Parents' HPV Stories

Part of paid clinical trials in Lexington, Kentucky.

Sponsor
Anne E Ray
Study ID
NCT06704308
Status
Not Yet Recruiting

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Conditions

  • HPV Vaccination

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Web Application — BEHAVIORAL
    A web application for vaccine-hesitant parents and their teens with brief, 90-second narrative videos and tailored, motivational content
  • Provider Elaborated Prompts — BEHAVIORAL
    A component for providers that suggests elaborated prompts to be used with parents that align with the content of the web application, are tailored to parent concerns, and are motivational in nature

Study Details

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.

Key Dates

Start date
May 31, 2026
Status verified
Dec 2025
Primary completion
Nov 30, 2026
Completion
Nov 30, 2026

Study Design

Enrollment
58 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION

Arms

  • Experimental: Parents' Stories Web Application + Provider Elaborated Prompts
    Participating parents will be asked to navigate a web application that consists of (a) brief, 90-second narrative videos that encourage parent-provider communication about the vaccine and (b) personalized feedback to parents that is tailored to provide educational content in response to their concerns and be motivational in nature. Providers will provide elaborated prompts related to the vaccine when meeting with parents tailored to their concerns.

Primary Outcome Measure

Change in HPV Vaccine Hesitancy Scale score [ Time Frame: From pretest to posttest (up to two weeks) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of KentuckyLexingtonKentucky40506
Anne E Ray, PhD
[email protected]
859-218-4944

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By research site
University of Kentucky· Lexington, KY

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