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Auxiliary Device to Alleviate Soldiers' Backload

Auxiliary Device to Alleviate Soldiers' Backload

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01565876
Acronym
minkal
Enrollment
12
Registered
2012-03-29
Start date
2012-12-31
Completion date
2014-01-31
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

Physiological Strain of Weight Bearing.

Keywords

weight bearing, physiological load

Brief summary

Combat soldiers are required to perform under strenuous physical conditions; hence, their physical fitness is a crucial factor in their survivability. The Auxiliary Device- Minkal, is suggested (by its manufactures) to be able to reduce the soldiers' physiological strain by lowering the absolute load being carried by the soldier. As a result, it may improve the soldier's physiological abilities and performance through enduring missions with heavy loads, and may lead to better protection on the soldier from overuse injuries.

Interventions

DEVICEMinkal- Auxiliary device to alleviate backload

The participants will undergo 6 days of study. The first day of the study include medical examination, maximal oxigen consumption day and anthropometric mesurments. Then The participants will undergo heat tolerance test 5 times (in different days). first day- without load. second day- with back load of 40% of the body weight. third day- with back load of 40% of the body weight and the Auxilairy Device. fourth day- with back load of 60% of the body weight. fifth day- with back load of 60% of the body weight and the Auxilairy Device. The rectal temperature, skin teperature and heart rate will be mesured each day and compered afterwards.

Sponsors

Medical Corps, Israel Defense Force
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
21 Years to 28 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy subjects without any of the following: chronic background diseases, cardiovascular, lung or respiratory, heat stroke history, headaches,psychiatric background, musculoskeletal problems, and without drugs use. * Lack of any acute disease during 2 weeks prior the study. * Subjects will give their written consent for participating the study after being informed by the study's physician about the study's aims, importance and the possible risks.

Exclusion criteria

* Rectal temperature above 39 Celsius degrees. * HR above maximal HR ( calculated as 220-age) * The subject's will to stop the test. * The researcher's/doctor's judgment.

Design outcomes

Primary

MeasureTime frameDescription
Physiological Load with and without the auxiliary device6 days for each patient.The physiological load will be measured using a heat tolerance test(HTT). Each paricipant will undergo a HTT 5 times (in different days). first day- without load. second day- with back load of 40% of the body weight. third day- with back load of 40% of the body weight and the Auxilairy Device. fourth day- with back load of 60% of the body weight. fifth day- with back load of 60% of the body weight and the Auxilairy Device. The rectal temperature, skin teperature and heart rate will be mesured in each HTT and compered afterwards to assess the physiological load.

Secondary

MeasureTime frameDescription
Rectal temperature6 daysThe Rectal temperature will be mesured by a rectal thermistore during each HTT.
Skin temperature6 daysThe Skin temperature will be mesured by skin thermistores on three sites (chest, leg and arm).
Heart Rate6 daysHeart rate will be monitored using a polar watch.
Sweat Rate6 daysSweat rate will be calculated from the patient's weight and his water balance.

Countries

Israel

Outcome results

None listed

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