Self-Collection for Cervical Cancer Screening and HPV Vaccination for Cancer Prevention Among Women in Emergency Care in Northeast Florida

N/ANot Yet RecruitingNCT06607874

Mayo Clinic100 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Human Papillomavirus-Related Cervical Carcinoma

Interventions

Non-Interventional StudyOTHER

Non-Interventional study

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

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.

Time frame: Baseline

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.

Time frame: One month

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.

Time frame: Baseline

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.

Time frame: Up to 6 weeks

Interviews of women who complete the self-collection

Phone or video-based interviews will be conducted with participants who completed self-collection for feedback on the process.