About this trial
Fecal incontinence is a disabling condition that can substantially impair quality of life. This study evaluates whether home-based anal electrical stimulation combined with active voluntary anal sphincter contraction is superior to electrical stimulation alone in patients with fecal incontinence.
The study is a prospective, randomized, parallel-group, open-label controlled trial. Participants will be randomized in a 1:1 ratio to either electrical stimulation with synchronized active sphincter contraction or electrical stimulation alone. The primary outcome is the change in Vaizey/St. Mark's Incontinence Score from baseline to week 12. Secondary outcomes include fecal incontinence episodes, quality of life, anorectal manometry parameters, adherence, safety, and sustained response during follow-up.
Eligibility criteria
Qualifiers
Signed informed consent
Age ≥18 years
Diagnosis of fecal incontinence (urge, passive, or mixed type) with at least 1 episode of involuntary stool leakage requiring hygiene intervention or underwear change per month for ≥3 months
Vaizey (St. Mark's) Incontinence Score ≥8
Disqualifiers
Complete spinal cord injury above the conus medullaris
Active inflammatory bowel disease flare requiring systemic therapy or not in clinical remission
Rectal prolapse requiring surgical intervention
Severe symptomatic hemorrhoids interfering with anorectal assessments or device use
Trial design
Treatments tested in this trial
- Home-based anal electrical stimulator
Treatment groups
Sponsors and collaborators
University Hospital, Martin
Lead sponsor
Comenius University
Collaborator