CompletedNot Applicable

Culturally Tailored HPV Psychoeducational Multimedia Intervention

United States63 participantsStarted 2024-05-02

Plain-language summary

Community members ages 18 - 45 years old from the El Paso, Texas, U.S.-Mexico Border Region will be recruited to compare psychoeducational multimedia interventions focused on the human papillomavirus (HPV). Our hypothesis is that adults who view culturally tailored multimedia stories encouraging HPV vaccination will report higher vaccine uptake rates.

Who can participate

Age range

18 Years – 45 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adults between the ages 18 and 45 years old * Adults who have not completed the HPV vaccine series (unvaccinated or under-vaccinated) * Adults currently living or working in El Paso County, Texas Exclusion Criteria: * Adults who participated in Phases I or II of the larger research project \[cross-sectional phases\] * Adults younger than 18 years of age * Adults older than 45 years of age * Adults that do not reside, plan to live or work in El Paso County, Texas, within the next 12 months after the start of the intervention * Adults who are unable to participate in the full study intervention and follow-up time-points * Adults who cannot complete study participation and activities in either the English or Spanish languages.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

HPV Vaccination Status

Timeframe: Baseline (pre-assessment), 1 month post-intervention

HPV Vaccine Intention Score

Timeframe: Baseline (pre-assessment), immediately post-intervention (0 months), 1 month post-intervention.

Trial details

NCT IDNCT06098690

SponsorUniversity of Texas, El Paso

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-08-28

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