55 Participants NeededMy employer runs this trial

Microvideos for HPV Vaccination

EW
Overseen ByEcho Warner, MPH, PhD, SB
Age: 18 - 65
Sex: Any
Trial Phase: Academic
Sponsor: University of Utah
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This exploratory mixed-methods study aims to examine receipt of treatment and decision-making among rural cancer patients in Utah. Guided by Conceptual Model of Healthcare Access, the study will integrate, survey and cancer registry data with patient interviews to better understand how travel burden, socioeconomic conditions, health literacy, and other contextual factors shape treatment location and access to care . While the setting of this research is specific to Utah, a state with vast rural regions and only one National Cancer Institute (NCI)-designated cancer center, the findings may inform policy and practice improvements in other states with similar geographic and healthcare infrastructure. Thus, the study has potential relevance for advancing rural cancer equity nationwide.

Understanding how rural cancer patients make treatment decisions is essential to addressing persistent disparities in cancer care access and outcomes. While geographic barriers and structural inequities are well-documented, less is known about the individual and contextual factors that shape patients' choices about where and how to receive treatment. This mixed-methods study will examine receipt of treatment, decision-making, and patient experience among rural cancer patients in Utah, with attention to travel burden, referral pathways, health literacy, and perceived barriers to care.

Who Is on the Research Team?

EW

Echo Warner, MPH, PhD, SB

Principal Investigator

Huntsman Cancer Institute

Are You a Good Fit for This Trial?

This trial is for cancer survivors aged 18-26 who were diagnosed with childhood cancer in the past ten years, use or are willing to use Facebook, and have not finished all recommended HPV vaccine doses. Participants must speak English and cannot already be fully vaccinated for HPV.

Inclusion Criteria

I use Facebook or am willing to create an account for the study.
I am 18-26 and was diagnosed with childhood cancer in the last 10 years.
I have not finished all recommended doses of the HPV vaccine.

Exclusion Criteria

Unable to speak and understand English
I have not received the full HPV vaccine series.
Participants who take part in the Aim 1 focus groups are ineligible for the Aim 2 social media group

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Intervention

Participants receive HPV vaccine education through microvideos as part of a pilot quasi-experimental social media intervention

4 weeks
Virtual engagement through social media

Follow-up

Participants are monitored for feasibility, acceptability, and satisfaction of the microvideo education

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Microvideos: HPV Vaccination Education

Trial Overview

The study tests whether short educational videos about the HPV vaccine shared on Facebook can help increase vaccination rates among young adult cancer survivors. The research uses surveys and interviews to understand decision-making around vaccination.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: HPV Vaccination EducationExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Utah

Lead Sponsor

Trials
1,169
Recruited
1,623,000+

Prevent Cancer Foundation

Collaborator

Trials
7
Recruited
1,500+

Huntsman Cancer Institute

Collaborator

Trials
14
Recruited
7,700+