The formats of epidemiological risk information disclosure and citizens’ voluntary self-reporting for close contact: report accuracy, time consumption, and privacy concerns

Last registered on October 17, 2022

Pre-Trial

Trial Information

General Information

Title
The formats of epidemiological risk information disclosure and citizens’ voluntary self-reporting for close contact: report accuracy, time consumption, and privacy concerns
RCT ID
AEARCTR-0010036
Initial registration date
September 09, 2022

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
October 17, 2022, 10:54 AM EDT

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

Locations

Region

Primary Investigator

Affiliation
School of Economics and Management, Beihang University, China

Other Primary Investigator(s)

PI Affiliation
Beihang University

Additional Trial Information

Status
Completed
Start date
2022-08-08
End date
2022-09-20
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
Timely contact tracing is important to prevent the occurrence and control the spread of an infectious disease. To complement the active case investigation and contact tracing, one often adopted practice is to publish lists of times and locations of risk and ask citizens to engage in self-reporting in case they find that they have visited the listed places in the corresponding time windows. This study tries to provide the first experimental study on how different formats to display the times and locations of risk affect the accuracy of self-reporting. Our task for the subjects is to read a list of times and locations of risk within a three-day window and compare the list with their own route of visits to decide whether to report being a close-contact or not. We construct the hypothetical lists and routes of visits of the subjects using published lists in the past, varying the length of the list, the routes of visits, and whether there is an overlap between the two for across tasks. The baseline treatment of display format is to sort places and times of risk by individuals with positive nucleic acid test. We compare subjects’ self-report accuracy with two alternative formats: sorting the information by locations, and by time, eliminating link between individuals and the places of risk. We hypothesize that the accuracy in the two alternative formats, in which information is organized in an easier way for search, is higher than the baseline treatment. We will also measure individuals’ privacy concerns regarding the list of risk information and expect the alternative formats to lead to lower concerns of privacy. Another dependent variable to consider is the time spent for the task.
External Link(s)

Registration Citation

Citation
Liu, Ning and Qiying Wu. 2022. "The formats of epidemiological risk information disclosure and citizens’ voluntary self-reporting for close contact: report accuracy, time consumption, and privacy concerns." AEA RCT Registry. October 17. https://doi.org/10.1257/rct.10036-1.0
Experimental Details

Interventions

Intervention(s)
We have three between-subject treatment groups, receiving lists of times and locations of risk in three formats, where the information is clustered 1) by the individuals who have positive nucleic acid test results and travelled to these places, 2) by the dates of the time of risk, or 3) by the locations of risk.
Intervention Start Date
2022-08-08
Intervention End Date
2022-09-20

Primary Outcomes

Primary Outcomes (end points)
Accuracy of the self-report, response time, and perceived privacy concerns.
Primary Outcomes (explanation)
1. Accuracy of the self-report.
Accuracy of each task is 1 if the subject chooses to self-report (not to self-report) an overlap with the list of risk when there is at least one overlap (is no overlap) between individual route of visits and the list of risk.
2. Response time
We will analyze the response time to accomplish each task, from seeing the information page until submitting the self-report decision.
3. Perceived privacy concerns
We measure subjects’ privacy concerns regarding track disclosure using three questions with 7 Likert scales (ranging from 1, strongly disagree, to 7, strongly agree). The questions are adapted from the items for perceived privacy concern in Esmaeilzadeh et al. (2020) and the items of improper access in the measure of Internet Privacy Concern in Hong and Thong (2013).
We will use the sum of the three items as the subjects’ concern, higher means having more concerns.
What we show in the experiment is (with English translation in brackets):
(1) 我认为以上情境中的风险点通报方式泄露了过多个人信息。[Regarding the way to report risky locations in scenarios above, I am concerned about the privacy of my personal information.]
(2) 针对以上情境中的风险点通报方式,我担心个人隐私泄露。[Regarding the way to report risky locations in scenarios above, I am concerned that my personal information will be used for unintended purposes.]
(3) 针对以上情境中的风险点通报方式,我担心我的个人信息会被滥用。[Regarding the way to report risky locations in scenarios above, I think that the publishers could take more steps to prevent better the misuse of my personal information.]

Secondary Outcomes

Secondary Outcomes (end points)
Opinion regarding the information provider
Secondary Outcomes (explanation)
We have another question in the same format as the privacy concern questions to measure subjects’ opinion regarding the information provider.
针对以上情境中的风险点通报方式,我认为信息发布者可以进一步改良通报方式以防止我的个人信息被滥用。[Regarding the way to report risky locations in scenarios above, I think that the publishers could take more steps to prevent better the misuse of my personal information.]

Self-report support, measuring their support by providing truthful information.
考虑到我的行程信息会通过以上情境中的风险点通报方式呈现,我对信息上报态度是(1表示“有所保留”,7表示“完全如实”)是 [considering that my own travel information may be presented in the way I saw as in the list of times and locations of risk, my attitude towards self-reporting is (1-with reservation, 7-completely truthfully).]

请问过去的30天里您进行了几次核酸检测?[How many nucleic acid tests have you gone through during the past 30 days?]

Experimental Design

Experimental Design
Our task for the subjects is to read a list of times and locations of risk within a three-day window and compare the list with their own route of visits to decide whether to report being a close-contact or not. We construct the hypothetical lists and routes of visits of the subjects using published lists in the past, varying the length of the list, the routes of visits, and whether there is an overlap between the two for across tasks. The baseline treatment of display format is to sort places and times of risk by individuals with positive nucleic acid test. We compare subjects’ self-report accuracy with two alternative formats: sorting the information by locations, and by time, eliminating link between individuals and the places of risk.
Experimental Design Details
We randomly assign our participants into three groups that showing the lists of risk in different formats. We have three experimental groups, receiving places and times of risk listed in three different formats, with examples of the formats given in the "Intervention (Hidden)" section above.

In the control treatment (labeled as the "by-case treatment"), the information is sorted by the individuals confirmed with a positive nucleic acid test result. In the two treatment groups, information regarding the individual cases is excluded.

In one treatment group (labeled as the "by-time treatment"), the information is sorted by the time, followed by the places overlapped with trace routes of individuals with positive nucleic acid test results.

In the other treatment group (labeled as the "by-place treatment"), the information is sorted by the places, followed by the time span overlapped with trace routes of individuals with positive nucleic acid test results.

Each participant will answer six tasks, each with a different (hypothetical) personal flow track and a list of places in risk. Their task is to compare if there is any overlap in time and location between the two pieces of information.
In addition to the main tasks, we also collect their privacy concerns regarding the treatment-specific information provision format, opinion of the information provider, the number of NATs received, and demographic information of their place of living, gender, age, education, marital status.
Randomization Method
Randomization will be done through dingwei.netease survey platform inbuilt randomization feature.
Randomization Unit
Individual
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
N/A
Sample size: planned number of observations
1050 individuals, each answering 6 questions, in which the subjects will compare the given (hypothetical) three-day route track with a list of times and locations of epidemiological risk.
Sample size (or number of clusters) by treatment arms
about 350 individuals in each treatment
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
We chose the minimum detectable effect size for accuracy rate to be 4%, and conducted power test using a pilot study. Power test according to linear probability model with sd=0.46, 6 observations per subject, power=0.8, N>346 Power test according to binomial model with p1=0.7, p2=0.74, 6 observations per subject, power=0.8, N>329
IRB

Institutional Review Boards (IRBs)

IRB Name
Institutional Review Board of the School of Economics and Management, Beihang University
IRB Approval Date
2022-07-20
IRB Approval Number
N/A
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