RECRUITING

At-Home Genital Nerve Stimulation for SCI Bowel

Description

The purpose of this study is to test whether electrical stimulation of the skin in the pelvic area (near the genitals) can reduce the reflexes that cause bowel accidents in people with spinal cord injuries. Current bowel treatments either involve diet and medications or surgery. This study will evaluate whether electrical stimulation can be an alternate option for bowel management. Researchers will: * Use an FDA approved Transcutaneous Electrical Nerve Stimulation (TENS) device off-label * Compare a target stimulation level to a placebo stimulation level Participants will: * Use electrical stimulation on the skin in the pelvic area for 6-8 hours each day for 4 weeks at home * Visit the research center 3 times to participate in exams and answer questions * Keep a daily diary of their bowel symptoms and stimulation times

Conditions

Spinal Cord Injury
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Related Conditions:

Spinal Cord Injury

Study Overview

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Study Details

Study overview

The purpose of this study is to test whether electrical stimulation of the skin in the pelvic area (near the genitals) can reduce the reflexes that cause bowel accidents in people with spinal cord injuries. Current bowel treatments either involve diet and medications or surgery. This study will evaluate whether electrical stimulation can be an alternate option for bowel management. Researchers will: * Use an FDA approved Transcutaneous Electrical Nerve Stimulation (TENS) device off-label * Compare a target stimulation level to a placebo stimulation level Participants will: * Use electrical stimulation on the skin in the pelvic area for 6-8 hours each day for 4 weeks at home * Visit the research center 3 times to participate in exams and answer questions * Keep a daily diary of their bowel symptoms and stimulation times

At-Home Feasibility Trial of Genital Nerve Stimulation to Modulate Neurogenic Bowel Dysfunction in Individuals Living With Spinal Cord Injury

At-Home Genital Nerve Stimulation for SCI Bowel

Condition
Spinal Cord Injury
Intervention / Treatment

-

Contacts and Locations

Cleveland

MetroHealth Center for Rehabilitation Research, Cleveland, Ohio, United States, 44109

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Traumatic SCI.
  • 2. Minimum of 6 months' post-injury.
  • 3. Aged 18 years and older.
  • 4. Neurological level of injury T12 or higher and AIS grade A-D, as defined by the ISNCSCI.
  • 5. Score of 14 or higher on the ISCI BF BDS v2.1.
  • 6. Response to genital nerve stimulation able to be elicited upon screening.
  • 7. Able to understand and provide informed consent.
  • 1. Currently enrolled in another functional electrical stimulation (FES) research trial.
  • 2. Females who are pregnant or planning to become pregnant in the duration of the trial (identified by self-report).
  • 3. Presence of a cardiac pacemaker, implanted defibrillator, or other implanted functional electrical stimulation device if, upon clinical evaluation, it may have an interaction with GNS.
  • 4. In the judgment of the PI and Co-Investigators, presence of medical complications that may interfere with the execution of the study.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

MetroHealth Medical Center,

Kim Anderson, PhD, PRINCIPAL_INVESTIGATOR, MetroHealth System, Ohio

Study Record Dates

2026-09-30