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Assessing Foot Injuries in Infantry Recruits Wearing Different Boots

Assessing Foot Injuries in Infantry Recruits Wearing Different Boots, a Prospective Randomized Study

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02810002
Enrollment
98
Registered
2016-06-22
Start date
2014-08-31
Completion date
2015-02-28
Last updated
2016-06-22

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

Conditions

Abrasion, Ankle Sprain, Back Pain, Blister, Patellofemoral Pain Syndrome, Stress Fracture

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.

Interventions

DEVICEExperimental infantry boot - DEFINITE-REGULATOR

Training: infantry basic training in the experimental boots

DEVICEControl infantry boot

Training: infantry basic training in the control boots

Sponsors

Medical Corps, Israel Defense Force
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Infantry recruits on selected base

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Number of recruits with at least one injury related to the boots14 weeksInjuries assessed: Blister, Abrasion, Stress Fracture, Ankle Sprain, Patellofemoral Pain Syndrome, Back Pain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026