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Clinical Trials/NCT04317027
NCT04317027UnknownNot Applicable

Physiological Examination of New Fighting Clothing During Exposure to Exercise Under Hot Conditions

Sheba Medical Center1 site in 1 country20 target enrollmentStarted: June 1, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
20
Locations
1
Primary Endpoint
Body temperature

Study Overview

Brief Summary

The use of fighting clothing under extreme heat conditions during rest and exercise, compromises the body's ability to maintain temperature within the narrow physiological range needed for regular function, and might lead to heat injury. Beside working and fighting clothing, the fighters also wear vests used for protection and equipment carrying, which leads to substantial reduction in effective dissipation area from the central region of the body. This fact is most substantial during exercise which increases metabolic heat production rate and leads to heat accumulation and rise in body temperature. Therefore the development of new textile technologies to allow rapid cooling during intervals is of great importance.

This study is designed to physiologically examine new textile solutions, by evaluating the physiological stress induced during exercise under mild heat conditions.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
20 Years to 28 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Formerly fighters
  • •Without prior diseases including heart, vessel, respiratory and metabolic diseases or known use of medications
  • •experience in using fighting clothing
  • •VO2max > 50 ml/kg/min

Exclusion Criteria

  • •Incapacity to fulfill inclusion criteria

Arms & Interventions

All subjects

Experimental

All subjects in this trial will receive the new fighting clothing while performing the study protocol

Intervention: New Fighting Clothing (Device)

Outcomes

Primary Outcomes

Body temperature

Time Frame: During intervention period (2 hours test) only

Using rectal thermometer

Heart rate

Time Frame: During intervention period (2 hours test) only

Using heart rate watch

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Dr. Sagi Arie Shpizer

Principal Investigator, Heller Institute of Medical Research

Sheba Medical Center

Study Sites (1)

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