin temperature as calculated from skin temperature measured across 7 body regions is measured continuously throughout the 6 hour exposure to the simulated indoor overheating.

  27. Core temperature end of daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Visceral temperature measured at hour 6 of exposure to indoor overheating (15-min average).

  28. Core temperature (AUC) during daylong exposure to indoor overheating

    Time frame: End of 6 hour daylong exposure

    Areas under the curve (AUC) of visceral temperature during the 6 hour exposure to the simulate indoor overheating.

Study contacts

Contact information is provided by the study sponsor or research team.

Glen P Kenny, PhD

CONTACT

[email protected]

613-562-5800 ext. 4282

Sponsors and collaborators

Lead sponsor

University of Ottawa

Other

Registry information

Official study title

A Preliminary Study Assessing the Effectiveness of a 26 °C Indoor Temperature Limit on Physiological Responses in Children

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 3, 2025
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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