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.
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change in HPV Vaccine Hesitancy Scale score
Timeframe: From pretest to posttest (up to two weeks)
Change Human Papillomavirus Knowledge Questionnaire score
Timeframe: From pretest to posttest (up to two weeks)
Change in intent to discuss HPV vaccine with provider
Timeframe: From pretest to posttest (up to two weeks)
Change in HPV vaccine intent
Timeframe: From pretest to posttest (up to two weeks)
Change in self-reported HPV vaccination and related provider recommendations
Timeframe: from screening to posttest (up to two weeks)
Change in Reasons Not to Vaccinate score
Timeframe: Pretest only