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Assessing Foot Injuries in Infantry Recruits Wearing Different Boots

Phase 1
Completed
Conditions
Stress Fracture
Back Pain
Ankle Sprain
Abrasion
Patellofemoral Pain Syndrome
Blister
Registration Number
NCT02810002
Lead Sponsor
Medical Corps, Israel Defense Force
Brief Summary

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

Detailed 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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
98
Inclusion Criteria
  • Infantry recruits on selected base
Exclusion Criteria
  • None

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Number of recruits with at least one injury related to the boots14 weeks

Injuries assessed: Blister, Abrasion, Stress Fracture, Ankle Sprain, Patellofemoral Pain Syndrome, Back Pain

Secondary Outcome Measures
NameTimeMethod

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