NCT07576283

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress91%
Oct 2025Jun 2026

Study Start

First participant enrolled

October 1, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

May 4, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 8, 2026

Completed
24 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

May 8, 2026

Status Verified

May 1, 2026

Enrollment Period

7 months

First QC Date

May 4, 2026

Last Update Submit

May 4, 2026

Conditions

Keywords

urinary incontinencepelvic floor functionquality of lifepostpartumfemale

Outcome Measures

Primary Outcomes (3)

  • International Consultation on Incontinence Questionnaire - Urinary Incontinence

    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

    6th week

  • King's Health Questionnaire

    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.

    6th week

  • Incontinence Impact Questionnaire

    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)

    6th week

Study Arms (2)

hypopressive training

EXPERIMENTAL

Exercises were conducted in various postures to challenge the body differently and enhance muscular endurance

Other: hypopressive training

transverses abdominis focused core training

ACTIVE COMPARATOR

Teach correct pelvic floor and TrA activation; build foundational strength

Other: transverses abdominis focused core training

Interventions

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

hypopressive training

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

transverses abdominis focused core training

Eligibility Criteria

Age18 Years - 35 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailspostpartum
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Al-madawah rehabilitation clinic

Lahore, Punjab Province, 6400, Pakistan

RECRUITING

Related Publications (5)

  • Molina-Torres G, Moreno-Muñoz M, Rebullido TR, Castellote-Caballero Y, Bergamin M, Gobbo S, et al. The effects of an 8-week hypopressive exercise training program on urinary incontinence and pelvic floor muscle activation: A randomized controlled trial. Neurourology and Urodynamics. 2023;42(2):500-9

    BACKGROUND
  • Katz CMS, Barbosa CP. Effects of hypopressive exercises on pelvic floor and abdominal muscles in adult women: A systematic review of randomized clinical trials. Journal of Bodywork and Movement Therapies. 2024;37:38-45.

    BACKGROUND
  • Abd elglil AA, Mahmoud NSA. Effect of hypopressive exercises versus pelvic floor muscle exercises on stress urinary incontinence among multiparous women. Assiut Scientific Nursing Journal. 2023;11(40):162-74.

    BACKGROUND
  • Soomro KUQ, Mughal SA, Hussain SA, Rajpar ZH, Shaikh AQ, Shaikh A. Pelvic Floor Muscle Exercise plus Core Stability Exercise on Urinary Incontinence in Females. Journal of The Society of Obstetricians and Gynaecologists of Pakistan. 2024;14(2):139-42.

    BACKGROUND
  • Sikora K. The Effects of Core Stability Training on Improving Quality of Life and Symptom Severity in Females with Stress and Mixed Urinary Incontinence: A Meta-Analysis: California State University, Fresno; 2023.

    BACKGROUND

MeSH Terms

Conditions

Urinary Incontinence

Condition Hierarchy (Ancestors)

Urination DisordersUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesLower Urinary Tract SymptomsUrological ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • hina gul, PhD*

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 4, 2026

First Posted

May 8, 2026

Study Start

October 1, 2025

Primary Completion

May 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

May 8, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations