Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05745298

The Use of Functional Electrical Stimulation in Conjunction With Respiratory Muscle Training to Improve Unaided Cough in Individuals With Acute Spinal Cord Injury

Led by University of Miami · Updated on 2025-07-09

50

Participants Needed

1

Research Sites

217 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The overall objective of this study is to improve unaided cough with abdominal and latissimus dorsi functional electrical stimulation in conjunction with respiratory muscle training in individuals with acute spinal cord injuries.

CONDITIONS

Official Title

The Use of Functional Electrical Stimulation in Conjunction With Respiratory Muscle Training to Improve Unaided Cough in Individuals With Acute Spinal Cord Injury

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Traumatic and atraumatic C2-T12 spinal cord injury (AIS A, B, and C motor incomplete and complete injuries) admitted to inpatient rehabilitation with injury date less than 12 months prior to enrollment
  • Positive response to electrical stimulation through a palpable contraction
  • Fluent in written and spoken English
Not Eligible

You will not qualify if you...

  • Individuals who do not meet inclusion criteria
  • Prisoners
  • Concurrent traumatic brain injury with Rancho level of cognitive functioning less than VI
  • Individuals with open tracheostomy
  • Persons with pacemakers
  • Pregnant women
  • Persons with epilepsy
  • Open wounds or metal implants at site of electrode placement
  • Unresponsive to functional electrical stimulation
  • Current diagnosis or history of thoraco-abdomino-pelvic cancer

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Miami

Miami, Florida, United States, 33136

Actively Recruiting

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Research Team

G

Gary J Farkas, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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