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Spots Global Cancer Trial Database for Efficacy of Offering a Self-sampling Device by the GP to Reach Underscreened Women

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Trial Identification

Brief Title: Efficacy of Offering a Self-sampling Device by the GP to Reach Underscreened Women

Official Title: Efficacy of Offering a Self-sampling Device by the General Practitioner to Reach Women Underscreened in the Routine Cervical Cancer Screening Program Compared to Sending Reminder Letters by the Screening Organization

Study ID: NCT05656976

Conditions

Cervical Cancer

Study Description

Brief Summary: The ESSAG trial invests the impact of offering a free self-sampling device (SSD) on the cervical cancer screening rate of underscreened women. This study is aimed at women between the age of 31 and 65 who did not have a smear taken during the last 6 years. In order to assess the effect of a) providing the SSD, and b) the intervention of the general practitioner (GP) (either face-to-face, either by sending the SSD by letter), a randomized control trial is set up with three arms. The ESSAG trial evolves from a collaboration between Universiteit Gent and Vrije Universiteit Brussel, Katholieke Universiteit Leuven, Universiteit Antwerpen, Sciensano, het Centrum voor Kankeropsporing en het Belgisch Kankerregister, and is funded by "Kom Op Tegen Kanker".

Detailed Description:

Eligibility

Minimum Age: 31 Years

Eligible Ages: ADULT

Sex: FEMALE

Healthy Volunteers: Yes

Locations

Ghent University, Ghent, , Belgium

Contact Details

Name: Kaatje Van Roy

Affiliation: University Ghent

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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