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Electric suit may loosen stiff muscles in stroke survivors

NCT ID NCT07459361

Symptom relief Sponsor: Hacettepe University Source: ClinicalTrials.gov ↗

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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a special suit that delivers mild electrical pulses can quickly reduce muscle stiffness and improve movement in people who have had a stroke. Twenty-six participants will wear the suit for one hour and be compared to a control group receiving minimal stimulation. Researchers will measure changes in spasticity, walking, and arm function right before and after the session.

What this could mean

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

Active substance
EXOPULSE Mollii Suit (wearable electrical stimulation device)
What this could lead to
If it works, this could point toward a non-drug way to temporarily ease muscle stiffness and improve walking and arm use after a stroke.
What could go wrong
This is a very small, early-stage trial testing only a single session, so any benefits may be short-lived or not apply to all stroke survivors. The control group also gets some stimulation, which may blur results.

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 26 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

Jun 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

18 years and older

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: * Aged 18 years and older * Diagnosed with stroke by a neurologist * Able to walk independently * Presence of spasticity (Modified Ashworth Scale \[MAS\] score \> 1) * Mini-Mental State Examination (MMSE) score of 24 or higher. Exclusion Criteria: * History of recurrent stroke * Difficulty or inability to don and doff the wearable device (e.g., due to severe obesity, mysophobia/hygiene obsession) * Received Botulinum toxin injections or underwent spasticity-related surgery within the past 6 months * Presence of any other neurological or orthopedic conditions (other than stroke) that would prevent participation in the study * Refusal to participate or failure to provide written informed consent.

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Conditions

The condition(s) this trial relates to.

Muscle Spasticity stroke disorder

As listed by the trial registrant

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

Stroke

How to take part

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  1. 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 ↗

  2. A doctor treating you

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