Type of Study:

Interventional

Study Design:

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Screening

Outcome Measure:

Comparison of women's attitude according to the arm: participation or not to a whole screening action

Outcome Description:

Comparison of attitudes among women not attending organized cervical cancer according to the type of intervention or the lack of intervention: participation or not to a whole screening action. Are considered as whole screening action: cervical smear HPV DNA testing on self-collected vaginal sample negative (no infection by a high-risk HPV) HPV DNA testing on self-collected vaginal sample positive (infection by a high-risk HPV) followed by a cervical smear

Outcome Time Frame:

9 months after the beginning of the study (sending of mails)

Safety Issue:

No

Principal Investigator

Ken HAGUENOER

Investigator Role:

Study Director

Investigator Affiliation:

François Rabelais University, Public Health Laboratory, Tours, France

Authority:

France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)

Study ID:

INCA08-KH / APACHE-2

NCT ID:

NCT01588301

Start Date:

February 2012

Completion Date:

December 2012

Related Keywords:

• Cervical Cancer
• Human Papillomavirus Infection
• Cervical Cancer Screening
• Human Papillomavirus (HPV)
• Self-collected vaginal sample
• Cervical Smear
• Uterine Cervical Neoplasms
• Warts
• Papillomavirus Infections