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Powered arm brace could give SCI patients a helping hand

NCT ID NCT06349434

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests whether a powered arm brace called MyoPro can help people with incomplete spinal cord injury improve arm and hand function. Sixty adults aged 18-80 with specific injury levels will either use the device or receive standard therapy. Researchers will measure strength, range of motion, and daily living skills over time.

What this could mean

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

Active substance
MyoPro powered arm brace
What this could lead to
If it works, this could provide a practical way for people with spinal cord injury to improve arm and hand function in daily life.
What could go wrong
This is an early-stage study with only 60 people, so results may not apply to everyone. The device may be cumbersome or not help enough to justify regular use.

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 60 people

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

Started

Oct 2023

Expected to finish

Oct 2028

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 to 80 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: * Be between ages 18-80 * Be able to activate certain muscles in my arm and forearm on my own a sufficient amount as measured by EMG amplitude. This will be determined by the study OT/PT. * Be diagnosed with spinal cord injury (SCI) with level C1-C8 and ASIA Impairment Scale (AIS) C or D, as determined by study staff. If I have not had an exam to determine my injury level and impairment scale recently, I may participate in an examination of my sensation and strength in my arms, legs, trunk and rectum as was done in the hospital soon after my injury. * Be at least 1-year post injury * Have sufficient ability to move my shoulder (active shoulder flexion of 30 degrees and active shoulder abduction 20 degrees), as determined by study staff * Be medically stable * Have sufficient learning and memory abilities and abilities to communicate in English to be able to participate and follow directions during my rehabilitation * Continue to take all prescribed medication (e.g., oral or via pump baclofen) without any dosing changes * Be able to tolerate functional tasks for 60 minutes with periodic rests without excessive fatigue * Have minimal strength in the muscles that bend and straighten my elbow, as determined by study staff * Have full range of motion in my elbow when it is moved by the study therapist Exclusion Criteria: * Be younger than 18 years old or older than 80 * Have excessive pain in my arm, wrist, or hand that limits providing rehabilitation * Have excessive spasticity in my elbow or wrist, as determined by study staff * Be participating in any experimental rehabilitation or drug studies * Have history of nervous system disorder other than SCI * Have difficulty following multiple step directions * Have severe cognitive or psychiatric problems might be contraindications to start training. * Have skin issues or severe sensory deficits that would prevent wearing the Myo-Pro device safely * Be pregnant * Have other conditions or circumstances that, in the opinion of the investigators, would affect the safety or effectiveness of the training in which I would participate

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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

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Kessler Foundation

    RECRUITING

    West Orange, New Jersey, 07052, United States

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