NCT02145806

Brief Summary

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

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
134

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2014

Shorter than P25 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 21, 2014

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 23, 2014

Completed
9 days until next milestone

Study Start

First participant enrolled

June 1, 2014

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2014

Completed
Last Updated

February 13, 2015

Status Verified

February 1, 2015

Enrollment Period

3 months

First QC Date

May 21, 2014

Last Update Submit

February 12, 2015

Conditions

Urinary Incontinence

Keywords

Urinary incontinenceValidation studyPregnant womenPostpartum period

Outcome Measures

Primary Outcomes (1)

  • Urinary incontinence

    1-2 weeks

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

130

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Urinary Incontinence

Condition Hierarchy (Ancestors)

Urination DisordersUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesLower Urinary Tract SymptomsUrological ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Target Duration
1 Week
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

May 21, 2014

First Posted

May 23, 2014

Study Start

June 1, 2014

Primary Completion

September 1, 2014

Study Completion

September 1, 2014

Last Updated

February 13, 2015

Record last verified: 2015-02