Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06273046

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

Led by Hospital Universitari Vall d'Hebron Research Institute · Updated on 2025-07-06

96

Participants Needed

1

Research Sites

123 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged between 18 and 75 years
  • For incontinence studies: at least 4 episodes of fecal incontinence in the last 14 days
  • For dyssynergic defecation studies: constipation with less than 3 complete spontaneous bowel movements per week and/or Bristol type 1 or 2 stools in more than 25% of bowel movements in the prior 2 weeks
  • Ability to follow instructions and attend study visits
Not Eligible

You will not qualify if you...

  • Presence of organic digestive diseases such as inflammatory bowel disease, celiac disease, or gastro-duodenal ulcer
  • Neurological diseases including spinal cord injury, multiple sclerosis, or Parkinson's disease
  • Previous or active colon and/or rectal cancer
  • Rectal fistula
  • Rectal prolapse
  • Total colectomy
  • Any radiation to the pelvis in the last month

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hospital Vall d'Hebron

Barcelona, Spain

Actively Recruiting

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Research Team

J

Jordi Serra, MD

CONTACT

G

Gloria Santaliestra

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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