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Parents' HPV Stories

NCT06704308 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2026-04-06

No results posted yet for this study

Summary

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.

Conditions

  • HPV Vaccination

Interventions

BEHAVIORAL

Web Application

A web application for vaccine-hesitant parents and their teens with brief, 90-second narrative videos and tailored, motivational content

BEHAVIORAL

Provider Elaborated Prompts

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

Sponsors & Collaborators

  • Real Prevention, LLC

    collaborator INDUSTRY

  • Merck Institute for Therapeutic Research

    collaborator UNKNOWN

  • Anne E Ray

    lead OTHER

Principal Investigators

  • Anne E Ray, PhD. · University of Kentucky

  • Aaron Kruse-Diehr, PhD · University of Kentucky

  • Michael Hecht, PhD · Real Prevention, LLC

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-05-31
Primary Completion
2026-11-30
Completion
2026-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06704308 on ClinicalTrials.gov