100000 Participants NeededMy employer runs this trial

STOP-HPV Strategies for Human Papillomavirus Vaccines

PS
CA
Overseen ByChristina Albertin, PhD, MPH
Age: < 18
Sex: Any
Trial Phase: Academic
Sponsor: University of California, Los Angeles
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Who Is on the Research Team?

PS

Peter Szilagyi, MD, MPH

Principal Investigator

University of California, Los Angeles

Are You a Good Fit for This Trial?

Inclusion Criteria

Patient of participating practice
My child had a well child check-up in the past 12 months.
I am within the required age range for this study.
See 1 more

Exclusion Criteria

I have received at least one dose of the HPV vaccine.

What Are the Treatments Tested in This Trial?

Interventions

  • STOP-HPV-LC
  • STOP-HPV-Online

How Is the Trial Designed?

3

Treatment groups

Experimental Treatment

Active Control

Group I: STOP-HPV OnlineExperimental Treatment1 Intervention
Group II: STOP-HPV LCExperimental Treatment1 Intervention
Group III: Usual CareActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, Los Angeles

Lead Sponsor

Trials
1,594
Recruited
10,430,000+

American Medical Group Association

Collaborator

Trials
3
Recruited
105,000+

National Cancer Institute (NCI)

Collaborator

Trials
14,080
Recruited
41,180,000+