HPV Self-Collection Program

Recruiting N/A Interventional Study
HPV
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
25 – 65
Sex
Female
Study type
Interventional
Purpose
Health Services Research
Participants needed
1,000 (estimated)
Sponsor
University of Utah · Other
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About This Trial
The objective of the study is to develop, pilot, and analyze the effectiveness of HPV self-collection programs which will be used to follow up among women overdue for cervical cancer screening. The investigators will develop protocols for in-clinic and home-based HPV-self-collection programs and follow-up system for HPV-positive tests for community health centers and/or clinics. The program is mea…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Women and individuals with a cervix. * Aged 25-65 years during the study measurement period. * Qualifying visit to the participating clinic. * Overdue for cervical cancer screening. * Those aged 24-64 who have not had cervical cytology (i.e., Pap test) performed within the las…
Contacts

Deanna Kepka

801-587-4565

Deanna.Kepka@hci.utah.edu

CONTACT