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Completed

NCT Number: NCT02810002

Assessing Foot Injuries in Infantry Recruits Wearing Different Boots

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

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Infantry recruits on selected base

Exclusion criteria

  • None

Treatment and study plan

Experimental infantry boot - DEFINITE-REGULATOR

Device

Training: infantry basic training in the experimental boots

Control infantry boot

Device

Training: infantry basic training in the control boots

Primary outcomes

  1. Number of recruits with at least one injury related to the boots

    Time frame: 14 weeks

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

Sponsors and collaborators

Lead sponsor

Medical Corps, Israel Defense Force

Other

Registry information

Official study title

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

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jun 22, 2016
Registry last updated
Jun 22, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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