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Study identifier: NCT06273046 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Fecal Incontinence · Outlet Dysfunction Constipation  ·  Sponsor: Hospital Universitari Vall d'Hebron Research Institute

PhaseNA
Planned participants96
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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…

This description comes directly from the study's public registry record.

Talk to the study team

Jordi Serra, MD  ·  34 932746259  ·  jordi.serra@vallhebron.cat

Gloria Santaliestra  ·  gloria.santaliestra@vhir.org

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Vall d'HebronBarcelona, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06273046