We propose a cross-sectional study to explore the acceptability and feasibility of HPV self-sampling among Quebec women. The study will invite eligible women to self-sample for HPV at home. The HPV risk factors of patients included in the study will be taken into consideration (vaccination, smoking, number of partners, date of last screening, etc.).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SCREENING
Masking
NONE
Enrollment
400
HPV self-sampling (Cobas Uniswab)
Centre Hospitalier Universitaire de Sherbrooke
Sherbrooke, Quebec, Canada
Evaluate the acceptability of HPV self-sampling by patients
percentage of patients who prefer HPV testing to traditional cytology
Time frame: 2 months following recruitment
Evaluate the percentage of samples collected correctly by patients
Time frame: 2 months following recruitment
Evaluate the return rate of mailed kits
Time frame: 2 months following recruitment
Calculate the HPV positivity rate in a population sample
Time frame: 2 months following recruitment
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