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Neuro20 Functional Electrical Stimulation Suit for Spinal Cord Injury, Stroke, and Amputees

This study is looking at how the Neuro20 Functional Electrical Stimulation Suit affects your body's automatic functions (like heart rate and breathing), muscle strength, and walking ability after a spinal cord injury, stroke, or amputation. The Neuro20 suit uses electrical stimulation to help your muscles work better. We want to see if using this suit can improve how you walk. You might be able to join if you are at least one week past your injury or amputation, are medically stable, and can understand and follow simple instructions. The study aims to enroll 30 participants, but the current recruitment status is unclear.

Study design
This is an interventional study planning to enroll 30 participants. It is not specified if it is randomized or blinded.
What's involved
You will complete up to 12 therapy sessions, each lasting 1-2 hours. During each session, you will wear the Neuro20 suit and receive up to 105 minutes of electrical stimulation.
Compensation
Not stated in the trial record.
Follow-up
Your gait will be measured before the intervention, at 1 week (mid-intervention), and at 4 weeks (post-intervention).

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07164846

Effect of Neuro20 Functional Electrical Stimulation Suit on Autonomic Function, Muscle Performance, and Gait

Recruiting
NAAges 18+InterventionalTreatment
Brooks Rehabilitation
~30 participants
Updated 2025-10-31 on ClinicalTrials.gov
What's tested:Therapy Sessions

At a glance

Recruiting sites
1 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in Gait
Measured over Pre-intervention, mid-intervention at 1 week, and post-intervention at 4 weeks

Conditions

Spinal Cord Injury
Stroke
Amputees

Explore related trials

AmputationBrain InjurySpinal Cord InjuryStroke

Where it's being run

2 sites across 1 states
Florida2

Study leadership

  • Mark Bowden, PT, PhD · PRINCIPAL_INVESTIGATOR · Brooks Rehabilitation

Who to contact

Hannah Grimes
[email protected]
904-597-3478
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

At least one week post amputation or neurologic injury (i.e. brain injury, stroke, spinal cord injury) and deemed medically stable to participate in rehabilitation
Able to provide Informed Consent by demonstrating the ability to follow a three step command

Exclusion

Pacemaker / Defibrillator or severe cardiac disease (Class IV according to New York Heart Association Functional Classification)
Implanted medical devices
Active DVT/thrombophlebitis
Active Cancer
Active fever, infection, or acute inflammation
Pregnancy
Epilepsy or uncontrolled seizures or seizure within the last 6 months
Implanted stimulator or pump that cannot be turned off externally
Significant, active wounds in areas stimulated by the suit
Inability to follow a three-step motor command
Bleeding tendency

What this trial measures

  • Change in GaitPre-intervention, mid-intervention at 1 week, and post-intervention at 4 weeks

    The 6-minute walk test is a simple, standardized test used to assess a person's exercise capacity and functional mobility. An increase in distance walked reflects an improvement in mobility and gait.