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Recruiting NCT06890403

Can Stories Encourage the Elderly to Vaccinate? Combining Viewer-tailored Personal Narrative Videos With Informational Videos to Improve Vaccine Uptake Among Older Adults

No phase Interventional Vaccination

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Informational Animation Video, Personal Narrative Video.
Who it may be relevant to
Registry conditions: Vaccination. Basic parameters: from 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study will compare the use of informational videos only, personal story videos only, and the combination of both, to see which is most effective in increasing vaccination among older adults.

Interventions

  • Behavioral Informational Animation Video
    The informational animation video will also take several minutes and will cover human papillomavirus (HPV) disease, address specific concerns when identified, and the importance and safety of HPV vaccines.
  • Behavioral Personal Narrative Video
    Personal narrative videos will consist of someone describing the person's own personal experience with HPV. The investigators have a collection of videos of personal narratives from different people that the investigators have cut to approximate several minutes in length so the investigators can tailor the personal narratives to match each study participant's race/ethnicity and gender as closely as possible.

Primary outcome measures

  • Number of participants who receive vaccine [Time frame: 9-month follow-up]

Eligibility criteria

Inclusion criteria

  • U.S. adults aged 50 and older

Exclusion criteria

  • Participants who do not complete the survey
  • Participants who are unable or refuse to view and listen to videos on the participant's device

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

United States · 1 center
  • Ipsos — New York

Identifiers

NCT: NCT06890403 · IRB00032331

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗