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

Mayo Clinic

Status: Not yet enrolling

Conditions: Human Papillomavirus-Related Cervical Carcinoma

Treatments: Other: Non-Interventional Study

Study type: Observational

Funder types: Other

Identifiers

NCT06607874

23-009193 (Other Identifier)

NCI-2024-07532 (Registry Identifier)

Details and patient eligibility

About

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.

Enrollment: 100 estimated patients

Sex: Female

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

100 participants in 2 patient groups

Observational aim 1 & aim 3

Description:

Patients may choose to undergo HPV vaginal swab self-collection on study in the research clinic or at home. Patients may choose to complete an interview on study. In addition, patients have their medical records reviewed on study.

Treatment:

Other: Non-Interventional Study

Observational aim 2

Description:

Patients are contacted by the study Clinical Research Coordinator (CRC) by phone on study and informed of HPV vaccination eligibility, asked interest in being vaccinated, and informed of sites for HPV vaccination. Patients are then contacted again by the CRC to determine if HPV vaccination occurred.

Treatment:

Other: Non-Interventional Study