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Tests treatment safety and results for Urinary Incontinence
Official title Efficacy of a Video-Based Educational Program on Female Urinary Incontinence
ClinicalTrials.gov ID: NCT07105150
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only
You may be able to join if
- Any woman referred for pelvic floor rehabilitation sessions for urinary incontinence (defined as 'any involuntary leakage reported by the patient'...
- 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
You likely can't join if
- 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
See the full eligibility 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)
- 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...
The study team makes the final eligibility decision.
Where it's taking place
- Buxy, France
- Chanceaux-sur-Choisille, France
- Embrun, France
- Hellemmes-Lille, France
- La Roche-sur-Yon, France
- Montignac, France
- Montigny-lès-Metz, France
- Paris, France
- Saint-Jean-de-Braye, France
- Saint-Médard-en-Jalles, France
- Villejuif, France
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Buxy, France; Chanceaux-sur-Choisille, France; Embrun, France; Hellemmes-Lille, France; La Roche-sur-Yon, France; Montignac, France and 5 more location(s). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.