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The Effect of Ventilated Vest on Thermoregulation During Exercise in Hot Environment

S

Sheba Medical Center

Status

Unknown

Conditions

Body Temperature Changes

Treatments

Other: Research intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT01863927
1178-12 (Other Identifier)
SHEBA-12-9726-AD-CTIL

Details and patient eligibility

About

The purpose of this preliminary experiment is to measure the effect of a novel ventilation system on the physiological strain during exercise in high heat load while wearing ballistic protective vest. Ten young and healthy participants will participate in the study. They will all go through a six days heat acclimation period in a heat chamber according to a valid protocol. Afterwards they will be randomly exposed to 4 conditions during four separate consecutive days.

Full description

Ten young and healthy civilian participants will participate in the study. They will all go through a six days heat acclimation period in a heat chamber according to a valid protocol. After heat acclimation the participant will be randomly exposed to 4 conditions during four separate consecutive days: 1) walking on a treadmill for two hours in hot-wet conditions (30OC, 70% RH) while wearing military uniforms and a vest (control group); 2) walking on a treadmill for two hours in hot-dry conditions (40OC, 30% RH) while wearing military uniforms and a vest (control group); 3) walking on a treadmill for two hours in hot-wet conditions (30OC, 70% RH) while wearing military uniforms and a vest with a ventilator (experimental group); 4) walking on a treadmill for two hours in hot-dry conditions (40OC, 30% RH) while wearing military uniforms and a vest with a ventilator (experimental group). During the heat exposures, rectal temperature, skin temperature and heart rate will be continuously monitored. Subjective comfort measures, heat strain indices, sweat rate and sweat evaporation will be also measured/calculated. The differences in the above measures, during exposure to exercise in the heat between ventilator and no ventilator will be then analyzed.

Enrollment

10 estimated patients

Sex

Male

Ages

21 to 28 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age 21-28
  • healthy
  • after medical checkup
  • after signing concent form

Exclusion criteria

  • heart disease
  • respiratory disease
  • baseline bp above 140/90 mmHg
  • sleep disorders
  • diabetes
  • anhydrosis
  • skin disease
  • acute illness in last 3 days prior to the examination

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Research arm
Experimental group
Description:
Each of the participants will be randomly exposed to 4 conditions during four separate consecutive days.
Treatment:
Other: Research intervention

Trial contacts and locations

1

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Central trial contact

Barliz Adato, MD

Data sourced from clinicaltrials.gov

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