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Clinical Trial Summary

This project looks to improve the return rate of HPV self-sampling (HPVss) as well as the management of women HPVss positive.


Clinical Trial Description

France has already implemented a cervical screening programme based on HPV test for the whole female population aged 30-65 years. Non-participant women can perform HPV test at their home. However, less than 20% of French women performed vaginal self-sampling when a kit was sent to their home. Women with lower income and educational levels participate less to cervical screening. A variety of personal, practitioner, test-related and logistical barriers negatively impact the screening participation of French women. Key barriers to participation could be addressed by overcoming disparities in HPV-related knowledge and perceptions about cervical cancer screening. This study aims to evaluate the impact of sending HPV self-sampling kit at women's home, associated with providing, through multiple mobile channels, a multi-language decision aid designed for women with lower education accessible via artificial intelligence-based ChatBot. This decision aid will help women review high quality evidence on cervical cancer disease and screening modalities. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05286034
Study type Interventional
Source International Agency for Research on Cancer
Contact Farida Selmouni, Dr
Phone + 33 4 72 73 84 99
Email selmounif@iarc.fr
Status Not yet recruiting
Phase N/A
Start date June 1, 2024
Completion date December 31, 2025

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