Patient Satisfaction Survey of Non-surgical Urinary Incontinence Treatment
NCT ID: NCT04064970
Last Updated: 2020-10-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
125 participants
OBSERVATIONAL
2019-03-14
2020-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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PASS Cohort
patient acceptable symptom state (PASS)
The Severity Index for Urinary Incontinence, which documents incontinence frequency and severity, pelvic floor distress, patient global impression of severity and improvement, physical function, depression, sleep disturbance, anxiety, global health and ability to participate in social roles and activities.
Interventions
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patient acceptable symptom state (PASS)
The Severity Index for Urinary Incontinence, which documents incontinence frequency and severity, pelvic floor distress, patient global impression of severity and improvement, physical function, depression, sleep disturbance, anxiety, global health and ability to participate in social roles and activities.
Eligibility Criteria
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Inclusion Criteria
* English-speaking
* Possess the ability to complete electronic patient reported outcome questionnaires and voiding diaries
Exclusion Criteria
* Women were unable to complete electronic patient reported outcome questionnaires
* Women with greater than stage II uterovaginal prolapse or post-hysterectomy prolapse.
* Women considered citizens of the European Union (EU), including EU citizens living in the United States.
18 Years
FEMALE
No
Sponsors
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University of Rochester
OTHER
Responsible Party
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Erin Duecy
Professor
Locations
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University Urogynecology Associates
Rochester, New York, United States
Countries
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Other Identifiers
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RSRB72759
Identifier Type: -
Identifier Source: org_study_id
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