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Kegel exercise and stress urinary incontinence

Phase 3
Conditions
Stress urinary incontinence.
Stress Urinary Incontinence
Registration Number
IRCT20180527039868N1
Lead Sponsor
Sultan Qaboos University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
70
Inclusion Criteria

Non-pregnant females.
Able to read and write
Attending the primary healthcare centers for any reason

Exclusion Criteria

Females in the postnatal period (who delivered in the past 6 months).
Women requiring wheel-chair.
Women attending for emergency services.
Women with prolapse grade III and IV according to the classification of International Continence Society (ICS)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The frequency of Stress Urinary Incontinence symptoms. Timepoint: At baseline and 12 weeks after intervention. Method of measurement: International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-SF).;The severity of Stress Urinary Incontinence symptoms. Timepoint: At baseline and 12 weeks after intervention. Method of measurement: International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-SF).;The quality of life of women with Stress Urinary Incontinence. Timepoint: At baseline and 12 weeks after intervention. Method of measurement: International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-SF).
Secondary Outcome Measures
NameTimeMethod
Measure Pelvic Floor Muscle (PFM) strength. Timepoint: At baseline and 12 weeks after intervention. Method of measurement: Vaginal palpation (Oxford Grading System).;Measure Pelvic Floor Muscle (PFM) strength and endurance. Timepoint: At baseline and 12 weeks after intervention. Method of measurement: Perineometer.
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