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Scientists uncover hidden foot muscle changes after ankle sprains

NCT ID NCT05815576

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study looked at how foot and ankle joints move and bear weight during running in people with chronic ankle instability, those who recovered from a sprain, and healthy individuals. Researchers used cameras and pressure plates to measure joint angles and forces, and ultrasound to check foot muscle size. The goal was to understand why some people develop long-term instability after an ankle sprain.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Intrinsic foot muscle fatigue via electrostimulation
What this could lead to
If successful, this could help design better rehabilitation programs for people with chronic ankle instability.
What could go wrong
This is a small, completed observational study with no treatment being tested, so it won't directly lead to a new therapy. Results may not apply to all patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

72 people

The number who actually took part.

Started

Feb 2023

Finished

Feb 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 44 years

Sex

Male participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Three groups of participants : Chronic ankle instability, lateral ankle sprain copers and healthy controls. INCLUSION CRITERIA: 1. For all three groups : * Physically active male subjects between 18 and 44 years of age * Able to run at low speed. * For homogeneity purposes, the investigators will only recruit subjects who perform a regular physical activity on a weekly basis, including competition participation. 2. Chronic ankle instability : * A history of at least one significant ankle sprain that occurred at least 12 months before study enrolment, associated with inflammatory symptoms, creating at least 1 interrupted day of desired physical activity; * The most recent injury occurred more than 3 months prior to study enrolment; * At least two episodes of giving way in the 6 months prior to study enrolment, recurrent sprain, and/or "feelings of instability"; and * Poor disability status according to the Cumberland Ankle Instability Tool (CAIT) (score ≤ 24/30). 3. Lateral ankle sprain copers : * A history of one significant ankle sprain that occurred at least 12 months before study enrolment, associated with inflammatory symptoms, creating at least 1 interrupted day of desired physical activity; * A return to at least moderate levels of weight-bearing physical activity less than 12 months after initial sprain without recurrent injury, episodes of giving way, and/or feelings of instability; * Minimal, if any, level of self-reported disability (CAIT score ≥ 28/30); and * Minimal, if any, alteration in self-reported function (ADL- and Sport-subscales ≥95%). 4. Healthy controls : * The same inclusion criteria as the LAS coper group, with the exception reported in the exclusion criteria. EXCLUSION CRITERIA: 1. For all three groups : * Being younger than 18 years * Any medical contraindication to physical exertion, * Any systemic or neurological disease, * A recent surgery, * A difference in leg length of more than 3 cm, * Pregnancy, * A body mass index higher than 30kg/m² (due to less accurate motion analysis by absence of anatomical landmarks). * LAS copers and controls will also be excluded if: constant or intermittent ankle pain, ankle fractures, or surgeries, and recent participation in a physical revalidation programme. * Healthy participants must never have suffered an inversion trauma resulting in disability. 2. For healthy controls : the healthy control subjects may not have suffered from an ankle sprain.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • UZ Leuven, Pellenberg

    Lubbeek, B-3212, Belgium

More trials for these conditions

Other studies related to the condition(s) this trial covers.