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.
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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