HPV Ends Here: Increasing Uptake of the HPV Vaccine
Part of paid clinical trials in Sacramento, California.
- Sponsor
- University of California, Davis
- Study ID
- NCT06831929
- Status
- Recruiting
Conditions
- HPV Vaccine
Eligibility Criteria
- Sex
- ALL
- Age
- 10 Years - 12 Years
- Healthy Volunteers
- Accepted
Interventions
- Intervention Arm — BEHAVIORALWithin the intervention clinics, parents of patients between the ages of 10-12 (who are eligible for the HPV vaccine) will receive a culturally tailored customized HPV vaccine message and testimonial video from a patient/survivor of an HPV associated cancer (e.g., oropharyngeal, or cervical) via the MyChart patient portal. Parents will also receive a personal call from the research coordinator to remind them that their child is due for the HPV vaccine. If the parent is interested in scheduling the HPV vaccine appointment during this call, the research coordinator will transfer the parent to UC Davis appointment call center to schedule the appointment. Also, primary care team members will receive a semi-annual learn at lunch workshop focused on strategies to introduce the HPV vaccine to parents and how to address concerns from vaccine hesitant parents. Workshop content will be tailored/adapted to include patient/parent cultural considerations.
Study Details
Develop, implement, and evaluate a culturally tailored multilevel intervention to increase uptake of the HPV vaccine among eligible patients ages 10-12 of the University of California, Davis Health Community Physician (UCDH CP) primary care practices using a randomized controlled trial design.
Key Dates
- Start date
- Feb 28, 2025
- Status verified
- Apr 2025
- Primary completion
- Jan 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 2,232 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- PREVENTION
Arms
- No Intervention: Control ArmThese clinics will not receive any intervention and will continue with care as usual.
- Experimental: Intervention ArmThese clinics will receive the multilevel intervention which will include tailored parent/patient education, appointment scheduling assistance, and primary care team trainings.
Primary Outcome Measure
Primary Outcome: Evaluation [ Time Frame: One year ]
Central Contacts
- Ramneek Kahlon, BS9167312578
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California Davis Health | Sacramento | California | 95817 | Julie HT Dang, PhD |
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