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Clinical Trials/NCT01596543
NCT01596543
Completed
Not Applicable

Thr Effect of Partial and Complete Sleep Deprivation on Heat Tolerance

Sheba Medical Center1 site in 1 country12 target enrollmentNovember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep Deprivation
Sponsor
Sheba Medical Center
Enrollment
12
Locations
1
Primary Endpoint
oxygen consumption
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of the present study is to evaluate the effect of partial and complete sleep deprivation on exercise heat tolerance. Twelve healthy young male volunteers will participate in the study. They will arrive to our lab four times, in each visit the will undergo VO2 test and Heat Tolerance Test (HTT) after sleeping different amount of hours.

Detailed Description

The volunteers will arrive to our lab fout times- During their first visit they will go through a VO2 max test in order to evaluate their aerobic fitness, and their physiological efficiency will be measured. During their second visit they will go through an exercise heat tolerance test according to our validated protocol after a full night sleep. During the third and fourth visit they will go through an exercise heat tolerance test and a measurement of their physiological efficiency after a partial and complete sleep deprivation, respectively. The physiological tests will take place in the heat chamber that is located at the Heller Institute of Medical Research. The results will be then analyzed, and a comparison between the physiological measurements during the heat tolerance tests and the physiological efficiency tests after the various sleep conditions will be performed.

Registry
clinicaltrials.gov
Start Date
November 2012
End Date
May 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age 18-30
  • after medical checkup
  • after signing concent form

Exclusion Criteria

  • heart disease
  • respiratory disease
  • baseline bp above 140/90 mmHg
  • sleep disorders
  • anhydrosis
  • skin disease
  • acute illness

Outcomes

Primary Outcomes

oxygen consumption

Time Frame: experimental days 1,3,4

volunteer's oxygen consumption (VO2) will be monitored continuously with a metabolic chart (ZAN), while running for 10 min on a treadmill under comfortable environmental conditions.Each volunteer will undergo the test 4 times.

Secondary Outcomes

  • Skin temperature(experimental days 2,3,4)
  • Rectal temperature(experimental days 2,3,4)
  • Heart rate(experimental days 1,2,3,4)

Study Sites (1)

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