Breast Cancer-Related Approach for Increasing Cervical Cancer Screening
Recruiting
N/A
Interventional Study
Cervical Cancer Screening
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
- 50 – 74
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 4,500 (estimated)
- Sponsor
- Jessica Di Vincenzo Sormani · Other
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About This Trial
The primary objective of this clinical trial is to assess cervical cancer screening participation among under-screened women invited through organized breast cancer screening programs in Switzerland.
This randomized trial will compare three arms:
1. Intervention group 1: Sensitization to Cervical Cancer (CC) screening Women will receive an awareness letter explaining the importance of cervical c…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Women receiving Breast Cancer Screening (BCS) invitation letters in the selected five cantons (Geneva, Bern (francophone), Jura, Neuchâtel, and Vaud)
* Aged 50 to 74 years old
* Not been screened for cervical cancer in the past three years
* Speaking one of the 6 languages of …
Contacts
Patrick Petignat, MD
CONTACT