Validation of Korean Version of ICIQ-SF

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02145806

Enrollment

134

Registered

2014-05-23

Start date

2014-06-30

Completion date

2014-09-30

Last updated

2015-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary Incontinence

Keywords

Urinary incontinence, Validation study, Pregnant women, Postpartum period

Brief 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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Urinary incontinence	1-2 weeks

Outcome results