Human Papillomavirus-Related Cervical Carcinoma
Conditions
Brief summary
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.
Interventions
OTHERNon-Interventional Study
Non-Interventional study
Sponsors
Mayo Clinic
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
* Adults assigned as female at birth age 18-65 with a Mayo Clinic medical record number
Exclusion criteria
* 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Human Papilloma Virus (HPV) sample self-collection following Emergency Department (ED) presentation | Baseline | 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 | One month | 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 | Baseline | 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 | Up to 6 weeks | 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. |
| Interviews of women who complete the self-collection | Up to 6 weeks | Phone or video-based interviews will be conducted with participants who completed self-collection for feedback on the process. |
Countries
United States
Contacts
CONTACTClinical Trials Referral Office
CONTACTCaroline Chang
PRINCIPAL_INVESTIGATORChristopher C. DeStephano, MD, MPH
Mayo Clinic
Outcome results
None listed