To Use the Combined Version of ICIQ-SF and Quality of Life Scale in Mixed Urinary Incontinence
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 100
- Primary Endpoint
- International Consultation on Incontinence Questionnaire Short Form
Study Overview
Brief Summary
The goal of this observational study is detecting the dominant component of mixed urinary incontinence via a combined version of ICIQ-SF and quality of life scale. The main question it aims to answer is:
- Which component (urgency or stress) urinary incontinence bothers the patient more?
Detailed Description
Female patients with mixed urinary incontinence will be given a combined version of ICIQ-SF and quality of life scale on the first visit. Additionally, a bladder diary and 1-hour pad test will be performed on the same visit. After deciding the appropriate treatment, on the 1-month visit (second visit) the same tests will be repeated and scores will be compared.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 90 Years (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Female patients above 18 years old with mixed urinary incontinence
Exclusion Criteria
- •Non-Turkish speakers
- •Poor conscious level
- •Immobile patients
Outcomes
Primary Outcomes
International Consultation on Incontinence Questionnaire Short Form
Time Frame: 1 month
Questionnaire
Bladder diary
Time Frame: 1 month
Diagnostic Test
Pad test
Time Frame: 1 month
Diagnostic Test
Secondary Outcomes
No secondary outcomes reported
Investigators
Ersin Köseoglu
MD
Koç University