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Completed

NCT Number: NCT06653582

Effect of Postural Reeducation Versus Pelvic Floor Muscle Training on Stress Urinary Incontinence

The purpose of the study is to evaluate the effects of postural reeducation compared to pelvic floor muscle training on urinary incontinence (UI) symptoms, the impact of UI, and quality of life (QoL) in women experiencing stress urinary incontinence (SUI)

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Key information

About this study

The study is designed as a randomized- controlled trial. It will be carried out on women suffering from stress urinary incontinence referred after urology consultations to the Physiotherapy Clinic in Soad Kafafy hospital.

UI, particularly SUI, affects up to 28% of the population and occurs during activities like coughing or sneezing due to inadequate urethral closure pressure. The pelvic floor muscles play a critical role in supporting pelvic organs and maintaining continence. Pelvic floor dysfunction is a significant contributor to SUI. Postural dysfunction can increase mechanical stress and lead to pelvic floor dysfunction. Postural re-education techniques aim to correct imbalances and improve pelvic floor muscle activity, potentially alleviating SUI symptoms by restoring muscle efficiency and enhancing continence.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fifty females with stress urinary incontinence.
  • Age of 30-40 years.
  • Body mass index (BMI) > 30 kg/m2

Exclusion criteria

  • Genital prolapse grade 3 or 4 based on Pelvic Organ Prolapse Quantification Classification (POP-Q).
  • Overactive bladder (OAB)
  • Functional impairment (Barthel scale <85 points).
  • Neurological or cognitive impairment (mini mental examination <24 points).
  • Any other type of urinary incontinence.
  • Pregnancy.
  • History of spinal, hip, knee or foot surgery, pelvic and abdominal surgery (including cesarean section)
  • Smoking, chronic cough, history of respiratory diseases, osteoporosis (self-reported).

Treatment and study plan

Postural reeducation

Other

The program will include postural awareness, stretching, McKenzie's method, and manual therapy for 12 weeks.

Pelvic floor exercises

Other

The program will include pelvic floor exercises for 12 weeks. Three sets of 10 long contractions will be performed, each sustained for 6-8 seconds, three times a day. After each contraction, participants will be asked to rest for the same period. Two series of 10 fast contractions will be recommended, consisting of short, quick exercises of 1- to 2-second contractions, followed by long, sustained exercises lasting 5-10 seconds.

Primary outcomes

  1. Urinary incontinence (UI) symptoms

    Time frame: 12 weeks

    UI symptoms will be measured using a 48-hour Pad Test [14]. This is a standardized test for assessing urine leakage that can be performed at home[15]. Women replace pads as needed over the course of 48 hours. The results are calculated by subtracting the net weight of used pads from the total weight of non-used pads. The Pad Test results can be classified as mild (4-20 g), moderate (21-74 g), or severe UI (> 75 g).

  2. Urinary incontinence (UI) impact

    Time frame: 12 weeks

    It will be assessed using the International Consultation Incontinence Short-Form (ICIQ-UI-SF). UI impact will be derived from the values of the third question assessing overall impact ("How much does leaking urine interfere with everyday life?", ranging from 0 to 10), with a higher score indicating a greater UI impact.

Secondary outcomes

  1. Urinary incontinence-Quality of life (UI-QoL)

    Time frame: 12 weeks

    It will be assessed using the International Consultation Incontinence Short-Form (ICIQ-UI-SF). The UI-QoL will be calculated using the questionnaire's final score (range from 0 to 21), which is the total of the three items, with a higher score indicating more severe UI and a bigger influence on QoL.

Sponsors and collaborators

Lead sponsor

Misr University for Science and Technology

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 22, 2024
Registry last updated
Feb 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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