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Clinical Trials/CTRI/2025/03/082376
CTRI/2025/03/082376Not yet recruitingNot Applicable

A study to assess effectiveness of multifaceted bladder training programme on continence and quality of life among parous women with stress urinary incontinenceat selected rural areas, Mangaluru

Amisha S Amin1 site in 1 country220 target enrollmentStarted: March 30, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
220
Locations
1
Primary Endpoint
improvement in quality of life, strength of perineal muscle and decrease in stress urinary incontinence

Study Overview

Brief Summary

women face various health problems during pregnancy and after delivery. One such problem faced during childbirth, and which continues after delivery for lifetime is stress urinary incontinence. This occurs because of weakened pelvic floor muscles during childbirth. stress urinary incontinence affects quality of life of women. It may affect her in doing day to day activities, social activities, travelling, sexual life with husband and many other. Though many women face this problem, they fail to express it or ignore it as young adults and face serious problems like vaginal infection, genital rashes, urinary leakage, bad odor due to urine leakage etc.

Multifaceted bladder training programme in this study includes Kegels exercise, urge suppression technique and lifestyle modification teaching. These techniques are known to increase perineal strength and gain control over urination. So, this study is aimed to assess effectiveness of multifaceted bladder training programme among parous women with stress urinary incontinence.

Study Design

Study Type
Interventional
Allocation
Stratified randomization
Masking
Not Applicable

Eligibility Criteria

Ages
25.00 Year(s) to 40.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • •Parous women who are aged between 25-40 years with history of at least one vaginal delivery willing to participate in the study know to read and write Kannada or English available at the time of data collection.

Exclusion Criteria

  • •Parous women who are on treatment for incontinence like pharmacological treatment, pelvic floor physiotherapy and surgery for incontinence management chronic co-morbid illness like high-grade uterine prolapse and pelvic cancer History of vaginal delivery in last 12 months Previous participation in PFMT program Pregnant at the time of data collection.

Outcomes

Primary Outcomes

improvement in quality of life, strength of perineal muscle and decrease in stress urinary incontinence

Time Frame: 12 weeks

Secondary Outcomes

  • improving quality of life of women(12 weeks)

Investigators

Sponsor
Amisha S Amin
Sponsor Class
Other [self]

Study Sites (1)

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