RecruitingNot ApplicableNCT06831383

The STOP-HPV Scale Up Study


Sponsor

University of California, Los Angeles

Enrollment

100,000 participants

Start Date

Mar 23, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 9 YearsMax Age: 17 Years

Plain Language Summary

Simplified for easier understanding

This study tests two strategies for improving HPV (human papillomavirus) vaccination rates in primary care practices: an online provider communication training program alone, versus that same training plus a collaborative quality improvement program for practice leaders. HPV vaccination prevents over 35,000 cancer cases per year in the US, yet initiation rates remain below target, partly because clinicians lack effective communication skills to address parental hesitancy. Eligible participants are children aged 9–17 who present for a well-child visit at a participating practice and have not yet received the HPV vaccine. Practices — not individual participants — are randomized to one of three arms (two interventions or usual care), and vaccination rates are tracked over a 12-month intervention period. This summary was prepared using AI to help patients understand the study in plain language.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALSTOP-HPV-Online

Approximately one third of practices within a participating health system will be randomized to receiving the STOP-HPV-Online intervention.

BEHAVIORALSTOP-HPV-LC

Approximately one third of practices within a participating health system will be randomized to receiving the STOP-HPV-LC intervention.


Locations(1)

AMGA

Alexandria, Virginia, United States

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NCT06831383


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