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NCT Number: NCT07576283

Comparative Effects of Hypopressive and Transverses Abdominis Focused Core Training in Postpartum

The study aims to compare the effectiveness of these two core training approaches in improving urinary incontinence, pelvic floor function, and quality of life in postpartum women.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

About this study

The primary outcomes of this study are urinary incontinence, pelvic floor function, and quality of life in postpartum women. These outcomes will be assessed using validated instruments: the International Consultation on Incontinence Questionnaire-Urinary Incontinence (ICIQ-UI) for evaluating the severity of urinary incontinence, the King's Health Questionnaire (KHQ) for assessing the impact on pelvic floor function and health-related quality of life, and the Incontinence Impact Questionnaire (IIQ-7) for measuring the broader impact of incontinence on daily activities and emotional well-being. Outcome measures will be measured at baseline and after 4 weeks. Data analysis will be done by SPSS version 25.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Multiparous women with urinary incontinence
  • Who had undergone normal vaginal delivery
  • Free from any medical and gynecological risk factors and /or conditions
  • Stress urinary incontinence test is positive: Pad test

Exclusion criteria

  • Had neurological impairments or connective tissue disorders
  • Active urinary or vaginal infection in the past 3 months
  • Had known detrusor instability
  • Had undergone previous surgery to alleviate SUI
  • Had pelvic organ prolapse

Treatment and study plan

hypopressive training

Other

Frequency: 3 sessions/week under supervision Duration: 30-40 minutes/session For 6 weeks

transverses abdominis focused core training

Other

3 sessions/week under supervision Duration: 30-40 minutes/session For 6 weeks

Primary outcomes

  1. International Consultation on Incontinence Questionnaire - Urinary Incontinence

    Time frame: 6th week

    The tool is used for assessing urinary incontinence symptoms by measuring the frequency, severity, and impact of urinary leakage on quality of life. It includes specific questions related to how often leakage occurs, the amount of urine lost, and how these symptoms affect various aspects of daily life, providing a comprehensive evaluation of the individual's condition

  2. King's Health Questionnaire

    Time frame: 6th week

    The tool is used for evaluating the impact of urinary incontinence on the quality of life in women, offering a comprehensive understanding of how stress urinary incontinence (SUI) affects their physical, emotional, and social well-being. It is particularly relevant for postpartum women, as it captures the functional limitations and lifestyle disruptions caused by incontinence, making it a valuable instrument for assessing the broader effects of SUI on daily life.

  3. Incontinence Impact Questionnaire

    Time frame: 6th week

    The Incontinence Impact Questionnaire (IIQ) is a validated self-report tool designed to measure the impact of urinary incontinence on a woman's quality of life across physical, social, and emotional domains.30 items divided into four domains:

    Physical activity (6 items), Travel (6 items), Social relationships (10 items), Emotional health (8 items)

Study contacts

Contact information is provided by the study sponsor or research team.

imran amjad

CONTACT

[email protected]

03324390125

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Comparative Effects of Hypopressive and Transverses Abdominis Focused Core Training on Urinary Incontinence, Pelvic Floor Function and Quality of Life in Postpartum

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 8, 2026
Registry last updated
Jun 9, 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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