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Acute Sleep Deprivation on Whole-body Heat Exchange During Exercise-heat Stress in Young and Older Men

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University of Ottawa

Status

Completed

Conditions

Aging
Thermoregulation
Heat Exchange
Sleep Disturbance
Exercise

Treatments

Other: Sleep deprivation
Other: Normal sleep

Study type

Interventional

Funder types

Other

Identifiers

NCT05838014
HEPRU-2023-01

Details and patient eligibility

About

Sleep deprivation has long been thought to modulate thermoregulatory function. Seminal work on sleep deprivation and thermoregulation has demonstrated that sleep-deprived individuals experience greater elevations in core temperature during exercise-heat stress due to reductions in the activation of local heat loss responses of cutaneous vasodilation and sweating. However, it remains unclear 1) if reductions in local heat loss responses would compromise whole-body heat loss (evaporative + dry heat exchange) and 2) if differences exist, are they dependent on the heat load generated by exercise (increases in metabolic rate augments the rate that heat must be dissipated by the body). Further, much of the understanding of the effects of sleep deprivation on thermoregulation has been limited to assessments in young adults. Studies show that aging is associated with reduction in cutaneous vasodilation and sweating that compromise whole-body heat loss exacerbating body heat storage during moderate- and especially more vigorous-intensity exercise in the heat. However, it remains unclear if sleep deprivation may worsen this response in older adults.

The purpose of this study is therefore to evaluate the effects of sleep-deprivation on whole-body total heat loss during light, moderate, and vigorous exercise-heat stress and to assess if aging may mediate this response. To achieve this objective, direct calorimetry will be employed to measure whole-body total heat loss in young (18-30 years) and older (50-65 years) men during exercise at increasing, fixed rates of metabolic heat production of 150 (light), 200 (moderate), and 250 W/m2 (vigorous) in dry heat (40°C, ~15% relative humidity) with and without 24 hours of sleep deprivation.

Enrollment

21 patients

Sex

Male

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy young (18-30 years) and older males (50-65 years)
  • non-smoking
  • English or French speaking
  • ability to provide informed consent

Exclusion criteria

  • presence of chronic diseases (e.g., hypertension, diabetes)
  • acute illness (e.g., flu, COVID-19)
  • physical restriction limiting physical activity (e.g., severe arthritis, etc.)
  • use of medication judged by the patient or investigators to make participation in this study inadvisable
  • engaged in regular endurance training

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

21 participants in 2 patient groups

Normal sleep
Active Comparator group
Description:
Participants will complete three 30-minute bouts of semi-recumbent cycling at incrementally increasing fixed metabolic heat loads (150, 200 and 250 W/m2) in a hot, dry condition (40°C, 15% relative humidity). Each exercise bout will be separated by a 15 minute period of rest, with the final recovery 1 hour in duration. Exercise will commence between the hours of 7 AM and 9 AM following a period of normal sleep (\~8 hours) (Control condition).
Treatment:
Other: Normal sleep
Sleep deprivation
Experimental group
Description:
Participants will complete three 30-minute bouts of semi-recumbent cycling at incrementally increasing fixed metabolic heat loads (150, 200 and 250 W/m2) in a hot, dry condition (40°C, 15% relative humidity). Each exercise bout will be separated by a 15 minute period of rest, with the final recovery 1 hour in duration. Exercise will commence between the hours of 7 AM and 9 AM following a period of 24 hour of sleep deprivation (Sleep deprivation condition).
Treatment:
Other: Sleep deprivation

Trial contacts and locations

1

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Central trial contact

Fergus K O'Connor, PhD; Glen P Kenny, PhD

Data sourced from clinicaltrials.gov

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