CClinicalTrials.gg
RecruitingNCT07236034ARISeUpdated Jul 7, 2026

ARISe at UMass Chan

An interventional study of Exposure to source and message content in Vaccination and Vaccination Promotion, sponsored by University of Massachusetts, Worcester. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-07.

Sponsored by University of Massachusetts, Worcester · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Started Dec 2025; still recruiting 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
700
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Vaccination
  • Vaccination Promotion

Keywords

  • Message perceptions
  • Vaccination
  • Immunization
03

In context

Lead sponsor

University of Massachusetts, Worcester is the lead sponsor of 288 studies on the registry; 54 are open to participants now.

Of its 25 completed or terminated interventional studies of FDA-regulated products, 18 (72%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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

Exclusion Criteria:

  • N/A
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Double (Participant, Investigator)
Enrollment
700 participants (estimated)

Study arms

  • Experimental
    Arm 1: Peer message, 7C Construct 1

    This arm will include messages with a "peer" influence as the source and the construct of "confidence" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 2: Professional source, 7C Construct 1

    This arm will include messages with a "professional" influencer as the source and the construct of "confidence" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 3: Peer message, 7C Construct 2

    This arm will include messages with a "peer" influence as the source and the construct of "complacency" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 4: Professional message, 7C Construct 2

    This arm will include messages with a "professional" influence as the source and the construct of "complacency" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 5: Peer message, 7C Construct 3

    This arm will include messages with a "peer" influence as the source and the construct of "constraints" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 6: Professional message, 7C Construct 3

    This arm will include messages with a "professional" influencer as the source and the construct of "constraints" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 7: Peer message, 7C Construct 4

    This arm will include messages with a "peer" influencer as the source and the construct of "calculation" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 8: Professional message, 7C Construct 4

    This arm will include messages with a "professional" influencer as the source and the construct of "calculation" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 9: Peer message, 7C Construct 5

    This arm will include messages with a "peer" influencer as the source and the construct of "collective responsibility" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 10: Professional message, 7C Construct 5

    This arm will include messages with a "professional" influencer as the source and the construct of "collective responsibility" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 11: Peer message; 7C Construct 6

    This arm will include messages with a "peer" influencer as the source and the construct of "compliance" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 12: Professional message, 7C Construct 6

    This arm will include messages with a "professional" influencer as the source and the construct of "compliance" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 13: Peer message, 7C Construct 7

    This arm will include messages with a "peer" influencer as the source and the construct of "conspiracy" as the message.

    Behavioral: Exposure to source and message content

  • Experimental
    Arm 14: Professional message, 7C Construct 7

    This arm will include messages with a "professional" influencer as the source and the construct of "conspiracy" as the message.

    Behavioral: Exposure to source and message content

Interventions

  • BehavioralExposure 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.

06

What researchers measure

Primary outcomes

  1. Source credibility

    Participants' perception of the credibility of the message source will be assessed using a 7-point Likert scale measured across four items. Participants will be asked to rate the following four items on this scale: To what extent do you believe the source of the message to be… (1=not at all, 7=very much so) 1. Fair 2. Accurate 3. Telling the whole story 4. Trustworthy Unit of measure: Scale score 1-7, mean

    Time frame: Immediately after viewing each message

  2. Perceived Message Effectiveness

    Perceived message effectiveness will be measured using six items (worth remembering, grabs attention, powerful, informative, meaningful, convincing), each rated on a 7-point Likert scale. The outcome will be the mean of these six ratings for each participant, then averaged by experimental condition. To what extent is… (1=not at all, 7=very much so) 1. The message worth remembering 2. The message grabs attention 3. This message powerful 4. This message informative 5. This message meaningful 6. This message convincing Unit of Measure: Scale score (1-7, mean across items)

    Time frame: Immediately after viewing each message

  3. Visual attention

    Visual attention, quantified as mean dwell time in milliseconds, will be measured using remote eye-tracking while participants view vaccine promotion messages. Dwell time will be calculated for pre-specified Areas of Interest (AOIs) during the message viewing period. Higher dwell times indicate greater visual attention to the AOIs. Unit of measure: mean dwell time in milliseconds per message

    Time frame: During message viewing ( immediately post-randomization, prior to completion of post-message survey)

  4. Message reactance

    Reactance will be assessed using four items (irritated, angry, annoyed, aggravated), rated 0 ("None of this feeling") to 4 ("A great deal of this feeling"). The mean reactance score will be calculated for each participant. How much did this message make you feel the following way? Response options: 0 (None of this feeling) to 4 (A great deal of this feeling). 1. Irritated 2. Angry 3. Annoyed 4. Aggravated Unit of Measure: Scale score (0-4, mean across items)

    Time frame: Immediately after viewing each message

  5. Information sharing intentions

    Description: Assessed with 6 items regarding interpersonal and online sharing, rated 1 (Strongly disagree) to 5 (Strongly agree). The mean score across items will be reported per participant and per condition. Rate with the following statements on a scale from 1 (Strongly disagree) to 5 (Strongly agree). Interpersonal setting 1. I would be willing to share this information with others. 2. I would talk with others about this message. 3. I would point others in a direction where they could read this message. Online setting 4. I would be willing to post a link to this information on my social media. 5. I would like a social media post with this information. 6. I would share a social media post with this information. Unit of Measure: Scale score (1-5, mean across items)

    Time frame: Immediately after viewing each message

Secondary outcomes

  1. Vaccine perceptions

    Vaccine perceptions will be measured using an 8-item scale, administered pre- and post-message exposure. Items are rated from 1 (Strongly disagree/very negative) to 7 (Strongly agree/very positive). Higher scores indicate more positive vaccine perceptions. The outcome will be the mean change in score from pre- to post-exposure. Unit of Measure: Scale score (1-7, mean change)

    Time frame: Assessed at baseline (prior to message exposure) and immediately post-intervention (after message exposure)

07

Study locations

1 of 1 sites recruiting
  • University of Massachusetts Chan Medical School
    Worcester, Massachusetts 01605, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Per the data management plan, datasets and codebooks will be provided to individual researchers upon reasonable request.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07236034
Lead sponsor
University of Massachusetts, Worcester
Responsible party
Grace Ryan (Assistant Professor, University of Massachusetts, Worcester) — Principal investigator
First posted
Nov 19, 2025
Start date
Dec 1, 2025
Primary completion
Sep 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Jul 7, 2026

Study contacts

Grace W Ryan, PhD, MPH
Contact
grace.ryan1@umassmed.edu
508-859-0179
Grace W Ryan, PhD, MPH
principal investigator · University of Massachusetts, Worcester

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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