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Clinical Trial Summary

This clinical trial studies how to improve the human papillomavirus (HPV) vaccination rate in young adults in Texas. This trial aims to learn more about how researchers and health care providers can increase HPV vaccination among college students.


Clinical Trial Description

PRIMARY OBJECTIVES: I. To determine the impact of addressing individual and system levels of influence on HPV vaccination initiation and completion rates. II. To gain insight into mechanisms of the intervention's efficacy, individual differences, and implementation of the intervention using mixed methods. OUTLINE: Participants are randomized to 1 of 6 groups. GROUP I: Participants receive standard Centers for Disease Control and Prevention (CDC) information about HPV vaccination. GROUP II: Participants receive video narratives about HPV vaccination. GROUP III: Participants receive written narratives about HPV vaccination. GROUP IV: Participants receive enhanced access to vaccination and standard CDC information about HPV vaccination. GROUP V: Participants receive enhanced access to vaccination and video narratives about HPV vaccination. GROUP VI: Participants receive enhanced access to vaccination and written narratives about HPV vaccination. After completion of study, participants are followed up at 3 and 9 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05057312
Study type Interventional
Source M.D. Anderson Cancer Center
Contact
Status Recruiting
Phase N/A
Start date March 1, 2022
Completion date July 31, 2026

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