Utility of an Animated Bowel Biofeedback Training Routine to Improve Bowel Function in Individuals With SCI
Spinal Cord Injury, Constipation, Fecal Incontinence
About this trial
This is an interventional treatment trial for Spinal Cord Injury focused on measuring Spinal Cord Injury, Constipation, Fecal Incontinence, Neurogenic Bowel, Bowel Biofeedback, Manometry
Eligibility Criteria
Inclusion Criteria:
- Chronic SCI (duration over 1 year)
- Able-bodied (no SCI)
Exclusion Criteria:
- Contraindication to bowel biofeedback
- Currently pregnant or trying to become pregnant
- Inability to provide informed consent
Sites / Locations
- James J. Peters VA Medical Center, Bronx, NY
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Anorectal Manometry
Bowel Biofeedback Training
Part 1 [Anorectal Manometry]: Fifty SCI subjects and 15 AB subjects will undergo anorectal manometry and a baseline assessment of level of constipation or frequency of fecal incontinence (FI). Additional 10 able-bodied subjects will be enrolled to serve as controls. The 10 Question Bowel Survey and Incontinence Scale will be administered.
Part 2 [Bowel Biofeedback]: A subgroup of 20 subjects who participated in the first arm of the study (Anorectal Motility) and report either constipation or fecal incontinence will be asked to participate in 12 weeks of twice weekly, biofeedback training. The biofeedback training will consist of in-lab exercises that are paired with a visual feedback. Anorectal manometry and bowel surveys will be repeated after the training session to assess the effects of bowel biofeedback on anorectal function.