+1 877 705 191424 / 7
HIPAA Compliant
ISO 27001 Certified

Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
FEMALE
ID07337278

Effect of Lumbopelvic Rehabilitation Using Posturography Combined With 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

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating whether adding lumbopelvic postural rehabilitation to pelvic floor muscle training PFMT improves urinary incontinence symptoms in women compared to PFMT alone. The study focuses on women aged 18 to 65 with urinary incontinence, assessing changes in symptom severity, pelvic floor muscle strength, patient-reported improvement, and quality of life. This clinical trial is randomized and evaluates the effectiveness of combining two rehabilitation approaches in managing urinary incontinence. Participants will be randomly assigned to one of two groups for 12 weeks. The experimental group receives PFMT three times per week along with two weekly sessions of lumbopelvic postural rehabilitation using posturography, which includes stability and mobility exercises for the lumbopelvic area. The control group performs PFMT alone three times per week, including supervised sessions at the hospital and home exercises, focusing on pelvic floor muscle contractions in different positions. During the study, researchers will assess outcomes at the start, 6 weeks, and 12 weeks. Measurements include the International Consultation on Incontinence Questionnaire for urinary incontinence severity, pelvic floor muscle strength, urinary symptom profiles, patient global impression of improvement, and quality of life impact questionnaires. The study includes supervised and home-based training, with monitoring of symptom changes and muscle strength to evaluate treatment effects over the 12-week period.

CONDITIONS

Brief Title

Posturography Rehabilitation and Pelvic Floor Training on Urinary Incontinence in Women

Who Can Participate

Age: 18Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female participants aged between 18 and 65 years
  • Clinical signs of urinary incontinence diagnosed by International Continence Society terminology
  • Urinary Symptom Profile scores for stress urinary incontinence and/or overactive bladder of 1 or higher
  • Normal neuro-perineal examination
  • Provided written informed consent before participation
Not Eligible

You will not qualify if you...

  • Known neurological detrusor overactivity or reduced bladder compliance
  • 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
  • Current urinary tract infection or vaginal infection
  • Cognitive or visual impairments affecting exercise understanding or performance
  • Pregnant women or women within 10 months postpartum
  • Use of anticholinergic medication or hormone replacement therapy in last 6 months
  • Pelvic or abdominal surgery within last 6 months

Research Team

K

Khaoula Mestour

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here