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NCT04469569Completed

Provider-Focused Intervention for Maximizing HPV Vaccine Uptake in Young Cancer Survivors

Implementation of a Provider-Focused Intervention for Maximizing HPV Vaccine Uptake in Young Cancer Survivors Receiving Follow-Up Care in Pediatric Oncology Practices: A Cluster-Randomized Trial

Source: ClinicalTrials.gov · Last updated 3 Aug 2026

Brief summary (registry, in English)

The focus of this research is on increasing the uptake of the human papillomavirus (HPV) vaccine in young cancer survivors, a vulnerable population at high risk for developing new cancers (such as cervical and anal cancer) caused by persistent HPV infection. An effective vaccine exists that can prevent these cancers, but HPV vaccine uptake is low among young cancer survivors. This research will evaluate the effectiveness and implementation of an evidence-based intervention, adapted for use by healthcare providers in pediatric oncology clinics, to increase the uptake of HPV vaccine among young cancer survivors 9-17 years of age. Results of this research will provide important information that can be used to implement new strategies to increase the uptake of the HPV vaccine among young cancer survivors.

Status (registry)
Completed
Study type
Interventional
Enrollment
8120 (actual)
First submitted
9 Jul 2020
Start date
1 Feb 2021
Primary completion date
26 Jan 2025
Lead sponsor
University of Alabama at Birmingham
NCT number
NCT04469569

What you commit to

  • Study type: Interventional
  • Participants enrolled: 8120
  • From 1 Feb 2021 to the primary completion date, 26 Jan 2025
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • N/A

Who the study is looking for

  • HEALTHCARE PROVIDERS (ONCOLOGISTS, ADVANCED PRACTICE PROVIDERS)
    • ≥18y of age
    • Care for cancer survivors seen in the targeted clinic who are age 9-17y, ≥1y off-therapy, and reside in the state where clinic is located
    • Licensed to order vaccines
    • Willing to complete surveys and/or interviews
  • CHILDHOOD CANCER SURVIVORS
    • 9-17y of age
    • ≥1y following completion of cancer therapy
    • Reside in the state where clinic is located
    • Receive follow-up care (in person or via telehealth) at the participating sites

Age in the registry: 9 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesUnknown status
Baylor College of Medicine
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
University of Minnesota
Coordinator of this site? Confirm its status
MinneapolisUnited StatesUnknown status
Oregon Health and Science University
Coordinator of this site? Confirm its status
PortlandUnited StatesUnknown status
Wake Forest University Health Sciences
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.