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Brain-Powered rehab: robot reads mind and muscles to restore hand movement after stroke

NCT ID NCT07737431

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 30, 2026 · Last updated Aug 04, 2026 · Updated 3 times

Summary

This trial tests whether a wrist-hand rehabilitation robot that uses both brain and muscle signals can help people with chronic stroke recover better than one using muscle signals alone. Forty-eight participants will receive 20 training sessions with the robot, which provides electrical stimulation and robotic assistance. The study measures improvements in motor function and brain-muscle coordination up to three months after training.

What this could mean

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

Active substance
a closed-loop sensorimotor integrated exoneuromusculoskeleton (ENMS) that uses both brain and muscle signals to trigger electrical stimulation and robotic assistance for wrist-hand rehabilitation
What this could lead to
If it works, this approach could lead to more effective, personalized rehabilitation for people with chronic stroke, improving hand and wrist function beyond current muscle-only methods.
What could go wrong
This is a small, early-stage trial with only 48 participants, so results may not apply to everyone. The technology is complex and may not work for all levels of impairment.

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

About 48 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2025

Expected to finish

Dec 2027

An estimate. End dates often move.

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

30 to 70 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: 1. at least 6 months after the onset of a unilateral lesion due to stroke; 2. moderate to severe motor disability in the paretic wrist-hand joints (6\<Fugl-Meyer Wrist-Hand Assessment (FMAWH)\<14) and spasticity in wrist-hand (Modified Ashworth Score (MAS) ≤3); 3. sensory impairment on their affected forearm with a score of 1 measured by the sensation part of light touch in the FMA; 4. maximal voluntary contraction (MVC) with detectable EMG (3 times of the standard deviation above the resting EMG baseline) in the muscle union of the flexor digitorum and flexor carpi radialis (FD-FCR) and that of the extensor digitorum and extensor carpi ulnaris (ED-ECU); 5. sufficient cognition to follow experimental instructions (Mini-Mental State Examination score \>21); 6. aged from 30 to 70 years. Exclusion Criteria: 1. currently pregnant; 2. dysphasia (language deficiency); 3. skull implantation; 4. post-stroke neglect; 5. pacemaker implantation; 6. involved in drug studies, other clinical trials, or concurrent medication/occupational/physical treatments on the upper limb; 7. the overall medical condition not suitable for the training (e.g., severe cardiac problem, unstable blood pressure, etc.).

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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.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • The Hong Kong Polytechnic University

    RECRUITING

    Hung Hom, Kowloon, Hong Kong

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