Actively Recruiting
Posturography Rehabilitation and Pelvic Floor Training on Urinary Incontinence in Women
Led by Mohammed V University in Rabat · Updated on 2026-01-13
78
Participants Needed
1
Research Sites
14 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to evaluate whether lumbopelvic postural rehabilitation combined with pelvic floor muscle training (PFMT) is more effective than PFMT alone in women with urinary incontinence. The main questions it aims to answer are: * Does the addition of lumbopelvic postural rehabilitation improve the severity of urinary incontinence as measured by the ICIQ-UI-SF questionnaire? * Does it improve urinary symptom profile, pelvic floor muscle strength, patient-reported overall improvement, and quality of life compared to PFMT alone? Participants will be randomly assigned to one of two groups: * Experimental group (Group A): PFMT (3 sessions/week) plus lumbopelvic postural rehabilitation (2 sessions/week) for 12 weeks. * Control group (Group B): PFMT alone (3 sessions/week) for 12 weeks. Participants will perform pelvic floor exercises in supine and seated positions, with supervised sessions at the hospital and home exercises. Postural rehabilitation includes stability and mobility exercises for the lumbopelvic region using Posturography. Outcomes will be assessed at baseline, at 6 weeks, and at 12 weeks.
CONDITIONS
Official Title
Posturography Rehabilitation and Pelvic Floor Training on Urinary Incontinence in Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female participants aged between 18 and 65 years
- Clinical signs of urinary incontinence (stress, urge, or mixed) diagnosed by International Continence Society terminology
- Urinary Symptom Profile scores for stress urinary incontinence and/or overactive bladder of at least 1
- Normal neuro-perineal examination
- Written informed consent provided before participation
You will not qualify if you...
- Known detrusor overactivity or reduced bladder compliance due to neurological causes
- Voiding dysfunction with Urinary Symptom Profile dysuria subscale score of 1 or higher
- Organic or morphological pathology of the lower urinary tract
- Pelvic organ prolapse grade II or higher based on POP-Q system
- Current urinary tract or vaginal infection
- Cognitive or visual impairments affecting ability to understand or perform exercises
- Pregnant or within 10 months post childbirth
- Use of anticholinergic medication or hormone replacement therapy within last 6 months
- Pelvic or abdominal surgery within past 6 months
AI-Screening
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Trial Site Locations
Total: 1 location
1
Al Ayachi Hospital, CHU Ibn Sina
Rabat, Rabat-Salé-Kénitra, Morocco, 10000
Actively Recruiting
Research Team
K
Khaoula Mestour
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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