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Clinical Trials/NCT07648953
NCT07648953RecruitingNot Applicable

Microvideos for Improving HPV Vaccination Among Childhood Cancer Survivors

University of Utah1 site in 1 country55 target enrollmentStarted: August 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
55
Locations
1
Primary Endpoint
Feasibility of Microvideo education

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 26 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Eligible participants include cancer survivors who are currently ages 18-26 years and who were diagnosed with childhood cancer (ages 0-26 at diagnosis) in the past ten years.
  • •Currently use Facebook or willing to create a Facebook account to use for the duration of the study.
  • •At the time of enrollment, have not completed all recommended doses of the HPV vaccine.

Exclusion Criteria

  • •Unable to speak and understand English.
  • •Participants who take part in the Aim 1 focus groups will be ineligible for the Aim 2 social media group.
  • •Participants who are fully vaccinated for HPV will be ineligible as the goal of Aim 2 is to evaluate the feasibility of the social media campaign for improving vaccine intention among HPV unvaccinated individuals.

Arms & Interventions

HPV Vaccination Education

Other

Microvideos are designed to be <2 minutes long and to address key information on a topic in an engaging and concise manner. HPV vaccine education will be provided to unvaccinated emerging adult survivors of childhood cancer through a pilot quasi-experimental social media intervention.

Intervention: Microvideos: HPV Vaccination Education (Behavioral)

Outcomes

Primary Outcomes

Feasibility of Microvideo education

Time Frame: up to 4 weeks

Feasibility will be defined as ≥80% of participants completing the intervention and study surveys.

Secondary Outcomes

  • Acceptability of Microvideo Education(up to 4 weeks)
  • Satisfaction Acceptability of Microvideo Education(up to 4 weeks)
  • HPV Vaccine Intention(up to 4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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