NCT07156266

Brief Summary

A randomized clinical trial will be carried out to compare the effectiveness of Kegel and squat exercises in reducing urinary incontinence. The study will include 30 participants diagnosed with urinary incontinence, who will be randomly assigned to either a Kegel exercise group or a squat exercise group. Both groups will perform their respective exercises for 10 minutes, three times daily, over a period of 12 weeks. Outcomes will be assessed using the International Consultation on Incontinence Questionnaire - Female Lower Urinary Tract Symptoms Long Form (ICIQ-FLUTS LF) and the Incontinence Quality of Life (I-QOL) questionnaire

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 8, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 8, 2025

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 10, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

August 27, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 5, 2025

Completed
Last Updated

September 5, 2025

Status Verified

August 1, 2025

Enrollment Period

3 months

First QC Date

August 27, 2025

Last Update Submit

August 27, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Urinary incontinence

    The International Consultation on Incontinence Questionnaire - Female Lower Urinary Tract Symptoms Long Form (ICIQ-FLUTS-LF) will be used to assess the severity of urinary incontinence.

    12 weeks

Secondary Outcomes (1)

  • The Incontinence Quality of Life

    12 Weeks

Study Arms (2)

Group A (Kegal Exercise Group)

EXPERIMENTAL
Procedure: Kegal Exercise

Group B (Squats Exercise Group)

ACTIVE COMPARATOR
Procedure: Squats Exercise

Interventions

Dead Bugs:Participants will begin by lying on their backs with their arms extended overhead and legs bent at a 90-degree angle. While engaging their core muscles, they will gradually lower their arms and legs toward the floor, then return to the starting position. Bridging Exercise: Lying on their backs with knees bent and feet flat on the ground, participants will gently raise their hips upward while activating the pelvic floor muscles, then slowly lower them back to the starting position.

Group A (Kegal Exercise Group)

Sumo Squats: Participants will stand with their feet placed wider than shoulder-width apart and toes pointing outward. They will then squat down, keeping their backs straight and their weight on their heels, pause briefly at the bottom, and return to a standing position. Narrow Squats: With their feet set shoulder-width apart and toes pointing forward or slightly outward, participants will lower their bodies into a squat position while keeping their backs straight and their weight centered in the heels. After a brief pause, they will return to a standing position.

Group B (Squats Exercise Group)

Eligibility Criteria

Age30 Years - 60 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Women who are physically able to perform the required exercises and are willing to provide informed consent to participate in the study.

You may not qualify if:

  • Pregnant women or those planning to become pregnant during the study period. Individuals who have undergone surgery within the past six months that may affect pelvic floor strength or urinary incontinence symptoms.
  • Women with neurological disorders, current urinary tract infections (UTIs), or a history of recurrent UTIs that could influence pelvic floor function or UI symptoms.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Faisalabad

Faisalābad, Punjab Province, 38000, Pakistan

Location

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 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
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

August 27, 2025

First Posted

September 5, 2025

Study Start

February 8, 2025

Primary Completion

May 8, 2025

Study Completion

May 10, 2025

Last Updated

September 5, 2025

Record last verified: 2025-08

Locations