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To Use the Combined Version of ICIQ-SF and Quality of Life Scale in Mixed Urinary Incontinence

To Use the Combined Version of ICIQ-SF and Quality of Life Scale in Mixed Urinary Incontinence

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05948397
Enrollment
100
Registered
2023-07-17
Start date
2023-08-01
Completion date
2025-08-01
Last updated
2023-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Incontinence, Urge, Incontinence Stress, Quality of Life

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: 1\. 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.

Interventions

DIAGNOSTIC_TESTCombined version of International Consultation on Incontinence Questionnaire Short Form (ICIQ SF) and quality of life scale

A combined version of International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF) and quality of life scale would be given to all patients. The sum of the responses for the third, fourth and fifth questions and quality of life scale scores will be recorded.

DIAGNOSTIC_TESTBladder diary

Bladder diary is an online application. Frequency, nocturia, functional bladder capacities will be reported. More than 8 urination during daytime will be recorded as overactive bladder. More than 1 interruption of sleep for urination at night is nocturia. Functional bladder capacity below 100 ml will be defined as decreased bladder capacity, while capacity over 400 ml will be reported as increased bladder capacity and compliance

DIAGNOSTIC_TESTPad test

One-hour pad test. * the test is started by putting one pre-weighted pad without patient voiding, -patient drinks 500 ml of sodium-free liquid in \<15 min- then sits or rests, * patient walks for 30 min, including climbing one flight of stairs (up and down), * patient performs the following activities: standing up from sitting (10 ), coughing vigorously (10 ), running on the spot for 1 min, bending to pick up an object from the floor (5 ), and washing hands in running water for 1 min (this activity program may be modified according to the patient's physical fitness), * the total amount of urine leaked is determined by weighing the pad. In the analysis of 1-hr pad test, an increase of 1-10 g is classified as representing mild incontinence, 11-50 g moderate and \>50 g severe incontinence. The values for 24-hr pad test are classified as follows: Mild (4-20 g/ 24 hr), moderate (21-74 g/24 hr), and severe (\>75 g/24 hr) incontinence

Sponsors

Koç University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 90 Years
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

Design outcomes

Primary

MeasureTime frameDescription
International Consultation on Incontinence Questionnaire Short Form1 monthQuestionnaire
Pad test1 monthDiagnostic Test
Bladder diary1 monthDiagnostic Test

Contacts

Primary ContactTufan Tarcan, Prof
bilgi@tufantarcan.com905434948365
Backup ContactErsin Köseoğlu
ersinkoseoglu@ku.edu.tr905306930442

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026