About this trial
This project will compare the uptake of cervical cancer screening through ED HPV sampling among patients presenting to the ED.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Cisgender women and transgender/non-binary individuals with a cervix,
Age 30 - 65 years, and demonstrating decisional capacity to consent to participate with no known
Disqualifiers
Past hysterectomy with cervical removal
Known infection with HIV (as screening recommendations for people with HIV differ from the general population)
Inability to consent (e.g., lacking decisional capacity, intoxicated, or in distress)
Current pregnancy or in the three months after giving birth
Trial design
Single group
Treatments tested in this trial
Cervical Cancer Screening
Diagnostic testSubjects will perform self sampling for cervical cancer.
Treatment groups
Trial outcomes
Primary outcomes
Uptake of cervical cancer screening from self-sampling in the ED
Number of subjects referred for additional screening who follow through with next steps in the screening process.
Sponsors and contacts
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