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

Completed · Not applicable

Conditions studied: Human Papillomavirus (HPV)

In brief

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.

Key facts

Study ID

NCT03111251

Run by

The University of Texas Health Science Center, Houston

People needed

1000

Starts

2015-03-01

Expected to finish

2019-02-28

Last updated by the study team

2020-05-21

Who can join

Age: 11 and older, up to 17. Sex: any. Healthy volunteers: accepted.

You may qualify if…

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

You may not qualify if…

• Patient had completed the HPV vaccination series at baseline

Where it is running

• The University of Texas Health Science Center at Houston — Houston, Texas, United States

Full record on ClinicalTrials.gov

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