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Stroke rehab gets a High-Tech boost: biofeedback training cuts fall risk

NCT ID NCT07448948

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tested whether adding a special balance-training device to standard rehab helps people who had a stroke at least six months ago. The device uses a platform that gives real-time visual feedback as the person shifts their weight. Thirty-six participants were split into two groups: one got standard rehab alone, the other got standard rehab plus 25 minutes of biofeedback training five days a week for eight weeks. Researchers measured balance, fall risk, daily independence, and emotional well-being before and after the program.

What this could mean

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

Active substance
biofeedback-based interactive posturographic balance training device
What this could lead to
If effective, this approach could become a standard addition to stroke rehabilitation to improve balance and reduce falls.
What could go wrong
This is a small, completed trial with only 36 participants, so results may not apply to all stroke survivors. The device is not a cure and only targets symptom improvement.

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

36 people

The number who actually took part.

Started

Feb 2021

Finished

Oct 2021

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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 Criteria: * At least 6 months had elapsed since stroke onset * They were ambulatory prior to stroke * They were able to stand independently for at least 2 minutes * Mini-Mental State Examination (MMSE) score ≥22 Exclusion Criteria: * Medical conditions contraindicating participation in an exercise program * Additional disorders affecting balance assessment (vertebrobasilar or peripheral vestibular insufficiency, significant visual impairment, neglect, cognitive impairment, major lower extremity contracture, neuromuscular disease, other neurological pathology, impaired joint position sense) * Previous history of stroke * Cerebellar involvement (dysmetria, dysdiadochokinesia, ataxia)

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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

  • University of Health Sciences, Istanbul, Turkey

    Istanbul, Istanbul, 34147, Turkey (Türkiye)

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