RECRUITING

PCOM2 - The Physician Communication Intervention, Version 2.0

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Poor quality of primary care providers' vaccine recommendations lead to low adolescent human papillomavirus vaccination rates and hundreds of thousands of adolescents unnecessarily at risk for HPV-associated cancers and diseases. Though a previous provider communication intervention, called PCOM, was found to be effective for increasing adolescent HPV vaccination in primary care, its dissemination is limited by the need for significant research team involvement to teach providers how to use the intervention's components. To address this, investigators propose to develop and test a virtual version of PCOM, use mixed methods to assess contextual factors affecting its use compared to the original PCOM intervention, and develop an optimized version of PCOM for broad dissemination to increase adolescent HPV vaccination nationally.

Official Title

PCOM2 - The Physician Communication Intervention, Version 2.0" for "Linking the Provider Recommendation to Adolescent HPV Vaccine Uptake"

Quick Facts

Study Start:2023-11-15
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05336240

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:9 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Parents: Have an adolescent between the ages of 9-17 years old and receiving adolescent care at an enrolled clinic
  2. * Providers: All providers at participating study practices will be eligible to participate.
  1. * Parents: Does not have an adolescent between the ages of 9-17 years old and is not receiving adolescent care at an enrolled clinic
  2. * Providers: Providers who are not at participating study practices

Contacts and Locations

Study Contact

Christine Spina, MSPH
CONTACT
303.724.0906
CHRISTINE.BABBEL@CUANSCHUTZ.EDU
Julian Dedeaux
CONTACT
jdedeaux@kumc.edu

Principal Investigator

Sean O'Leary, MD, MPH
PRINCIPAL_INVESTIGATOR
University of Colorado, Denver

Study Locations (Sites)

University of Colorado Anschutz Medical Campus
Aurora, Colorado, 80045
United States
University of Kansas Medical Center
Wichita, Kansas, 67208
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • Sean O'Leary, MD, MPH, PRINCIPAL_INVESTIGATOR, University of Colorado, Denver

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-11-15
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2023-11-15
Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

  • Immunization
  • Provider Communication
  • HPV Prevention

Additional Relevant MeSH Terms

  • HPV Infection
  • Preventive Health Services