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Magnetic pulse therapy shows promise for wobbly ankles

NCT ID NCT05500885

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether adding pulsed electromagnetic field (PEMF) therapy to standard rehab helps people with chronic ankle instability. 62 adults with a history of ankle sprains and ongoing instability received either real PEMF or a sham device alongside rehab. The goal was to see if PEMF reduces pain, improves balance, and strengthens ankle muscles.

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

62 people

The number who actually took part.

Started

Jan 2023

Finished

Jan 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 70 years

Sex

Anyone

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.

* Inclusion in the CAI stratum: * Requires a history of at least one significant sprain \> 12 months prior to consent * Continued perceived or episodic "giving way" of the ankle * Reported Cumberland Ankle Instability Tool (CAIT score \< 24) Exclusion Criteria for CAI: * A history of surgeries or fractures of either lower extremity limbs * Concomitant lower extremity pathology, e.g. vascular disease and osteoarthritis * Inadequate muscle strength in lower limb which require ambulation support (e.g., crutches) or any vestibular or balance disorders * Pregnancy * Cognitive impairment/Neurological conditions, and neurological disorders (e.g. dementia) -Concussion within the last 6 months * Bilateral instability condition * Regular use of medicine or antibiotics * Metal implantation in their body * Unable to walk at enrolment * Non-removable cast

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Prince of Wales Hospital

    Hong Kong, Hong Kong, New Territories, Hong Kong

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