Recruiting

Humidity & Heat

Sponsor:

University of Ottawa

Code:

NCT06842953

Conditions

Heat Stress

Physiological Stress

Eligibility Criteria

Sex: All

Age: 60 - 70+

Healthy Volunteers: Accepted

Interventions

Simulated indoor overheating

Study Details

Brief summary:

Laboratory-based studies show that exposure to high humidity can worsen the effects of heat stress in young and older adults by impeding sweat evaporation - the main mechanism by which the human body cools itself. At high levels of humidity, the efficiency of sweating decreases causing a greater rise core temperature and burden on the cardiovascular system. In this context, increasing temperatures and humidity with climate change thus pose a potential compound risk for human health. While humidity's role in heat-health outcomes could substantially alter projections of health burdens from climate change, the impact of humidity on physiological strain in vulnerable people in relation to the indoor environment has yet to be evaluated. In a recent study delineating the physiological effects of the proposed 26°C indoor upper limit (PMID: 38329752), relative humidity was set to 45% in all conditions based on indoor humidity standards by the American Society of Heating and Air-Conditioning Engineers. However, it is unknown whether a refinement of the recommended indoor temperature limit of 26°C is required in situations where humidity cannot be maintained at this level.

On separate occasions, the investigators will assess the change in body temperature and cardiovascular strain in older adults (65-85 years) exposed for 10 hours at the recommended indoor temperature limit of 26°C and 45% relative humidity (equivalent humidex of 29 (considered comfortable)) (experimental condition A), to 26°C with a relative humidity of 15% (equivalent humidex of 23 (considered comfortable); humidex is used to measure the perceived temperature taking into account the humidity)) (experimental condition B), to 26°C with a relative humidity of 85% (equivalent humidex of 37 (considered somewhat uncomfortable)) (experimental condition C), and to 31°C and 45% relative humidity with an equivalent humidex of 37 (considered somewhat uncomfortable) that is similar to experimental condition C. With this experimental design, investigators will assess the effects of indoor humidity in driving human heat strain and identify whether refinements in the recommended 26°C indoor temperature limit may be required. Further, by evaluating changes in relation to ambient conditions with a similar humidex, the investigators can assess how individuals perceive and respond to both heat and humidity.

Conditions

Heat Stress

Physiological Stress

Study ID

NCT06842953

Start date

Mar 14, 2025

Status verified date

Jun, 2025

Completion date

Sep 1, 2026

Anticipated

Primary completion date

Mar 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 60 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Non-smoking.
  • English or French speaking.
  • Ability to provide informed consent.
  • with or without a) chronic hypertension (elevated resting blood pressure; as defined by Heart and Stroke Canada and Hypertension Canada), b) type 2 diabetes as defined by Diabetes Canada, with at least 5 years having elapsed since time of diagnosis

Exclusion Criteria:

  • Episode(s) of severe hypoglycemia (requiring the assistance of another person) within the previous year, or inability to sense hypoglycemia (hypoglycemia unawareness).
  • Serious complications related to diabetes (gastroparesis, renal disease, uncontrolled hypertension, severe autonomic neuropathy).
  • Uncontrolled hypertension - BP >150 mmHg systolic or >95 mmHg diastolic in a sitting position.
  • Restrictions in physical activity due to disease (e.g. intermittent claudication, renal impairment, active proliferative retinopathy, unstable cardiac or pulmonary disease, disabling stroke, severe arthritis, etc.).
  • Use of or changes in medication judged by the patient or investigators to make participation in this study inadvisable.
  • Cardiac abnormalities identified during screening

Study Design

Enrollment

10 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

experimental: Exposure to recommended indoor temperature limit with normal indoor humidity

Participants exposed daylong (10 hours) to an indoor temperature maintained at 26°C and 45% relative humidity (humidex equivalent of 29).

experimental: Exposure to recommended indoor temperature limit with low indoor humidity

Participants exposed daylong (10 hours) to an indoor temperature maintained at 26°C and 15% relative humidity (humidex equivalent of 23).

experimental: Exposure to recommended indoor temperature limit with high indoor humidity

Participants exposed daylong (10 hours) to an indoor temperature maintained at 26°C and 85% relative humidity (humidex equivalent of 37).

experimental: Exposure to high indoor temperature with normal indoor humidity

Participants exposed daylong (10 hours) to an indoor temperature maintained at 31°C and 45% relative humidity (humidex equivalent of 37).

Interventions

Simulated indoor overheating

Older adults are exposed to a 10-hour simulated exposure

Primary outcome measure

  • Core temperature (Peak) during daylong exposure to indoor overheating [ Time Frame: End of 10 hour daylong exposure ]
  • Core temperature (AUC) during daylong exposure to indoor overheating [ Time Frame: End of 10 hour daylong exposure ]
  • Heat rate (Peak) during daylong exposure to indoor overheating [ Time Frame: End of 10 hour daylong exposure ]
  • Heart rate (AUC) during daylong exposure to indoor overheating [ Time Frame: End of 10 hour daylong exposure ]
  • Cardiac response to standing from supine (30:15 Ratio) during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Systolic Response to Standing From Supine during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Heart rate variability: RMSSD during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Heart rate variability: SDNN during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Thermal comfort scale during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Thirst sensation scale during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Arousal scale during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Fluid loss during daylong exposure to indoor overheating [ Time Frame: At end of 10 hour daylong exposure ]
  • Changes in plasma volume during daylong exposure to indoor overheating [ Time Frame: At end of 10 hour daylong exposur ]
  • Systolic blood pressure during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]
  • Rate pressure product during daylong exposure to indoor overheating [ Time Frame: At the start (hour 0) and end of 10 hour daylong exposure ]

Central Contacts and Locations

Central contacts

Locations

University of Ottawa

Recruiting

Ottawa, Ontario, Canada, K1N6N5

Contacts

More Information

Sponsor

University of Ottawa

Last update posted

Jun 15, 2025

Last verified

Jun, 2025

Keywords

  • Heat wave
  • Indoor overheating
  • Thermoregulation
  • Heat strain
  • Elderly
  • Heat vulnerability
  • Hyperthermia
  • Thermal comfort

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Ottawa on 2025-06-15.