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

Not yet recruiting
Conditions
Human Papillomavirus-Related Cervical Carcinoma
Registration Number
NCT06607874
Lead Sponsor
Mayo Clinic
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
100
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Human Papilloma Virus (HPV) sample self-collection following Emergency Department (ED) presentationBaseline

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 presentationOne 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-collectionBaseline

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-collectionUp 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-collectionUp to 6 weeks

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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mayo Clinic in Florida

🇺🇸

Jacksonville, Florida, United States

Mayo Clinic in Florida
🇺🇸Jacksonville, Florida, United States
Clinical Trials Referral Office
Contact
855-776-0015
mayocliniccancerstudies@mayo.edu
Caroline Chang
Contact
904-953-4637
Chang.Caroline@mayo.edu
Christopher C. DeStephano, MD, MPH
Principal Investigator

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