Pelvic Floor Rehabilitation Study (Beckenboden-Rehabilitationsstudie - BREST)
Not Applicable
Completed
- Conditions
- Postpartum Urinary Incontinence
- Registration Number
- NCT06031870
- Lead Sponsor
- Medical University of Vienna
- Brief Summary
This study compares the effectiveness of standard care, pelvic floor muscle training or vaginal pessary for the treatment of postpartum urinary incontinence.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 52
Inclusion Criteria
- 18 years or older
- gave birth within the 12 weeks prior to the postpartum visit
- postpartum urinary incontinence
- able to understand and give consent in German
Exclusion Criteria
- treatment for postpartum urinary incontinence that started prior to inclusion
- any neurologic disease that impairs bladder function
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method patients' self-reported satisfaction with the treatment 12 weeks
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie postpartum urinary incontinence pathophysiology and pelvic floor dysfunction?
How does pelvic floor muscle training compare to vaginal pessary in managing postpartum stress urinary incontinence?
Which biomarkers correlate with response to pelvic floor rehabilitation in postpartum women with urodynamic stress incontinence?
What are the long-term adverse events associated with vaginal pessary use for postpartum incontinence management?
Are there combination therapies involving pelvic floor exercises and neuromodulation devices for postpartum urinary incontinence?
Trial Locations
- Locations (1)
Die GynPraxis
🇩🇪Mainz, Germany
Die GynPraxis🇩🇪Mainz, Germany