Efficacy of Strategies Involving Self-sampling to Reach Women Not Participating in Regular Cervical Cancer Screening (CapU4)
Cancer Screening Test
About this trial
This is an interventional screening trial for Cancer Screening Test focused on measuring cervical cancer, screening coverage, cancer screening test, under-screened women, urinary self-sampling, vaginal self-sampling, randomised controlled trial, semi-structured interviews
Eligibility Criteria
Inclusion Criteria:
- women aged between 30 and 65 years
- living in the Departments of Mayenne and Sarthe (Pays de la Loire, France)
- who have not carried out a screening test (cytology of smear or HPV test) following a letter sent 12 months previously in 2020.
Exclusion Criteria:
- recent cervical sampling (less than three years old)
- women younger than 30 or older than 65 years
- women who have had a hysterectomy
- women with ongoing follow-up for a cervical lesion
- women who are not members or beneficiaries of a social security system.
Sites / Locations
- CRCDC Pays de la LoireRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Experimental
Experimental
control
vaginal self-sampling
urinary self-sampling
The control arm corresponds to women receive a conventional invitation letter sent by post to the home address of eligible women recommending them to make an appointment to a doctor or a midwife for the collection of a cervical specimen.
eligible women receive at their home address a vaginal self-sampling kit in addition to the conventional invitation letter
eligible women receive at their home address a urine collection kit in addition to the conventional invitation letter