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Completed

NCT Number: NCT06896500

Investigation Of The Effects Of Kegel Exercises On Vaginal Flatus Among Postpartum Women

Title: Investigation of the Effects of Kegel Exercises on Vaginal Flatus Among Postpartum Women

Brief Summary:

This study aims to evaluate the effectiveness of Kegel exercises in reducing vaginal flatus among postpartum women. Vaginal flatus, the involuntary passage of air through the vagina, is a common but often underreported pelvic floor dysfunction that can affect women's quality of life.

A total of 40 postpartum women were randomly assigned to an experimental group (performing Kegel exercises) or a control group (no intervention). The experimental group performed Kegel exercises three times daily in different positions for six weeks. Vaginal flatus frequency and bother scores were assessed using a validated questionnaire, and sexual quality of life was evaluated with the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12).

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Key information

Age range

20 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Istanbul Medipol University

Istanbul, 34810, Turkey (Türkiye)

About this study

This study is a randomized controlled trial designed to assess the effectiveness of Kegel exercises in reducing vaginal flatus among postpartum women. Vaginal flatus, the involuntary passage of air through the vagina, is a common but often overlooked pelvic floor dysfunction that can negatively impact women's quality of life.

A total of 40 postpartum women were recruited and randomly assigned to either the experimental group, which performed Kegel exercises, or the control group, which received no intervention. Participants in the experimental group were instructed to perform Kegel exercises three times daily in different positions (supine, sitting, and standing) over six weeks. The intervention focused on strengthening the pelvic floor muscles through a combination of fast and slow contractions targeting both Type I and Type II muscle fibers.

The primary outcome measures included vaginal flatus frequency and bother scores, which were assessed using a validated questionnaire before and after the intervention. Additionally, sexual quality of life was evaluated using the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • being between the ages of 20-50,
  • being postpartum at least 6 weeks after the last birth,
  • having a complaint of vaginal flatus, and being willing to exercise

Exclusion criteria

  • being over four months postpartum,
  • current pregnancy,
  • presence of pelvic infection,
  • inability to indicate whether there is vaginal flatus,
  • the presence of gynecological cancer.

Treatment and study plan

Kegel Exercises

Behavioral

Kegel exercises performed three times daily in different positions (supine, sitting, and standing) for three weeks, followed by a six-week home program

Primary outcomes

  1. Vaginal Flatus Frequency Reduction

    Time frame: Baseline to at least 6 weeks postpartum

    The primary outcome is the change in vaginal flatus frequency, assessed via patient-reported questionnaire before and after the intervention. Smaller values indicate less flatus, while higher values signify an increase in flatus.

Sponsors and collaborators

Lead sponsor

merve yilmaz menek

Other

Collaborators

  • Istanbul Medipol University Hospital

Registry information

Acronym: KEGEL-VF

Important dates

Study start
2022
Primary completion
2023
Study completion
2024
First posted
Mar 26, 2025
Registry last updated
Mar 26, 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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