Self-sampling by Evalyn BrushSelf sampling by Evalyn Brush home or in GP´s clinic
Self-sampling by Evalyn Brush: Women will perform a cervicovaginal self-sampling at their home using Evalyn Brush.
Self sampling by Evalyn Brush home or in GP´s clinic: Women will perform a cervicovaginal self-sampling at their home or the GP´s clinic using Evalyn Brush
Study summary
The trial will evaluate whether self-sampling and human papillomavirus (HPV) testing may increase cervical cancer screening attendance among under-screened women in Czech Republic. Different ways of offering self-sampling device will be evaluated.
Eligibility
Sex
FEMALE
Min age
30 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria:
* Women with age 30-65 years; for arm A women \> 65 years are allowed
* Women live in the Czech Republic.
* Women who have not participate in cervical cancer screening program in the Czech Republic for at least 3 years (Arm B and C).
* Women with completed informed consent.
* Women capable of self-sampling of cervicovaginal swab.
Exclusion Criteria:
* Pregnant women.
* Women with no sexual intercourse experience.
* Women after hysterectomy including cervix.
Primary outcome measure(s)
Screening participation — 12 months Comparison of the percentages of women who return a cervicovaginal swab sampled by self-sampling device in different arms of the study. Identification of the best approach to address women who do not participate in standard cervical cancer screening program
Prevalence of high-risk HPV — 12 months Evaluation of the prevalence of high-risk human papillomavirus infection in screening population of Czech women within different arms of the study (attenders/non-attenders).
Trial sites (1)
Facility
City
Region
Status
University Hospital Olomouc
Olomouc
Czechia
Recruiting
More The Institute of Molecular and Translational Medicine, Czech Republic trials in Czechia
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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