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Heat Stress and Physiological Strain of Permeable vs. Impermeable CB Protective Garment

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01221012
Enrollment
12
Registered
2010-10-14
Start date
2010-12-31
Completion date
2014-12-31
Last updated
2012-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heat Tolerance

Brief summary

Current protective clothing of any kind, especially the nuclear-biological-chemical (NBC) protective garments, amplify thermal stress because of the inherent properties of the clothing material. High insulation coefficient and low water vapor permeability of the protective cloth limit the ability of sweat to readily evaporate, which consequently result with a significant elevation of body temperature and with excessive body fluid loss (because of inefficient sweating) that might result with significant dehydration. Combat soldiers require to perform intense physical activities under hostile environmental conditions, including in contaminated areas that need the use of protective garments. The ability to fulfill a mission derives from the soldier's professionalism and from his physiological limits. It is well established that wearing protective garments affect tolerance time (TT) and performance. To operate in contaminated areas suitable protective garments should be worn. The inherent characteristics of the current protective garments limit, however, the effective working periods with such an ensemble, which is further aggravated in hot climate. Thus, in an attempt to increase TT and enhance work effectiveness, improved protective garments, which result with a lessened heat-stress, are under different stages of development. The relative influence of air permeability properties, garment weight and garment construction on heat stress and physiological strain will be investigated. The results will be quantified in terms of body temperatures, heart rate, fluid balance, subjective sensation and the maximum wear time (if necessary extrapolated).

Interventions

None listed

Sponsors

Medical Corps, Israel Defense Force
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL

Eligibility

Sex/Gender
MALE
Age
20 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Twelve young (20-30 yr) male subjects will voluntarily participate in this study. The potential participants will be informed of the study's nature, purpose and medical risks. Their inclusion in the study requires the medical clearance by the study's physician (CRF) and after having filled out and sign an informed consent form

Exclusion criteria

* heart conditions, blood pressure higher than 140/90 mmHg, known diabetes or any skin illness or lesions. Also be excluded are potential participants who were ill during the 2 weeks prior to the study

Design outcomes

Primary

MeasureTime frameDescription
The physiological burden of different CB Protective Garments1 yearThe physiological burden of different CB Protective Garments will be mesured by a heat tolerance test (HTT). The subjects will undergo an HTT wearing different CB Protective Garments and the results which indicate physiological burden will be compared between the different garments.

Secondary

MeasureTime frameDescription
Rectal temperature1 yearThe rectal temperature will be mesured by rectal thermistore.
Skin temperature1 yearThe skin temperature will be mesured by skin thermistores conected to 3 different sites (chest, leg and arm).
Heart rate1 yearHeart rate will be mesured by a polar watch.
Sweat rate1 yearThe sweat rate will be calculated in each HTT from the subject's weight before and after the test and his water balance.

Countries

Israel

Contacts

Primary ContactAmit Druyan, M.D
Amit.Druyan@sheba.health.gov.il972-03-7377180

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026