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Efficacy of a Video-Based Educational Program on Female Urinary Incontinence

NCT07105150 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 144

Last updated 2026-02-10

No results posted yet for this study

Summary

The aim of this clinical trial is to assess the effectiveness of a 4-week video-based education program in enhancing urinary continence among women with urinary incontinence referred for pelvic floor rehabilitation

The main question it aims to answer is :

• Does a structured video-based education program reduce the symptoms of urinary incontinence before any pelvic floor muscle strengthening ? Researchers will compare this program to a paper document (providing similar information) to see if this improves urinary continence in women suffering from urinary incontinence.

Participants will :

* receive either the video-based education program or a paper information document (providing similar information) prior to the sessions with the physiotherapist
* then follow pelvic floor rehabilitation sessions with the physiotherapist according to usual practice
* complete the urinary incontinence questionnaire after the 4-week video education program (intervention group) or 4 weeks after receiving the paper document (control group), and after each pelvic floor rehabilitation session with the physiotherapist and at the end of the sessions
* will be monitored at 1 and 2 years to evaluate urinary incontinence following the intervention.

Conditions

Interventions

BEHAVIORAL

video-based education program

The video-based education program will include 4 workshops of 20 minutes each, at a rate of 1 video per week: Video 1: Anatomy and physiology of the pelvic floor; Video 2: Physiology of the urinary tract; Video 3: Physiology of the digestive tract; Video 4: Pathophysiology of urinary incontinence and other pelvic floor disorders (genital prolapse and anal incontinence) and preventive measures in daily activities.

OTHER

written information

The control group will receive a paper information document (containing the same information as the intervention group) during the 4-week period

Sponsors & Collaborators

  • Poitiers University Hospital

    lead OTHER

Principal Investigators

  • Anne Cecile Pizzoferrato, M.D · University Hospital Center of Poitiers

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-09
Primary Completion
2028-02-15
Completion
2030-01-09

Countries

  • France

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07105150 on ClinicalTrials.gov