Multi-component Interventions to Increase HPV Vaccination in a Network of Pediatric Clinics
Purpose
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.
Condition
- Human Papillomavirus (HPV)
Eligibility
- Eligible Ages
- Between 11 Years and 17 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- Yes
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
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Prevention
- Masking
- None (Open Label)
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
Experimental Provider-only intervention |
New provider- and system-level evidence-based strategies for increasing HPV vaccination rates are being implemented throughout the entire clinic network. This includes provider assessment and feedback, provider reminders, provider education, and patient reminders. |
|
Experimental Provider plus parent intervention |
Clinics randomized to the provider plus parent intervention will receive both the provider intervention and the parent education intervention. |
|
More Details
- Status
- Completed
- Sponsor
- The University of Texas Health Science Center, Houston