NCT03589352

Brief Summary

The hypothesis of the investigators is that women don't have all the needfull knowledge to understand the importance of a regular gynaecological aftercare. The main objective is to assess women's knowledge's about gynaecological aftercare. The second objective is to identify barriers that prevent women of a regular gynaecological aftercare

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2018

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

Study Start

First participant enrolled

July 1, 2018

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

July 4, 2018

Completed
13 days until next milestone

First Posted

Study publicly available on registry

July 17, 2018

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2019

Completed
Last Updated

July 19, 2018

Status Verified

July 1, 2018

Enrollment Period

1 year

First QC Date

July 4, 2018

Last Update Submit

July 17, 2018

Conditions

Gynecology

Keywords

gynaecological aftercarecontraceptionbreast cancercervix cancercervical screeningbreast self examinationmammographymidwifebody knowledgepreventionself care

Outcome Measures

Primary Outcomes (1)

  • questionnaire

    Assessment of women's knowledge of gynecological follow-up via a questionnaire. The score is calculated from the questionnaire 24 hours before the discharge of patients from the gynecology department

    24 hours before the discharge of patients from the gynecology department

Eligibility Criteria

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

\- women who are able to read and write French

You may qualify if:

  • women aged over eighteen years old
  • women who are able to read and write French

You may not qualify if:

  • women aged under eighteen years old
  • women who aren't able to read or write French

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service de Gynécologie (CMCO)

Strasbourg, 67091, France

RECRUITING

MeSH Terms

Conditions

Breast NeoplasmsUterine Cervical NeoplasmsBreast Self-Examination

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue DiseasesUterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsUterine Cervical DiseasesUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesSelf-ExaminationHealth BehaviorBehavior

Central Study Contacts

Catherine WOLLJUNG-BOUR, Nurse

CONTACT

33 3 69 55 35 78catherine.wolljung-bour@chru-strasbourg.fr

Madeline KETTERLIN, Nurse

CONTACT

33 3 69 55 35 78madeline.ketterlin@etu.unistra.fr

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 4, 2018

First Posted

July 17, 2018

Study Start

July 1, 2018

Primary Completion

July 1, 2019

Study Completion

July 1, 2019

Last Updated

July 19, 2018

Record last verified: 2018-07

Locations

FR(1)