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Active, Not Recruiting

NCT Number: NCT07537309

Effects of Diaphragmatic Breathing With Kegal Exercises on Pelvic Floor Muscle Function and Quality of Life Among Multigravida Women With Stress Incontinence

The goal of this clinical trial is to determine the effect of diaphragmatic breathing with kegel exercises on pelvic floor muscle function and quality of life among multigravida women with stress urinary incontinence The main question it aims to answer are The effect of diaphragmatic breathing in combination with Kegel exercises is significant in improving pelvic floor muscle function and quality of life among multigravida women with stress urinary incontinence.

The researcher will compare diaphragmatic breathing to kegel exercises as a standard treatment to see if it produces better results for treating SUI Participants will Perform diaphragmatic breathing with kegel exercises for 6 weeks Visit clinic every at the end of every week They will keep a diary regarding when they performed exercises

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • • The population under study was adult women of age between 25-45 years
  • Women with the history of at least two parities
  • No previous history of undergoing any physical therapy treatment for SUI
  • The study included clinically diagnosed women with stress urinary incontinence
  • Study included grade 1-2 severity of SUI that can be treated conservatively
  • Women with both vaginal and c-section deliveries were included

Exclusion criteria

  • Women with pelvic organ prolapse
  • Women that were menopausal or post-menopausal
  • Pregnant women and 6 months post-partum
  • Any other surgical and medical history (congenital urological disease or tumor of bladder)
  • Women with detrusor hyperreflexia
  • Any on-going Infection (vaginal lesion or UTI)
  • Women that had chronic pelvic pain
  • Women that had any sextual disorders
  • Women having any neurological problems

Treatment and study plan

Diaphragmatic breathing

Other

Patient lies supine with pillow under the head and knees. One hand on abdomen and other on chest Patient inhales deeply through the nose till the chest remains still and hand on the abdomen rises

Other names: Deep breathing

Kegel exercises

Other

Patient lies supine with pillow under the head and knees Patient contracts the pelvic floor muscle like holding urine and sustain it for 10-15 seconds

Other names: Pelvic floor exercises

Primary outcomes

  1. Pressure

    Time frame: Baseline (pre-intervention) and 6 weeks (post-intervention)

    a biofeedback device with vaginal probes was used to Measure pelvic floor muscle strength The probe connected to the biofeedback was inserted into the vagina and 55mm of Hg pressure was maintained by inflating the probe through the biofeedback. Strength was assessed by recording the maximum pressure exerted during the voluntary pelvic floor muscle contraction on command. Pressure was recorded in mm of Hg by the device. According to a research manometry results measured in cm H2O unit was categorized according to the modified oxford scale into 0-5 grading scales. 0 indication none and 5 indicating strong contraction to categorize the collected data.

  2. Endurance

    Time frame: Baseline (pre-intervention) and 4 weeks (post-intervention)

    A biofeedback device with vaginal probe was used to measure the endurance of pelvic floor muscles.

    The probe connected to the biofeedback was inserted into the vagina and 55mm of Hg pressure was maintained by inflating the probe through the biofeedback. Endurance was measured by recording the number of seconds a contraction was sustained over a period of 10 seconds. Pressure was recorded in number of seconds, 0 indication none and 10 indicating excellent endurance to categorize the collected data.

  3. Incontinence Quality of Life

    Time frame: Baseline (pre-intervention) and 6 weeks (post-intervention)

    Quality of life of patients suffering from Urinary Incontinence was measured using a questionnaire. The I-QOL questionnaire is based on 6 points scale ranging from 0 = none to 5= very great deal including 22 items. The questionnaire evaluates social life impacts, social embarrassment, psychological impacts and avoiding and limiting behavior associated with urinary incontinence. Total score was calculated using the formula: total score= (obtained sum by total items/110) x 100%. A low score indicated poor quality of life whereas a higher score indicated good quality of life among the patients of SUI. This questionnaire is used worldwide and is highly reliable and valid.

Sponsors and collaborators

Lead sponsor

Lahore University of Biological and Applied Sciences

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 17, 2026
Registry last updated
Apr 17, 2026

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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