- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07344493
Average ANKLE GO Score in the Objective Functional Assessment of the Ankle in Healthy Military Personnel (ANKMIL) (ANKMIL)
January 6, 2026 updated by: Direction Centrale du Service de Santé des Armées
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.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
96
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
France
-
Haguenau, France, France, 67504
- Cma05/Am039
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Active military personnel in good health and performing operational duties (mainly infantrymen).
Participants are recruited during periodic medical examinations at the 39th medical centre in Oberhoffen.
Description
Inclusion Criteria:
- Active military personnel assigned to the 39th Medical Unit in Oberhoffen (5th CMA).
- Engaged in regular physical activity.
- Ankle considered healthy (no recent history of injury or instability).
- Verbal and written consent obtained.
Exclusion Criteria:
- History of ankle sprain, fracture, or surgery in the last 12 months.
- Musculoskeletal or neurological condition affecting walking or balance.
- Refusal to participate or withdrawal of consent.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Average Ankle-Go score in healthy military personnel
Time Frame: 6 months after the start of data collection
|
Establish the mean value, standard deviation and reference intervals for the Ankle-Go score in a population of healthy military personnel, based on data collected during the complete test (physical tests and questionnaires).
All these measurements correspond to a score (for example, for time in seconds, a patient performing exercise in 5 seconds, get a score of 2).
All scores will be added together to obtain a single value considered as the final score.
|
6 months after the start of data collection
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 7, 2025
Primary Completion (Actual)
November 8, 2025
Study Completion (Actual)
November 8, 2025
Study Registration Dates
First Submitted
November 19, 2025
First Submitted That Met QC Criteria
January 6, 2026
First Posted (Actual)
January 15, 2026
Study Record Updates
Last Update Posted (Actual)
January 15, 2026
Last Update Submitted That Met QC Criteria
January 6, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025PPRC07
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.