Validation of Korean Version of ICIQ-SF

1. Validation of the Korean version of the ICIQ-UI SF for pregnant and postpartum women 2. Evaluation the effect of urinary incontinence in pregnant and postpartum women.

Completed

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Key information

Conditions

Urinary Incontinence Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Lower Urinary Tract Symptoms Male Urogenital Diseases Pathological Conditions, Signs and Symptoms Signs and Symptoms Urination Disorders Urogenital Diseases Urologic Diseases Urological Manifestations

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Being pregnant or postpartum ≤ 3 weeks
Able to read and understand Korean
At least 18 years of age

Exclusion criteria

Refuse to participate in the study
Pelvic inflammatory disease
Psychiatric disease
Needed to be treated in the 7 days

Treatment and study plan

Primary outcomes

Urinary incontinence

Time frame: 1-2 weeks

Sponsors and collaborators

Lead sponsor

The Catholic University of Korea

Other

Collaborators

National Cancer Center, Korea

Registry information

Important dates

Study start: 2014
Primary completion: 2014
Study completion: 2014
First posted: May 23, 2014
Registry last updated: Feb 13, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed