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Shock and roll: new combo therapy aims to reboot Stroke-Damaged arms

NCT ID NCT07112911

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study is testing whether combining two types of electrical stimulation with a robotic arm trainer can help people who had a stroke at least six months ago improve their arm movement. 65 participants will receive 20 sessions over 4-7 weeks. The goal is to see if this approach can improve motor function and reduce muscle stiffness.

What this could mean

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

Active substance
Electrical stimulation (trans-spinal and neuromuscular) combined with a rehabilitation robot
What this could lead to
If it works, this could point toward a more effective way to restore arm movement after a stroke, improving daily life for survivors.
What could go wrong
This is a small, early-stage study with no control group, so results may not be conclusive. The therapy is intensive and may not work for everyone.

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 65 people

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

Started

Jul 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

25 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: * Subjects in the chronic stage (start from 6 months after the onset of stroke) with a pure unilateral motor paresis after a stroke (ischemic or hemorrhagic); * Sufficient cognition to follow simple instructions as well as understand the content and purpose of the experiment (Mini-Mental State Examination (MMSE) score\>23); * Be able to sit up for 60 minutes (with or without assistance); * Muscle strength graded from 1 to 3 in biceps brachii, triceps brachii, extensor carpi radialis, flexor carpi radialis, and abductor pollicis brevis in the affected side. * The voluntary electromyographic signals of the wrist extensor and wrist flexor muscle groups can be detected. Exclusion Criteria: * Patients with secondary stroke; * Severe dysphasia (either expressive or comprehensive) with inadequate communication; * Any additional medical or psychological condition affecting their ability to comply with the study protocol; * History of other neurological disease, psychiatric disorder, including alcoholism and substance abuse; * currently pregnant; * epilepsy; * pacemaker implantation or deep brain stimulation; * involved in drug studies, other clinical trials, or concurrent medication/occupational/physical treatments on the upper limb; * skin disease at the area of the electrodes; * High hypertension and cannot maintain normal blood pressure despite daily intake of antihypertensive medication.

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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

    2 sites. 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.

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  3. A doctor treating you

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Contacts and locations

Locations

  • The Hong Kong Polytechnic University

    RECRUITING

    Hong Kong, Hong Kong

  • The Hong Kong Polytechnic University

    RECRUITING

    Hong Kong, Hong Kong

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