Actively Recruiting

Phase Not Applicable
Age: 9Years - 17Years
All Genders
NCT06831383

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

Age: 9Years - 17Years
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

AMGA

Alexandria, Virginia, United States, 22314

Actively Recruiting

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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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