Vaccine information provision

Last registered on December 09, 2025

Pre-Trial

Trial Information

General Information

Title
Vaccine information provision
RCT ID
AEARCTR-0017358
Initial registration date
December 02, 2025

Initial registration date is when the trial was registered.

It corresponds to when the registration was submitted to the Registry to be reviewed for publication.

First published
December 09, 2025, 7:23 AM EST

First published corresponds to when the trial was first made public on the Registry after being reviewed.

Locations

Region

Primary Investigator

Affiliation

Other Primary Investigator(s)

Additional Trial Information

Status
On going
Start date
2025-11-25
End date
2026-03-01
Secondary IDs
AsPredicted #260276
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
no information provided to avoid informing trial participants
External Link(s)

Registration Citation

Citation
Sacks, Daniel. 2025. "Vaccine information provision." AEA RCT Registry. December 09. https://doi.org/10.1257/rct.17358-1.0
Sponsors & Partners

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Experimental Details

Interventions

Intervention(s)
kept private to avoid biasing the study
Intervention (Hidden)
Four conditions, mutually exclusive.
1. Control: participants are told about a flu vaccine clinical trial and told the placebo arm severe adverse event (SAE) rate.
2. Industry info: Participants are additionally told that the SAE rate was not significantly higher in the vaccine arm.
3. Academic info: As control, plus people are told about an academic study of flu vaccine side effects, and informed that encouragement to vaccinate did not raise the SAE rate.
4. Personal info: Identical to the "academic info" arm, except participants are additionally told "the study participants were Prolific users who were not sure they wanted to get the flu vaccine."
Intervention Start Date
2025-12-02
Intervention End Date
2025-12-08

Primary Outcomes

Primary Outcomes (end points)
Our primary outcome variable is the believed, personal side effect rate of vaccination. We ask people to imagine they do not vaccinate tomorrow - what is the percentage point likelihood that they experience one or more severe adverse events over the next few days. This is the "posterior_no_vacc." Next we ask people the same question but imagining that they DO vaccinate. This is the "posterior_vacc" Our key dependent variable, the believed side effect rate, is posterior_vacc minus posterior_no_vacc.
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
various measures of vaccine intentions, plus persistence in beliefs and reliability of the provided information
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
kept private to avoid biasing the study
Experimental Design Details
sample consists of prolific participants who indicate vaccine hesitancy in a baseline survey.

vaccine hesitancy is defined as answering "do not intend to vaccinate" or "may or may not vaccinate" whe nasked about flu vaccination status for the 2025-26 season.

Participants are recruited in a baseline survey that runs for 7 days or until screening 8000 participants. All vaccine hesitant participants invited to the main survey, with a target sample size of 4000. Main survey will run for 7 days or until we hit the target.

In the main survey, participants are randomized to one of the four arms. We will analyze the experiment with OLS regression of outcome on treatment arm indicators and covariates.

Covariates:
- indicators for prior belief levels (which are elicited in multiple choice questions)
- indicators for vaccine intent (may or may not vs. do not intend), measured in screening survey
- indicators (separate) for demographics: age, gender, education, income, race, ethnicity, political views
- indicators for prior vaccine experience: prior flu vacc, prior covid vacc, reporting experiencing prior adverse event from covid vaccine, reporting experiencing prior adverse event from flu vaccine
- indicators for reported trust in government sources (current) and flu vaccine indicators for health conditions.

Randomization Method
qualtrics randomizer
Randomization Unit
individual
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
4000
Sample size: planned number of observations
4000
Sample size (or number of clusters) by treatment arms
4000
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
Simulations on pilot data indicate an MDE of just over 2.9 percentage points, with 80% power. The SD of the unadjusted outcome metric is 31.6 and the mean is 19.6, so the MDE is 15% of the mean.
IRB

Institutional Review Boards (IRBs)

IRB Name
University of Wisconsin IRB
IRB Approval Date
2025-10-27
IRB Approval Number
2025-1542
Analysis Plan

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Post-Trial

Post Trial Information

Study Withdrawal

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Intervention

Is the intervention completed?
No
Data Collection Complete
Data Publication

Data Publication

Is public data available?
No

Program Files

Program Files
Reports, Papers & Other Materials

Relevant Paper(s)

Reports & Other Materials