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Clinical Trial Summary

The primary objectives of this study are to increase HPV vaccination initiation and 3-dose completion among pediatric, adolescent, and young adult (PAYA) cancer survivors


Clinical Trial Description

PAYA cancer survivors are 2.8 times more likely to develop a secondary human papillomavirus (HPV)-associated cancer than the general population. Unfortunately, HPV vaccination coverage among PAYA cancer survivors is even lower than that in the general population. Provision of adequate vaccine information and instructions for timing of vaccination post-treatment is associated with an increased intention to vaccinate. Nonetheless, research show a minority of cancer care teams specifically discuss HPV vaccination with PAYA cancer survivors and their caregivers. The purpose of this study is to test the efficacy of an oncologist- and clinic-level intervention and the additional effect of a patient-level app-based intervention to improve initiation and 3-dose completion of the HPV vaccine series. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05665543
Study type Interventional
Source Masonic Cancer Center, University of Minnesota
Contact Deanna Teoh, MD, MS
Phone 612-625-6503
Email dkteoh@umn.edu
Status Recruiting
Phase N/A
Start date July 24, 2023
Completion date August 2026

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