Skip to main content
Clinical Trials/NCT03111251
NCT03111251
Completed
Not Applicable

Multi-component Interventions for Patients and Providers to Increase HPV Vaccination in a Network of Pediatric Clinics in Houston, TX

The University of Texas Health Science Center, Houston1 site in 1 country1,000 target enrollmentMarch 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Human Papillomavirus (HPV)
Sponsor
The University of Texas Health Science Center, Houston
Enrollment
1000
Locations
1
Primary Endpoint
Change in percent of HPV vaccination initiation
Status
Completed
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 1, 2015
End Date
February 28, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sally Vernon

◦Blair Justice, PhD Professorship in Mind-Body Medicine and Public Health and Director, Division of Health Promotion and Behavioral Sciences

The University of Texas Health Science Center, Houston

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change in percent of HPV vaccination initiation

Time Frame: baseline, 3 years

Study Sites (1)

Loading locations...

Similar Trials