Validation of Korean Version of ICIQ-SF

Urinary Incontinence Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02145806
• Other study ID #: CMC_UI_2014
• Status: Completed
• Phase: N/A
• First received: May 21, 2014
• Last updated: February 12, 2015
• Start date: June 2014
• Est. completion date: September 2014

Study information

• Verified date: February 2015
• Source: The Catholic University of Korea
• Contact: n/a
• Is FDA regulated: No
• Health authority: South Korea: Institutional Review Board
• Study type: Observational [Patient Registry]

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 134
• Est. completion date: September 2014
• Est. primary completion date: September 2014
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

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

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Urinary Incontinence

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
The Catholic University of Korea	National Cancer Center, Korea

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Urinary incontinence		1-2 weeks	No