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Average ANKLE GO Score in the Objective Functional Assessment of the Ankle in Healthy Military Personnel (ANKMIL)

NCT07344493 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2026-01-15

No results posted yet for this study

Summary

This research aims to establish reference values for the Ankle-Go score, a validated tool for functional assessment of the ankle, in healthy military personnel. The Ankle-Go score, already used in the civilian population after sprains or surgery, combines physical tests and subjective questionnaires to assess functional recovery of the ankle. No normative data currently exist for the military population, whose physical and operational requirements differ significantly from those of the general population. This is an observational, prospective, single-center study conducted at the 39th medical branch in Oberhoffen (5th CMA). It will include 96 active military personnel with healthy ankles, examined during their periodic medical visit. Participants will complete the full Ankle-Go test and fill out the associated questionnaires on the secure anklego.com platform. The data will then be analyzed anonymously to calculate a reference average and explore possible variations according to gender and age. These results will ultimately improve care and fitness-to-duty decisions after ankle injuries in the military. The total duration of the study is estimated at 8 months, including 6 months of data collection and 2 months of analysis.

Conditions

  • Ankle Disorders Injuries

Sponsors & Collaborators

  • Direction Centrale du Service de Santé des Armées

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-07
Primary Completion
2025-11-08
Completion
2025-11-08

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07344493 on ClinicalTrials.gov