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Tests an electrical stimulation suit in people with spinal cord injury, stroke or amputation

Tests a stimulation suit for nerves, muscles and walking in adults with injury or amputation.

Plain-language title generated from the registry record
Registry title: Effect of Neuro20 Functional Electrical Stimulation Suit on Autonomic Function, Muscle Performance, and Gait

Key facts

Where
Jacksonville and Tampa, United StatesSee the 2 sites

Where in United States

  • Brooks RehabilitationJacksonville, United StatesTaking people
  • The International Institute of Orthotics and ProstheticsTampa, United StatesNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Brooks Rehabilitation
Trial code
NCT07164846
Record updated
19 October 2026
Original description
This research aims to understand the effect of the Neuro20 Functional Electrical Stimulation Suit on autonomic nervous system function, muscle performance, and gait after amputation or neurologic injury.Read full original descriptionShow less

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

This research aims to understand the effect of the Neuro20 Functional Electrical Stimulation Suit on autonomic nervous system function, muscle performance, and gait after amputation or neurologic injury.

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); Active Cancer; Active fever, infection, or acute inflammation; Epilepsy or uncontrolled seizures or seizure within the last 6 months; Bleeding tendency; Implanted medical devices; Active DVT/thrombophlebitis; Pregnancy; 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.

ClinicalTrials.gov NCT07164846