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A Vaccine Promotion Package (TweenVax) to Improve Adolescent HPV Vaccination, TweenVax Trial

Join the TweenVax Trial to boost HPV vaccination rates for teens!

Recruiting
9 years and older
All
Phase N/A

This study tests a new way, called **TweenVax**, to promote the HPV vaccine for kids aged 9-12. The **HPV vaccine** helps prevent certain types of cancers caused by the Human Papillomavirus. The **TweenVax** program aims to improve vaccination rates by offering more information and support to doctors, staff, parents, and kids. The study is comparing three different approaches: one group gets the full TweenVax program, another gets parts of it, and the last group continues with regular vaccination practices. The goal is to see if the TweenVax approach helps more kids finish their vaccinations by age 13. Doctors' offices taking part in the study will be followed for up to a year.

  • The study lasts about 9 months, plus follow-up for a year.
  • Participants are kids aged 9-12 who haven't started the HPV vaccine yet.
  • Doctors' offices must have electronic records and see enough kids to join.
Study details
    Human Papillomavirus-Related Carcinoma

NCT07104240

Emory University

10 October 2026

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Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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