ClinicalTrials.Veeva

Menu

Identification of the UDI-6 and the IIQ-7 Cutoff Scores in Urinary Incontinent Women

M

Medical University of Lublin

Status

Completed

Conditions

Quality of Life
Urinary Incontinence,Stress
Urinary Incontinence

Treatments

Diagnostic Test: UDI-6
Diagnostic Test: IIQ-7
Diagnostic Test: ICIQ-SF

Study type

Observational

Funder types

Other

Identifiers

NCT04433715
01/2020

Details and patient eligibility

About

Purpose Urogenital Distress Inventory-6 (UDI-6), Incontinence Impact Questionnaire-7 (IIQ-7) and The International Consultation on Incontinence (ICIQ-SF) Short Form are used to diagnose individuals with urinary incontinence (UI) and to assess the impact of the dysfunction on patient quality of life. While ICIQ-SF has fixed cutoff values - UDI-6 and IIQ-7 do not. We aimed to find the cutoff scores for UDI-6 and IIQ-7 in women with UI.

Methods The study involved 205 women aged between 31 and 83 years - 155 with, and 50 without UI symptoms. All participants completed all three questionnaires: ICIQ-SF, UDI-6 and IIQ-7. Patients were categorized according to their ICIQ-SF scores, as symptomatic ICIQ-SF ≥6 (n=134) and asymptomatic ICIQ < 6 (n=60). The Receiver Operating Characteristics (ROC) curve was used to test how well UDI-6 allowed a discrimination between patients suffering from UI and those who do not. AUC (Area under Curve) statistic was calculated to measure the UDI-6 and IIQ-7 Total Score efficiency.

Full description

Purpose Urogenital Distress Inventory-6 (UDI-6), Incontinence Impact Questionnaire-7 (IIQ-7) and The International Consultation on Incontinence (ICIQ-SF) Short Form are used to diagnose individuals with urinary incontinence (UI) and to assess the impact of the dysfunction on patient quality of life. While ICIQ-SF has fixed cutoff values - UDI-6 and IIQ-7 do not. We aimed to find the cutoff scores for UDI-6 and IIQ-7 in women with UI.

Methods The study involved 205 women aged between 31 and 83 years - 155 with, and 50 without UI symptoms. All participants completed all three questionnaires: ICIQ-SF, UDI-6 and IIQ-7. Patients were categorized according to their ICIQ-SF scores, as symptomatic ICIQ-SF ≥6 (n=134) and asymptomatic ICIQ < 6 (n=60). The Receiver Operating Characteristics (ROC) curve was used to test how well UDI-6 allowed a discrimination between patients suffering from UI and those who do not. AUC (Area under Curve) statistic was calculated to measure the UDI-6 and IIQ-7 Total Score efficiency.

Enrollment

155 patients

Sex

Female

Ages

31 to 83 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • UI symptoms

Exclusion criteria

  • lack of consent, oncological diseases

Trial design

155 participants in 2 patient groups

patients with UI symptoms
Description:
All participants completed all three questionnaires: ICIQ-SF, UDI-6 and IIQ-7.
Treatment:
Diagnostic Test: IIQ-7
Diagnostic Test: UDI-6
Diagnostic Test: ICIQ-SF
patients without UI symptoms
Description:
All participants completed all three questionnaires: ICIQ-SF, UDI-6 and IIQ-7.
Treatment:
Diagnostic Test: IIQ-7
Diagnostic Test: UDI-6
Diagnostic Test: ICIQ-SF

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems