Human Papilloma Virus (HPV) is a cause of cervical cancer in women. This study is being done to identify sites for cervical cancer screening and education regarding HPV vaccination outside of the traditional settings of primary care and gynecologic clinics. Identifying non-traditional cancer screening settings may increase cancer screening completion and HPV vaccination among women with limited health care knowledge and access who are vulnerable to health disparities.
Adults assigned as female at birth age 18-65 with a Mayo Clinic medical record number
Adults assigned as female at birth age 0-17
Adults assigned as female at birth age > 65
Adults assigned as male at birth
Adults assigned as female at birth without a Mayo Clinic medical record number
Female patients recruited after previous ED visits
Cohort
Prospective
Non-Interventional Study
Other interventionNon-Interventional study
Human Papilloma Virus (HPV) sample self-collection following Emergency Department (ED) presentation
Will be assessed by the percentage of women between 25-65 eligible for cervical cancer screening who participate or who opt not to participate in self-collection.
HPV vaccination following ED presentation
Will be assessed by the percentage of women between 18-26 eligible for HPV vaccination for cervical cancer prevention who participate in HPV vaccination. Participants will be contacted one month after initial contact to determine if the HPV vaccination was administered.
Interviews of women who decline self-collection
Phone or video-based interviews will be conducted with eligible participants who decline self-collection to determine reasons for non-participation.
Interviews of women who consent to self-collection but do not complete the self-collection
Phone or video-based interviews will be conducted with participants who agree to participate but do not complete self-collection after 4 weeks to determine reasons for non-participation.
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This trial is not recruiting at the moment. You can still explore other options:
