The STOP-HPV Scale Up Study

Authors
Category Primary study
Registry of TrialsClinicalTrials.gov
Year 2025
Human papillomavirus (HPV) causes 35,900 US cancer cases per year, 4,000 deaths, and $4 billion in cancer-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. In this study, we 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).
Epistemonikos ID: 2b037de18f7c8691c35c74d1e10aa3a206d86a53
First added on: Mar 01, 2025