HPV Self-sampling in the General Population
Recruiting
N/A
Interventional Study
Cervical Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 30 – 65
- Sex
- Female
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 6,000 (estimated)
- Sponsor
- International Agency for Research on Cancer · Other
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About This Trial
A randomized controlled trial comparing three strategies for cervical cancer screening: direct mailing of HPV self-sampling kit ("Outreach" arm), choice between self-sampling or healthcare provider sampling ("Choice" arm), and standard care (control arm) in two French departments.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Women aged 30 to 65 years old
* Living in the study area (Departments of Marne and Aube, France)
* At moderate risk of cervical cancer, i.e. eligible to the organised programme and receiving the first invitation of the screening round (not a reminder letter)
Exclusion Criteri…
Contacts