NCT07105150 Efficacy of a Video-Based Educational Program on Female Urinary Incontinence
| NCT ID | NCT07105150 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Poitiers University Hospital |
| Condition | Urinary Incontinence |
| Study Type | INTERVENTIONAL |
| Enrollment | 144 participants |
| Start Date | 2026-01-09 |
| Primary Completion | 2028-02-15 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 144 participants in total. It began in 2026-01-09 with a primary completion date of 2028-02-15.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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.
Eligibility Criteria
Inclusion Criteria: * Any woman referred for pelvic floor rehabilitation sessions for urinary incontinence (defined as 'any involuntary leakage reported by the patient' according to the International Continence Society) * Women requiring perineal rehabilitation for urinary incontinence * Aged 18 years or older * Having access to a connected device (tablet, smartphone, computer) * Having a functional email address * Covered by a social security scheme * Informed, and written consent (signed by the participant and the investigator) Exclusion Criteria: * Women unable to complete questionnaires (unable to read French or unable to write) * Visually impaired individuals who cannot watch the video or read the printed material * Genital prolapse extending beyond the hymen * Documented neurological disorders * Individuals receiving psychiatric care and those unable to express their consent * History of pelvic fractures or dorsolumbar surgery * Chronic pelvic pain * Women who have given birth within the last 6 month * Individuals with enhanced protection: minors, individuals deprived of liberty, individuals residing in a health or social institution, pregnant or breastfeeding women, adults under legal protection, and patients in emergency situations.
Contact & Investigator
Anne Cecile Pizzoferrato, M.D
STUDY DIRECTOR
University Hospital Center of Poitiers
Frequently Asked Questions
Who can join the NCT07105150 clinical trial?
This trial is open to female participants only, aged 18 Years or older, studying Urinary Incontinence. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07105150 currently recruiting?
Yes, NCT07105150 is actively recruiting participants. Contact the research team at verobmsb@hotmail.com for enrollment information.
Where is the NCT07105150 trial being conducted?
This trial is being conducted at Buxy, France, Chanceaux-sur-Choisille, France, Embrun, France, Hellemmes-Lille, France and 8 additional locations.
Who is sponsoring the NCT07105150 clinical trial?
NCT07105150 is sponsored by Poitiers University Hospital. The principal investigator is Anne Cecile Pizzoferrato, M.D at University Hospital Center of Poitiers. The trial plans to enroll 144 participants.