Correcting COVID-19 Risk Misperceptions via Information Provision

Last registered on January 06, 2026

Pre-Trial

Trial Information

General Information

Title
Correcting COVID-19 Risk Misperceptions via Information Provision
RCT ID
AEARCTR-0017584
Initial registration date
January 04, 2026

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
January 06, 2026, 7:20 AM EST

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

Locations

Region

Primary Investigator

Affiliation
University of Tokyo

Other Primary Investigator(s)

PI Affiliation
University of Tokyo
PI Affiliation
University of Tokyo
PI Affiliation
University of Tokyo
PI Affiliation
Hitotsubashi University

Additional Trial Information

Status
Completed
Start date
2023-04-25
End date
2023-04-27
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
We conducted an information provision experiment in April 2023 in Japan to investigate how different types of information affect people's subjective assessment of COVID-19 related risks. The majority of respondents overestimate infection and fatality risks. Recent infection-related statistics lower risk perceptions if presented in percentage, but do not lower them if presented in levels. Providing pessimistic outlooks raises risk perceptions. We also find substantial heterogeneity in the response to information provision across various individual characteristics, such as age, gender, education, marital status, health status, COVID-19-related experiences, and vaccination status.
External Link(s)

Registration Citation

Citation
Chiba, Asako et al. 2026. "Correcting COVID-19 Risk Misperceptions via Information Provision." AEA RCT Registry. January 06. https://doi.org/10.1257/rct.17584-1.0
Experimental Details

Interventions

Intervention(s)
Provide information about COVID-19 infection and fatality risks.
Intervention (Hidden)
Intervention Start Date
2023-04-25
Intervention End Date
2023-04-27

Primary Outcomes

Primary Outcomes (end points)
Respondents' perceptions on COVID-19 infection and fataility risks
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
We divide participants into four groups. We do not provide Group 1---the control group---with any information. Meanwhile, we provide Group 2 with the recent total infected cases and deaths (referred to as ``level'' information). We provide Group 3 with the recent actual probabilities of getting infected and dying from COVID-19 once infected (``percentage'' information). Finally, we provide Group 4 with qualitative information about a possible future path of new infection (``qualitative'' information). Below is the exact wording for these three types of information:

Level information: From mid-March 2023 to mid-April 2023 in Japan, the total infected cases is 226,007. From April 2022 to March 2023 in Japan, the total deaths were 45,727.

Percentage information: From mid-March 2023 to mid-April 2023 in Japan, the actual infection rate is 0.18\%. From April 2022 to March 2023 in Japan, the actual fatality rate is 0.17\%.

Qualitative information: The number of new cases has been gradually increasing, and there is concern about the spread of infection after the holidays in May. On April 19, the expert group mentioned the possibility of a 9th wave, which would be larger than the 8th wave. Compared to the 6th and 7th waves (January-April 2022 and July-September 2022), the 8th wave (November 2022-February 2023) showed an increase in fatality rate.

After providing information about COVID-19, we ask participants about their perceptions of infection or fatality risks, namely, the subjective probability of being infected with COVID-19 within the next month and the probability of fatality if infected with COVID-19. For both infection and fatality risks, we present participants with the following response options: (1) less than 0.001%, (2) 0.001% to less than 0.01%, (3) 0.01% to less than 0.1%, (4) 0.1% to less than 1%, (5) 1% to less than 5%, (6) 5% to less than 10%, (7) 10% to less than 20%, (8) 20% to less than 50%, (9) 50% or higher.

We ask participants about their background demographic and socio-economic characteristics, including age, gender, place of residence, education level, marital status, health condition (whether they have chronic diseases), and the primary source of media (television, newspaper, internet, SNS, or others). We also ask about their COVID-19-related experiences, including vaccination status, the number of past infections, and whether they have any acquaintances who died from the virus.
Experimental Design Details
Randomization Method
By computer
Randomization Unit
10,000
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
10,000 individuals
Sample size: planned number of observations
10,000 individuals
Sample size (or number of clusters) by treatment arms
2,500 for each treatment group (one control group and three treatment groups)
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
Given this sample size, we perform a power analysis to compute the minimum detectable effect using a two-sample t-test and assuming equal and unknown standard deviations. At a significance level of alpha = 0.05 and a power (1-beta) = 0.8, the minimum detectable effect is 0.0793 standard deviations. This means that with 2,500 respondents per group, there is an 80\% power to detect an effect size as small as 0.0793 standard deviations between a pair of groups. When increasing the power to 0.9, the minimum detectable effect is 0.0917 standard deviations. Because a minimum detectable effect of less than 0.2 standard deviations is widely accepted in the literature, the power analysis suggests that our sample size is sufficiently large to produce reliable treatment-effect estimates.
IRB

Institutional Review Boards (IRBs)

IRB Name
Ethics Review Board at the University of Tokyo
IRB Approval Date
2023-04-27
IRB Approval Number
23-32
Analysis Plan

There is information in this trial unavailable to the public. Use the button below to request access.

Request Information

Post-Trial

Post Trial Information

Study Withdrawal

There is information in this trial unavailable to the public. Use the button below to request access.

Request Information

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