The effect of biofeedback on the symptoms of the women with prolapse
Not Applicable
- Conditions
- Pelvic Organ Prolapse.
- Registration Number
- IRCT20180828040898N2
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 20
Inclusion Criteria
Women with pelvic organ prolapse
Women aged 20 to 70 years
Exclusion Criteria
Breastfeeding
previous prolapse surgery
neurological and psychologichal disorders
untreated urinary tract infection
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ?Quality of life. Timepoint: At the beginning of the study and 4 weeks later at the last treatment session. Method of measurement: Prolapse Quality of Life Questionnaire.;Stage of pelvic organ prolapse. Timepoint: At the beginning of the study and 4 weeks later at the last treatment session. Method of measurement: Pelvic Organ Prolapse Quantification system.
- Secondary Outcome Measures
Name Time Method Symptoms of urinary incontinence. Timepoint: At the beginning of the study and after 4 weeks. Method of measurement: International Consultation on Incontinence Questionnaire-Female Lower Urinary Tract Symptoms questionnaire.;Pelvic floor muscle strength. Timepoint: At the beginning of the study and after 4 weeks. Method of measurement: Perineometer instrument.