About this trial
The goal of this clinical trial is to evaluate the feasibility of intervention implementation in two clinics in rural KY, and its preliminary efficacy with regards to increasing vaccine confidence in a sample of vaccine hesitant parents.
Hypothesis: Parents will report increased vaccine confidence scores post-intervention.
Data from this study will provide preliminary data for a larger scale evaluation of the intervention.
Participants will be asked to complete surveys, view a web-based intervention and then visit with their child's healthcare provider.
Eligibility criteria
Qualifiers
status as a mother or female guardian of an 11-17-year-old adolescent
status as a U.S. resident
self-reported ability to read English
self-reported HPV vaccine hesitant using established methodology
Disqualifiers
None
Trial design
Treatments tested in this trial
- Web Application
- Provider Elaborated Prompts
Treatment groups
Sponsors and collaborators
Anne E Ray
Lead sponsor
University of Kentucky
Sponsor institution
Real Prevention, LLC
Collaborator
Merck Institute for Therapeutic Research
Collaborator