Validity and Reliability of the PRAFAB

NCT07339657 · tracked via the Priya Life Science Turkey tracker

Sponsor

Afyonkarahisar Health Sciences University

Phase

Observational

Started

2024-10-15

Last updated

2026-01-14

Condition(s) studied

Urinary Incontinence

Investigational drug(s) / intervention(s)

Construct validityTest-retest reliability

Construct validity: This is not an intervention. This is an analysis conducted to examine the factor structure of this questionnaire. The analysis will be performed using the SPSS 26.0 software package program.

Test-retest reliability: This is not an intervention. This is an analysis conducted to examine the repeatability of this questionnaire. The analysis will be performed using the SPSS 26.0 software package program.

Study summary

PRAFAB assesses both the objective and subjective aspects of urinary incontinence. While differing from other questionnaires in this respect, it consists of only five questions. Today, there is a need for multidimensional and easy-to-use scales that can assess the effects of incontinence on quality of life. Therefore, the aim of this study is to conduct a Turkish validity and reliability study of the PRAFAB questionnaire in women with urinary incontinence.

Eligibility

Sex

FEMALE

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Being 18 years of age or older * Have been diagnosed with urinary incontinence by a urologist * Be female Exclusion Criteria: * Being pregnant, * Being in the early postpartum period, * Have been diagnosed with bladder cancer, diabetic nephropathy, a history of central nervous system damage, congenital urological disorders, urinary tract infection, neurogenic bladder, severe cognitive impairment, and severe psychiatric illness.

Primary outcome measure(s)

PRAFAB — This questionnaire, which takes approximately 2-3 minutes to complete, will be administered to participants twice at two-week intervals.
It is a 5-item questionnaire. Developed to assess the severity of urinary incontinence and its impact on the individual.

Trial sites (1)

Facility	City	Region	Status
Emel Taşvuran Horata	Afyonkarahisar	Merkez	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07339657 on ClinicalTrials.gov ↗ ← All trials in Turkey