Self-Collection for Cervical Cancer Screening and HPV Vaccination for Cancer Prevention Among Women in Emergency Care in Northeast Florida
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Non-Interventional Study.
- Who it may be relevant to
- Registry conditions: Human Papillomavirus-Related Cervical Carcinoma. Basic parameters: 18 years — 65 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Eligibility and Participation Characteristics of a Pilot Study of Self-Collection for Cervical Cancer Screening and HPV Vaccination for Cancer Prevention
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.
Interventions
- Other Non-Interventional Study
Non-Interventional study
Primary outcome measures
- Human Papilloma Virus (HPV) sample self-collection following Emergency Department (ED) presentation [Time frame: Baseline]
- HPV vaccination following ED presentation [Time frame: One month]
- Interviews of women who decline self-collection [Time frame: Baseline]
- Interviews of women who consent to self-collection but do not complete the self-collection [Time frame: Up to 6 weeks]
- Interviews of women who complete the self-collection [Time frame: Up to 6 weeks]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- Mayo Clinic in Florida — Jacksonville
Identifiers
NCT: NCT06607874 · 23-009193 · NCI-2024-07532 · 23-009193