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Provider-Focused Intervention for Maximizing HPV Vaccine Uptake in Young Cancer Survivors

Helping providers increase HPV vaccine rates in young cancer survivors.

Recruiting
9 years and older
All
Phase N/A

Study Focus: This study aims to improve the uptake of the HPV vaccine (which helps prevent cancers caused by the human papillomavirus) in young cancer survivors aged 9-17 who are at higher risk for new cancers. The study evaluates an intervention called HPV-PROTECT used by healthcare providers in pediatric oncology clinics.

HPV-PROTECT Intervention: The intervention has three parts: 1) Provider Communication Training to better recommend the vaccine, 2) Assessment and Peer Feedback/Coaching to improve communication skills, and 3) a Provider Toolkit to help providers with vaccine-related information. It aims to increase healthcare providers' knowledge and skills in recommending the HPV vaccine and decrease barriers to vaccine uptake.

  • Duration & Visits: Participation includes completing surveys and/or interviews.
  • Eligibility: Targets healthcare providers who treat cancer survivors, and young cancer survivors aged 9-17.
  • Compensation: Not specified, but participants contribute to valuable research for improving health outcomes.

This study will offer insights into increasing HPV vaccine rates, potentially leading to broader use in clinics.

Study details
    Papillomavirus Vaccines

NCT04469569

University of Alabama at Birmingham

13 December 2024

Step 1 Get in touch with the nearest study center
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Learn more about clinical trials

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

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