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Recruiting NCT07236034

ARISe at UMass Chan

No phase Interventional Vaccination Vaccination Promotion

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: Exposure to source and message content.
Who it may be relevant to
Registry conditions: Vaccination, Vaccination Promotion. Basic parameters: from 18 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 →
Official title

ARISe at UMass Chan: Remote Eye Tracking Study of Vaccine Messaging in Rural Populations

Overview

The goal is to identify the most impactful strategies for capturing attention and enhancing effectiveness of vaccine promotion messages. This will be done using an online survey that employs remote eye-tracking and self report measures to evaluate response to sample vaccine promotion social media content in rural populations in New England. Participants will be randomly assigned into one of 14 conditions in a 2(source: expert vs. influencer) by 7 (themes: constructs from 7C Vaccine Framework) experiment and view sample messages and then answer questions about their attitudes and beliefs while being monitored for eye-tracking.

Interventions

  • Behavioral Exposure to source and message content
    Within each arm, participants will be exposed to two messages each of which are delivered by the same source (peer or professional) and have message content related to one of the 7C Constructs.

Primary outcome measures

  • Source credibility [Time frame: Immediately after viewing each message]
  • Perceived Message Effectiveness [Time frame: Immediately after viewing each message]
  • Visual attention [Time frame: During message viewing ( immediately post-randomization, prior to completion of post-message survey)]
  • Message reactance [Time frame: Immediately after viewing each message]
  • Information sharing intentions [Time frame: Immediately after viewing each message]
Secondary outcome measures (1)
  • Vaccine perceptions [Time frame: Assessed at baseline (prior to message exposure) and immediately post-intervention (after message exposure)]

Eligibility criteria

Inclusion criteria

  • Age 18+
  • Living in New England state (CT, MA, ME, NH, VT RI) in a zip code as defined by each individual state's definition of rural
  • Able to read and write in English
  • Access to an internet connected computer or laptop with a web-camera

Exclusion criteria

  • N/A

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
Factorial
Masking
Double blind
Primary purpose
Health services research

Study locations

United States · 1 center
  • University of Massachusetts Chan Medical School — Worcester

Identifiers

NCT: NCT07236034 · STUDY00002075 · 1U48DP006883-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗