Reliability of KHQ and ICIQ-SF in Assessing Urinary Incontinence Effects in Polish Women

NCT ID: NCT04619238

Last Updated: 2020-11-06

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

155 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-06-01

Study Completion Date

2019-01-10

Brief Summary

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The aim of this study was to assess the psychometric properties of KHQ and ICIQ-SF in polish women.

Detailed Description

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Purpose The King's Health Questionnaire (KHQ) and the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form are widely used in clinical practice. The aim of this study was to assess the psychometric properties of KHQ and ICIQ-SF in polish women.

Methods One hundred fifty-five women with urinary incontinence (UI) aged between 19-82 years underwent urodynamic investigation and completed both KHQ and ICIQ-SF. To evaluate the factor structure and construct the validity of the KHQ and ICIQ, Principal Component Analysis (PCA) using VARIMAX rotation was conducted for all questionnaire items. PCA results were also confirmed by Spearman's correlations between KHQ and ICIQ items. Moreover, the internal consistency of the KHQ and ICIQ was estimated by way of Cronbach's alpha coefficient (α). Statistical analysis was performed using STATISTICA version 13.1 software (StatSoft, Poland), as well as open source R software (version 3.4.4).

Conditions

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Urinary Incontinence Overactive Bladder Stress Urinary Incontinence Urge Incontinence

Keywords

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king's health questionnaire the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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no urinary incontinence

patients without UI

King's Health Questionnaire

Intervention Type DIAGNOSTIC_TEST

patients fulfilled questionnaire

the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form

Intervention Type DIAGNOSTIC_TEST

patients fulfilled ICIQ-SF questionnaire

stress urinary incontinence

patients with SUI

King's Health Questionnaire

Intervention Type DIAGNOSTIC_TEST

patients fulfilled questionnaire

the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form

Intervention Type DIAGNOSTIC_TEST

patients fulfilled ICIQ-SF questionnaire

overactive bladder

patients with OAB

King's Health Questionnaire

Intervention Type DIAGNOSTIC_TEST

patients fulfilled questionnaire

the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form

Intervention Type DIAGNOSTIC_TEST

patients fulfilled ICIQ-SF questionnaire

mix urinary incontinence

patients with MUI

King's Health Questionnaire

Intervention Type DIAGNOSTIC_TEST

patients fulfilled questionnaire

the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form

Intervention Type DIAGNOSTIC_TEST

patients fulfilled ICIQ-SF questionnaire

Urge

patients with urge incontinence

King's Health Questionnaire

Intervention Type DIAGNOSTIC_TEST

patients fulfilled questionnaire

the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form

Intervention Type DIAGNOSTIC_TEST

patients fulfilled ICIQ-SF questionnaire

Interventions

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King's Health Questionnaire

patients fulfilled questionnaire

Intervention Type DIAGNOSTIC_TEST

the International Consultation on Incontinence Modular Questionnaire (ICIQ-SF) Short Form

patients fulfilled ICIQ-SF questionnaire

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* informed consent
* patients with symptoms of urinary incontinence
* age 18-82 years

Exclusion Criteria

* lack of consent
* inability to understand the study protocol
Minimum Eligible Age

18 Years

Maximum Eligible Age

82 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Medical University of Lublin

OTHER

Sponsor Role lead

Responsible Party

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Katarzyna Skorupska

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tomasz Rechberger, Professor

Role: STUDY_DIRECTOR

Medical University of Lublin

Locations

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Katarzyna Skorupska

Lublin, , Poland

Site Status

Countries

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Poland

Other Identifiers

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2\2020

Identifier Type: -

Identifier Source: org_study_id