Ignite Creation Date:
2024-05-06 @ 11:04 AM
Last Modification Date:
2024-10-26 @ 12:39 PM
Study NCT ID:
NCT03420157
Status:
COMPLETED
Last Update Posted:
2019-07-18
First Post:
2018-01-17
Brief Title:
Carrying Out of Focus Group to Improve Cervical Screening Proposal by Vaginal Self-sampling APACHE-4FG
Sponsor:
University Hospital Tours
Organization:
University Hospital Tours
Study Overview
Official Title:
Carrying Out of Focus Group to Improve Cervical Screening Proposal by Vaginal Self-sampling APACHE-4FG
Status:
COMPLETED
Status Verified Date:
2019-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
APACHE-4FG
Brief Summary:
Despite the existence of an effective screening test pap smear cervical cancer is every year in France the cause of more than 3000 new cases and 1100 deaths But in France 4 in 10 women are not screened or not often enough nearly 7 millions women It is therefore necessary to develop new strategies to reach these women The etiological factor of this cancer is persistent infection with oncogenic High-Risk Human PapillomaVirus HR-HPV Thereby HPV-based tests could be alternative screening tests Vaginal self-sampling with HR-HPV test is simpler and less intrusive than the pap smear It has been shown that vaginal self-sampling with HPV test is a powerful means to increase the participation rate in cervical cancer screening The investigators hypothesize that it is possible to optimize participation rate by improving the communication media associated to the vaginal self-sampling kit This is why the accompanying letter and the leaflet explaining how to perform the vaginal self-sampling will be submit to women opinion by using the Focus Group method The objective is to identify improvement ideas of these two communication media
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None