Actively Recruiting
PCOM2 - The Physician Communication Intervention, Version 2.0 for Linking the Provider Recommendation to Adolescent HPV Vaccine Uptake
Led by University of Colorado, Denver · Updated on 2024-08-26
120
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
Sponsors
U
University of Colorado, Denver
Lead Sponsor
U
University of Kansas Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating two versions of a provider communication intervention called PCOM to increase human papillomavirus (HPV) vaccination rates among adolescents aged 9 to 17 years. The study aims to develop and test a virtual version of the intervention (PCOM-Virtual) against the original in-person PCOM intervention (PCOM-Standard). This comparison will help determine whether the virtual method can be as effective and easier to spread widely, addressing low vaccination rates that leave many adolescents at risk for HPV-related cancers and diseases. The study involves two groups of primary care providers: one trained in the traditional in-person PCOM communication technique and the other trained through the newly developed virtual PCOM version. Both interventions teach providers to use a two-step communication approach: starting vaccine discussions with a presumptive style, followed by motivational interviewing to address parental hesitancy. The virtual version also aims to produce a ready-to-use intervention and user manual for easy adoption in clinical practices. Participants include adolescents receiving care at enrolled clinics and their providers. Researchers will track HPV vaccination initiation and completion in adolescents aged 11 to 12 and 13 to 17 years during the last 12 months of the 24-month intervention period. Data collection will include monitoring vaccination status and analyzing how practice, patient, and provider characteristics influence the interventions' effectiveness. The study runs until the end of 2026 and involves random assignment of providers to the two intervention groups with single masking.
CONDITIONS
Brief Title
PCOM2 - The Physician Communication Intervention, Version 2.0
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Parents must have an adolescent between 9 and 17 years old receiving adolescent care at an enrolled clinic
- All providers at participating study practices are eligible to participate
You will not qualify if you...
- Parents without an adolescent between 9 and 17 years old receiving care at an enrolled clinic
- Providers who do not work at participating study practices
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 24 months
Participants receive training through either an in-person provider communication intervention or a virtual version of the communication intervention aimed at improving HPV vaccination rates among adolescents.
Ongoing training and communication sessions during the 24 month intervention period
Duration - 12 months
Participants' adolescent vaccination initiation and completion status are assessed during the final 12 months of the intervention period to evaluate the efficacy of the interventions.
Assessments conducted based on routine clinical visits
Trial Site Locations
Total: 2 locations
1
University of Colorado Anschutz Medical Campus
Aurora, Colorado, United States, 80045
Actively Recruiting
2
University of Kansas Medical Center
Wichita, Kansas, United States, 67208
Actively Recruiting
Research Team
C
Christine Spina, MSPH
J
Julian Dedeaux
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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