RECRUITING

The HPV 9-10 Trial: Early Initiation of HPV Vaccination

Conditions

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

Every year, thousands of Americans die from cancers related to human papillomavirus (HPV). The vast majority of those deaths could be prevented with a safe and effective vaccine, yet many parents choose not have their children vaccinated when it is recommended at age 11 or 12. In this study, we will examine in a randomized trial whether earlier initiation of the vaccine at age 9-10 years will result in less parental refusal and higher rates of full vaccination at younger ages, before early sexual activity begins.

Official Title

The HPV 9-10 Trial: Early Initiation of HPV Vaccination

Quick Facts

Study Start:2019-12-23
Study Completion:2025-04-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04722822

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Practices in Metro Denver, Colorado and Metro Los Angeles, California (specifically UCLA medical clinics and clinics affiliated with Children's Hospital of Orange County)
  2. * Practices that have at least 60% of providers agree to participate
  3. * Practices do not currently recommend HPV at 9-10 years.
  4. * Practice must have at least 100 eligible patients age 9-13 years
  1. * Practices with less than 100 eligible patients age 9-13 years
  2. * Practices currently routinely recommend HPV vaccine at 9-10 years.
  3. * Practices where less than 60% of providers agree to participate in the study.

Contacts and Locations

Study Contact

Alison Saville, MPH, MSW
CONTACT
720-257-4406
alison.saville@cuanschutz.edu

Principal Investigator

Allison Kempe, MD, MPH
PRINCIPAL_INVESTIGATOR
University of Colorado, Denver

Study Locations (Sites)

University of California at Los Angeles
Los Angeles, California, 90095
United States
University of Colorado
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • Allison Kempe, 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 Date2019-12-23
Study Completion Date2025-04-01

Study Record Updates

Study Start Date2019-12-23
Study Completion Date2025-04-01

Terms related to this study

Additional Relevant MeSH Terms

  • HPV