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 — BEHAVIORAL
    Within 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 Arm
    These clinics will not receive any intervention and will continue with care as usual.
  • Experimental: Intervention Arm
    These 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

Locations (1)

FacilityCityStateZIPSite coordinators
University of California Davis HealthSacramentoCalifornia95817
Julie HT Dang, PhD

Find similar trials in Sacramento, CA