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Enrolling by invitationNCT07781592Updated Nov 10, 2026

Exercise Intensity and Heat Responses in Children and Youth

An interventional study of Low-Intensity Exercise in the Heat and Moderate-Intensity Exercise in the Heat in Body Temperature Changes, Heat Stress and Child Development, sponsored by University of Ottawa. Enrolling by invitation at 1 site in Canada. Open to female participants aged 9 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by University of Ottawa · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
9 Years to 25 Years
Sex
Female
01

Study summary

Little is known about how children and youth regulate body temperature during exercise in the heat compared with young adults, including whether differences in whole-body heat exchange contribute to their responses. The goal of this clinical trial is to determine how exercise intensity affects thermoregulation in boys and girls aged 9-16 years compared with young adult men and women aged 20-25 years. Participants will complete three study visits in a hot environment of 36°C (degree Celcius (97°F, degree Farenheit)), performing light-, moderate-, and vigorous-intensity exercise corresponding to metabolic heat production of 120, 160, and 200 W/m² (w=watts, m=meter), respectively. During each visit, participants will complete four 15-minute bouts of exercise (i.e., bout 1, 2, 3 and 4 respectively) separated by 15-minute rest periods. Testing will be performed in a whole-body air calorimeter, a specialized chamber that precisely measures heat lost through evaporation and dry heat exchange and the amount of heat stored in the body. These measurements, together with core temperature and heart rate, will allow researchers to determine how increasing exercise intensity affects the body's ability to lose heat and whether these responses differ between children and youth and young adults.

02

Conditions studied

  • Body Temperature Changes
  • Heat Stress
  • Child Development
  • Heat
  • Physiological Stress

Keywords

  • Thermoregulation
  • Heat loss
  • Heat strain
  • Heat tolerance
  • Exercise-heat stress
03

In context

Body Temperature Changes

97 studies on the registry are indexed under Body Temperature Changes; 20 are open to participants now.

This study's planned enrollment of 12 is below the median of 40 across 68 interventional studies indexed under Body Temperature Changes.

Browse Body Temperature Changes studies →

Lead sponsor

University of Ottawa is the lead sponsor of 125 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
9 Years to 25 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthy male or female.
  • Aged 9-16 years or 20-25 years.
  • Habitually active, defined as participating in regular physical activity at least 3 times per week for at least 20 minutes per session over the previous 6 months.
  • Able to understand and communicate in English or French.
  • For participants younger than 18 years, written parental or guardian consent and participant assent are required.

Exclusion criteria

Exclusion Criteria:

  • Acute illness at the time of testing (e.g., cold, flu, or infection).
  • History of a chronic medical condition that may affect thermoregulation, cardiovascular function, or exercise capacity (e.g., cardiovascular disease, metabolic disorders, respiratory disease including asthma requiring regular medication, or neurological disorders).
  • Use of medications known to affect thermoregulation, hydration status, or cardiovascular responses.
  • History of heat-related illness (e.g., heat exhaustion or heat stroke).
  • Digestive abnormalities or gastrointestinal conditions that may contraindicate ingestion of a telemetry pill.
  • Any condition that, in the opinion of the investigators, would compromise participant safety or the integrity of the data.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
12 participants (estimated)

Study arms

  • Experimental
    Low-intensity exercise

    Participants will complete intermittent light-intensity exercise in a hot environment of 36°C (degree Celsius (97°F, degree Fahrenheit)). Exercise will be performed at a metabolic heat production of 120 W/m² (W=watts; m=meter) and will consist of four 15-minute exercise periods separated by 15-minute rest periods. Exercise workload will be individually adjusted to achieve the prescribed metabolic heat production.

    Other: Low-Intensity Exercise in the Heat

  • Experimental
    Moderate-intensity exercise

    Participants will complete intermittent moderate-intensity exercise in a hot environment of 36°C (97°F). Exercise will be performed at a metabolic heat production of 160 W/m² and will consist of four 15-minute exercise periods separated by 15-minute rest periods. Exercise workload will be individually adjusted to achieve the prescribed metabolic heat production.

    Other: Moderate-Intensity Exercise in the Heat

  • Experimental
    Vigorous-intensity exercise

    Participants will complete intermittent vigorous-intensity exercise in a hot environment of 36°C (97°F). Exercise will be performed at a metabolic heat production of 200 W/m² and will consist of four 15-minute exercise periods separated by 15-minute rest periods. Exercise workload will be individually adjusted to achieve the prescribed metabolic heat production.

    Other: Vigorous-Intensity Exercise in the Heat

Interventions

  • OtherLow-Intensity Exercise in the Heat

    Participants complete intermittent low-intensity exercise at a metabolic heat production of 120 W/m² (w=watts; m=meter) in a hot environment of 36°C (degree Celsius (97°F, degree Fahrenheit)).

  • OtherModerate-Intensity Exercise in the Heat

    Participants complete intermittent moderate-intensity exercise at a metabolic heat production of 160 W/m² in a hot environment of 36°C (97°F).

  • OtherVigorous-Intensity Exercise in the Heat

    Participants complete intermittent vigorous-intensity exercise at a metabolic heat production of 200 W/m² in a hot environment of 36°C (97°F).

06

What researchers measure

Primary outcomes

  1. Core temperature

    Core temperature indexed by visceral (telemetry pill) temperature

    Time frame: End of each of the four 15 minutes exercise bouts (average of last 5 minutes)

Secondary outcomes

  1. Evaporative heat loss

    Evaporative heat loss as assessed using a direct air calorimeter.

    Time frame: End of each of the four 15 minutes exercise bouts (average of last 5 minutes)

  2. Dry heat loss

    Dry heat loss as assessed using a direct air calorimeter.

    Time frame: End of each of the four 15 minutes exercise bouts (average of last 5 minutes)

  3. Whole-body total heat loss

    Total heat loss (dry + evaporative) as assessed using a direct air calorimeter

    Time frame: End of each of the four 15 minutes exercise bouts (average of last 5 minutes)

  4. Body Heat Storage

    Heat stored in the body for each of the exercise bouts

    Time frame: Change from start to the end for each of the four 15 minutes exercise bouts

  5. Skin Temperature

    Skin temperature measured at 8-sites (forehead, chest, scapula, upper arm, forearm, hand, thigh, calf) with mean value calculated as weighted value of 8 sites - forehead, 7%; chest, 17.5%; scapula, 17.5%, upper arm, 7%; forearm, 7%; hand, 5%; thigh, 19%; and calf, 20%.

    Time frame: End of each of the four 15 minutes exercise bouts (average of last 5 minutes)

  6. Change in skin temperature

    Skin temperature measured at 8-sites (forehead, chest, scapula, upper arm, forearm, hand, thigh, calf) with mean value calculated as weighted value of 8 sites - forehead, 7%; chest, 17.5%; scapula, 17.5%, upper arm, 7%; forearm, 7%; hand, 5%; thigh, 19%; and calf, 20%.

    Time frame: Change from start to the end for each of the four 15 minutes exercise bouts

  7. Heart rate

    Measured continuously with chest-band device

    Time frame: End of each of the four 15 minutes exercise bouts (average of last 5 minutes)

  8. Thermal Sensation Scale

    Thermal sensation will be assessed using the American Society of Heating, Refrigerating and Air-Conditioning Engineers (ASHRAE) 7-point scale ("0=neutral to 7=extremely hot")

    Time frame: End of each of the four 15 minutes exercise bouts (average of last 5 minutes)

07

Study locations

1 site
08

Updates

1 registry update since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date
1 update, last Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    Minor edits only
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07781592
Responsible party
Glen P. Kenny (Full Professor, University of Ottawa) — Principal investigator
First posted
Aug 24, 2026
Start date
Jul 21, 2026
Primary completion
Apr 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Nov 10, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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