Multi-component Interventions to Increase HPV Vaccination in a Network of Pediatric Clinics

Not Applicable

Completed

• Conditions: Human Papillomavirus (HPV)

• Registration Number: NCT03111251
• Lead Sponsor: The University of Texas Health Science Center, Houston

Brief Summary

The purpose of the study is to determine the comparative effectiveness of a provider-only intervention and a parent plus provider intervention to increase initiation of HPV vaccination among male and female patients ages 11-17 in a large pediatric clinic network in the greater Houston area. The hypothesis is that HPV vaccine initiation will be higher in clinics randomized to the parent plus provider intervention compared with clinics randomized to the provider-only intervention.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-03-01
• Study First Submitted: 2017-04-06
• Study First Submitted QC: 2017-04-06
• Study First Posted: 2017-04-12
• Primary Completion: 2019-02-28
• Study Completion: 2019-02-28
• Status Verified: 2020-05
• Last Update Submitted: 2020-05-20
• Last Update Posted: 2020-05-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1000

Inclusion Criteria

• Patient at a Texas Children's Pediatrics clinic
• Patient had not initiated the HPV vaccination series at baseline

Exclusion Criteria

• Patient had completed the HPV vaccination series at baseline

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change in percent of HPV vaccination initiation	baseline, 3 years

Trial Locations

Locations (1)

The University of Texas Health Science Center at Houston; 🇺🇸 Houston, Texas, United States