Clinical trial Recruiting at 1 site Interventional Ages 18 to 65 Women only

Preoperative pelvic floor muscle training for women with urinary incontinence

Official title: Investigation of the Preoperative Effectiveness of Intensive Pelvic Floor Muscle Training in Women With Urinary Incontinence: a Randomized Controlled Trial.

Run by Gulhane School of Medicine · NCT06957795 · Data updated 2026-11-12

This study tests whether a special exercise program for pelvic floor muscles can help women with urinary incontinence feel better before they have surgery.

More Urinary Incontinence (UI) trials

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexWomen only
Enrollment60 (estimated)
SponsorGulhane School of Medicine
Academic / other
Locations1 site (Ankara)
StatusRecruiting
StartedJanuary 1, 2025
Main results expectedJune 1, 2025
Study endsSeptember 1, 2025
Registry record updatedMay 8, 2025
Trial IDNCT06957795 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are women aged 18-65 diagnosed with SUI or SUI-predominant mixed type urinary incontinence.

Probably not a fit

Patients who may not benefit include those who are pregnant, have had previous pelvic floor surgery, or have certain medical conditions affecting muscle function.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of an intensive pelvic floor muscle training program for women diagnosed with stress urinary incontinence (SUI) before undergoing surgery. The program aims to strengthen pelvic floor muscles, which support pelvic organs and help alleviate symptoms of urinary incontinence. Participants will be women aged 18-65 who have been referred for physiotherapy and can actively contract their pelvic floor muscles. The study will assess compliance with the exercise regimen and its impact on urinary incontinence symptoms prior to surgical intervention.

Why it matters

Potential benefit: If successful, this approach could significantly improve urinary incontinence symptoms in women, potentially reducing the need for surgical interventions.

How similar studies have gone: Other studies have shown positive outcomes with pelvic floor muscle training for urinary incontinence, indicating that this approach is supported by existing evidence.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria for the study:

* Being a woman between the ages of 18-65
* Being diagnosed with SUI or SUI-predominant mixed type urinary incontinence by an obstetrician-gynecologist
* Having active pelvic floor muscle contraction
* No genital anatomical abnormality
* Being able to understand and follow verbal and written instructions
* The patient was referred to physiotherapy at least 6 weeks before the planned surgery date
* Patients performed 75% or more of the given exercises (categorized as adequate compliance)

Exclusion criteria for the study:

* Not volunteering to participate
* Being pregnant
* Having had previous pelvic floor surgery
* Having received previous pelvic floor physiotherapy
* Having a vaginal or urinary infection
* Being unable to tolerate pelvic floor muscle function measurement
* Having a neuromuscular or neurological disease that may affect muscle function

Where it's running

  • Gülhane Education and Research Hospital, Department of Obstetrics and Gynecology
    Ankara, Turkey (Türkiye)
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.