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Can hand exercises and electrical stimulation ease MS sensory problems?

NCT ID NCT01866878

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
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a rehabilitation program for hand sensitivity problems in people with multiple sclerosis. The program used TENS (a mild electrical stimulation device) and hand exercises to improve the ability to feel and recognize objects. The goal was to improve quality of life and hand function. Only 10 participants were planned, and the study was terminated early.

What this could mean

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

Active substance
TENS (transcutaneous electrical nerve stimulation) device and sensory rehabilitation exercises
What this could lead to
If successful, this approach could offer a way to improve hand sensation and daily function for people with multiple sclerosis.
What could go wrong
This was a very small, early-stage trial that was terminated, so results are limited. The benefits of TENS for sensory issues in MS are not well proven.

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

10 people

The number who actually took part.

Started

Jul 2013

Finished

Jul 2015

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: * Patients with relapsing remitting MS defined according to Poser criteria \[9\] and McDonald \[5\]. * Age ≥ 18 years, male or female sex * Patients with sensory disorders interesting hands, evidenced by clinical examination objective. * Patients with an EDSS between 2 and 4 with functional sensitivity parameter ≥ 2. * Patients affiliated to a social security scheme. * Patients signed informed consent for the study. Exclusion Criteria: * Patients with other central or peripheral disorders may affect the sensitivity of the hand. * Patients with allodynia in the study area * Patients with a motor and / or deficit cerebellar ataxia of the upper limbs. * Patients treated with psychotropic or antiepileptic drugs. * Patients for whom a flare occurred affecting the sensitivity of the hand, within 30 days before enrollment. * Patients holders of an active implantable medical device. * Pregnant women and vulnerable patient population.

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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

  • Hôpital Pasteur

    Nice, 06000, France

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