Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Stories to Prevent HPV Cancers

Official title: Stories to Prevent (StoP) HPV Cancers: A Communication Intervention to Increase HPV Vaccination Among Diverse Populations.

Run by Milton S. Hershey Medical Center · NCT06808776 · Data updated 2026-11-12

We will try short videos of local cancer survivors telling their HPV stories to see if parents of 9- to 12-year-olds are more likely to start the HPV vaccine for their children.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment200 (estimated)
SponsorMilton S. Hershey Medical Center
Academic / other
Locations1 site (Hershey, Pennsylvania)
StatusRecruiting
StartedNovember 18, 2025
Main results expectedOctober 30, 2026
Study endsMarch 31, 2027
Registry record updatedFebruary 24, 2026
Trial IDNCT06808776 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Parents or legal guardians of 9- to 12-year-old children who receive primary care at Penn State Health, whose child has not initiated the HPV vaccine, who read English or Spanish, and who have an email address and access to a mobile phone, tablet, or computer.

Probably not a fit

Parents of children who have already received or started the HPV vaccine, people without access to email or a compatible device, non-English/Spanish speakers, or those not receiving care at Penn State Health are unlikely to be eligible or to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial will enroll 200 parents of 9- to 12-year-old children who have not started the HPV vaccine and randomize them 1:1 to receive either a brief survivor-narrative video or a placebo video one week before their child's primary care visit. The survivor videos feature local cancer survivors describing their HPV-related diagnoses and recommending vaccination, while control participants view a healthy-eating tips video of similar length. The primary outcome is HPV vaccine initiation at the wellness visit (first dose received), and the study will also measure parents' cognitive and emotional reactions—such as perceived risk, hope, and anticipated regret—as theory-based mediators. Materials are delivered via digital channels (email, patient portal, or mobile device) and participants are recruited from Penn State Health pediatric and family medicine clinics.

Why it matters

Potential benefit: If successful, the intervention could boost HPV vaccine starts among 9- to 12-year-olds by motivating parents before clinic visits and thereby help prevent future HPV-related cancers.

How similar studies have gone: Previous research indicates narrative messages can improve vaccine attitudes and sometimes uptake, but findings are mixed and pre-visit survivor-video interventions are a relatively novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Parent/guardian of a 9-12 year old receiving primary care at a Penn State Health clinic
* Their child has not previously received or initiated the HPV vaccine
* Is able to read and understand spoken English or Spanish
* Has a valid email address and access to a mobile phone, table, desktop or laptop computer to engage in the intervention

Exclusion Criteria:

* Parent of guardian is less than 18 years of age
* Unable to read and understand spoken English or Spanish
* Does not have access to a mobile phone, table, desktop or laptop computer

Where it's running

  • Penn State Health
    Hershey, Pennsylvania, United States
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.