Assessing Foot Injuries in Infantry Recruits Wearing Different Boots

Status Completed

Clinical Trial Summary

One hundred infantry recruits will be randomly assigned to two groups. Injuries will be monitored.

Clinical Trial Description

One hundred infantry recruits will be randomly assigned to receive experimental infantry boots (DEFINITE-REGULATOR) or standard issued boots (modified Belleville 390 TROP).

Overuse injuries and foot injuries will be monitored over a period of 14 weeks. The intervention group will wear experimental infantry boots and the controls will wear standard issue boots. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02810002
Study type	Interventional
Source	Medical Corps, Israel Defense Force
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	August 2014
Completion date	February 2015

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