Actively Recruiting
The STOP-HPV Scale Up Study
Led by University of California, Los Angeles · Updated on 2026-02-27
100000
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
Sponsors
U
University of California, Los Angeles
Lead Sponsor
A
American Medical Group Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
Human papillomavirus (HPV) causes 35,900 US cancer cases per year, 4,000 deaths, and $4 billion in can In this study, the investigators will conduct a 3-arm clustered randomized controlled trial (RCT) in an estimated 72 practices from up to 8 health systems to evaluate the effectiveness and cost effectiveness of two potentially scalable implementation strategies (based on prior work) to increase the initiation of HPV vaccine against a usual care (control) arm. The intervention arms are 1) online provider communication training only ("STOP-HPV-Online" and 2) online provider communication training plus a Learning Collaborative, with performance feedback, attended by practice leads ("STOP-HPV-LC). cer-related costs. It is recommended at ages 11-12 years routinely but can be given starting at ages 9-10 years. Despite having an effective vaccine, HPV vaccine initiation/completion rates in the U.S. were only at 76.8%/61.4% respectively in 2023 among 13-17 year olds; these rates are lower than the other recommended adolescent vaccines. Two key barriers are 1) suboptimal clinician communication to address parental concerns and 2) ineffective office systems causing missed vaccine opportunities.
CONDITIONS
Official Title
The STOP-HPV Scale Up Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient of participating practice
- Well child care visit during the 12-month intervention period
- No prior dose of HPV vaccine at the time of the well child care visit
- Age-eligible (9 to 17 years old)
You will not qualify if you...
- Prior dose of HPV vaccine
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
AMGA
Alexandria, Virginia, United States, 22314
Actively Recruiting
Research Team
P
Peter Szilagyi, MD, MPH
CONTACT
C
Christina Albertin, PhD, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
3
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