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Say 'Bend Arm' to recover: Voice-Activated robot may boost stroke rehab

NCT ID NCT07398131

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests whether using voice commands to control a robotic arm exoskeleton can improve upper limb recovery in stroke survivors. 32 participants will either use a voice-triggered robot (by saying commands like 'bend arm' while imagining the movement) or receive standard passive robot therapy. The goal is to see if the active, voice-driven approach leads to better arm function and brain-to-muscle signal recovery.

What this could mean

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

Active substance
single-joint robot (Active Voice-Controlled Mode)
What this could lead to
If it works, this could point toward a more engaging and effective way to regain arm function after a stroke.
What could go wrong
This is a small, early-stage study with only 32 participants, so results may not apply to everyone. The improvement over standard therapy may be small or none.

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 32 people

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

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

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

20 to 85 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: * Ischemic or hemorrhagic stroke diagnosed by CT or MRI * Stroke onset occurred at least 1 month prior to enrollment * Aged 20 to 80 years * Moderate to severe upper limb impairment (Fugl-Meyer Assessment-Upper Extremity score between 13 and 47) * Cognitive function sufficient to follow instructions (MMSE score \> 20) * Stable medical condition with no severe pain in the affected upper limb Exclusion Criteria: * Severe spasticity of the affected upper limb (Modified Ashworth Scale score \> 2) * History of other neurological diseases (e.g., Parkinson's disease, brain tumor) * Serious orthopedic conditions or skin lesions on the affected upper limb that prevent robot use * Unstable epilepsy or severe psychiatric disorders * Pregnancy

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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

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  1. The official record

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