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

Sponsor
Poitiers University Hospital
Study ID
NCT07105150
Status
Recruiting
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Conditions

  • Urinary Incontinence

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • video-based education program — BEHAVIORAL
    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.
  • written information — OTHER
    The control group will receive a paper information document (containing the same information as the intervention group) during the 4-week period

Study Details

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.

Key Dates

First listed
Aug 5, 2025
Start date
Jan 9, 2026
Status verified
Jan 2026
Primary completion
Feb 15, 2028
Completion
Jan 9, 2030

Study Design

Enrollment
144 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: video-based education program group
  • Active Comparator: written information group

Primary Outcome Measure

Urinary incontinence score comparison between the 2 groups [ Time Frame: At the end of the video-based education program (5 weeks after inclusion) ]

Central Contacts

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