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Can an informational flip chart on pelvic floor muscle training and lifestyle advice improve the quality of life for Nepali women with a pelvic organ prolapse? A randomised control trial

Not Applicable
Completed
Conditions
Pelvic organ prolapse
Reproductive Health and Childbirth - Other reproductive health and childbirth disorders
Public Health - Health promotion/education
Registration Number
ACTRN12618000011280
Lead Sponsor
Delena Caagbay
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
140
Inclusion Criteria

Women attending POP screening camps at two urban hospitals in Kathmandu Valley with a symptomatic pelvic organ prolapse stage I-III (as measured using the Pelvic Organ Prolapse Quantification System - POP-Q) are eligible for this study

Exclusion Criteria

Women who are pregnant, breastfeeding, have had gynaecological cancer, mental illness, have a stage IV POP and those who have been previously taught PFMT

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in mean score for the validated Prolapse-Quality of Life (P-QoL) questionnaire[The P-QoL will be administered at 6 weeks, 12 weeks and 6 months after the intervention. The primary endpoint will be at 6 months.]
Secondary Outcome Measures
NameTimeMethod
Frequency of performing PFMT as recorded in a daily diary[6 weeks, 12 weeks and 6 months after intervention]
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