RECRUITING

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

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2025-08-05

Study Completion:2026-08-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT07164846

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* 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	* 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

Inclusion Criteria

Exclusion Criteria

* 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

* 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

Contacts and Locations

Study Contact

Hannah Grimes

CONTACT

904-597-3478

hannah.grimes@brooksrehab.org

Principal Investigator

Mark Bowden, PT, PhD

PRINCIPAL_INVESTIGATOR

Brooks Rehabilitation

Study Locations (Sites)

Brooks Rehabilitation

Jacksonville, Florida, 32216

United States

The International Institute of Orthotics and Prosthetics

Tampa, Florida, 33634

United States

Collaborators and Investigators

Sponsor: Brooks Rehabilitation

Mark Bowden, PT, PhD, PRINCIPAL_INVESTIGATOR, Brooks Rehabilitation

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-08-05

Study Completion Date2026-08-01

Study Record Updates

Study Start Date2025-08-05

Study Completion Date2026-08-01

Terms related to this study

Additional Relevant MeSH Terms

Spinal Cord Injury
Stroke
Amputees