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Treatment of Fecal Incontinence and Functional Evacuation Disorders Using Non-instrumental Biofeedback

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Re-verified, no change to tracked fieldsv5
  2. Notable Primary completion date: Apr 28, 2025 to Apr 30, 2026
    • Study completion date: Dec 31, 2025 to Aug 30, 2026
    • Start date: Apr 19, 2024 to Apr 17, 2024
    • Study title revised
    v4
  3. Minor Secondary endpoints: details revised at 3 of 9 entriesv3
  4. Notable Start date: Feb 1, 2024 to Apr 19, 2024
    • Primary completion date: Feb 28, 2025 to Apr 28, 2025
    • Secondary endpoints: details revised at 1 of 9 entries
    v2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Background. Rehabilitation and re-education using instrumental anorectal biofeedback are the main treatment of anorectal functional disorders producing incontinence and outlet obstructed defecation. These treatments imply intubation of patient and several sessions of treatment leading to high consumption of resources and costs. Hypothesis. A cognitive intervention based on original audiovisual programs developed specifically for the management of anorectal functional disorders is effective in correcting anorectal function disorders that cause fecal incontinence and evacuation disorders. Aim. To prove in two different protocols (fecal incontinence and dyssinergic defecation) the efficacy of specifically developed non-instrumental biofeedback techniques. Selection criteria. Patients with fecal incontinence and altered sphincter function and patients with outlet obstructed evacuation referred for biofeedback treatment. Intervention. In separate studies (incontinence and dyssynergic defecation) patients will be randomized into biofeedback and placebo groups. One session of either biofeedback or placebo intervention will be performed at the beginning of the intervention period and patients will be instructed to performed the assigned daily treatment at home. A visit for outcome assessment will be performed at 3 months in incontinence study and at 4 weeks in the dyssinergic defecation study. In addition, in the incontinence study a phone call will be performed after 6 months of the beginning of the study to evaluate treatment outcome. Biofeedback: patients will be taught to control anal and abdominal muscular activity by providing instructions using original video supports. Patients will be instructed to perform the same exercises daily at home in scheduled times. Placebo: a pill of placebo containing 0.3 g glucose will be administered every day at home.
Trial Details
NCT Number NCT06273046
Lead Sponsor Hospital Universitari Vall d'Hebron Research Institute
Conditions
(from sponsor)
Fecal Incontinence, Outlet Dysfunction Constipation
Related terms Fecal Incontinence
Enrollment 96 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov