- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05080179
Impact of Nudges on Downloads of COVID-19 Exposure Notification Smartphone Apps: A Randomized Trial
The Interactive Effect of Social Norm and Self (vs. Others) Benefit Nudges on Downloads of COVID-19 Exposure Notification Smartphone Apps: A Randomized Trial
Eligible participants who were active beneficiaries of a large insurer living in Pennsylvania were sent an email encouraging them to download the contact tracing app in Pennsylvania, COVID Alert PA.
Participants will be randomly assigned to one of four conditions in a 2 (Self-benefit vs. Other-Benefit) x 2 (Social Norms Present vs. Social Norms absent) design.
All participants received an email that said :
"COVID Alert PA is the official Exposure Notification App from the Pennsylvania Department of Health. Join Penn Medicine in the fight against COVID-19 and download COVID Alert PA today!"
---Investigators manipulated the content here---
"The app uses Bluetooth to sense when one person is in close contact with another person with the app. If someone tests positive for COVID-19, and they decide to upload the information to the health department, people who have the app and who have been in contact with them will be alerted.
If you are interested in downloading the app, please click COVID Alert PA. We appreciate you joining our efforts. Together we can beat COVID-19!"
In the Other-Benefit condition, it said: "It can help you reduce your risk of unknowingly spreading the virus to your friends, family, and larger community."
In the Self-Benefit condition, it said: "It can help you determine where and when to get testing, and how to get care if you need it."
In the Social Norms Present condition, it said: "Over 650,000 Pennsylvanians have already downloaded the app!"
In the Social Norms Absent condition, it said the statement about social norms above.
Participants who do not open the initial email received a follow-up email.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
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Philadelphia, Pennsylvania, United States, 19146
- Independence Blue Cross (IBX)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Eligible participants were active beneficiaries of a large insurer living in Pennsylvania.
Exclusion Criteria:
- Participants who did not subscribe to offers and promotions emails were excluded, as were Medigap beneficiaries.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Self-Benefit/Social Norm
As part of their email, they read, "It can help you determine where and when to get testing, and how to get care if you need it."
and "Over 650,000 Pennsylvanians have already downloaded the app!"
|
As part of their email, they will read, "It can help you determine where and when to get testing, and how to get care if you need it."
and "Over 650,000 Pennsylvanians have already downloaded the app!"
|
Experimental: Self-Benefit/No Social Norm
As part of their email, they read, "It can help you determine where and when to get testing, and how to get care if you need it."
They did not read any information about the number of Pennsylvanians who downloaded the app.
|
As part of their email, they will read, "It can help you determine where and when to get testing, and how to get care if you need it."
They will not read any information about the number of Pennsylvanians who downloaded the app.
|
Experimental: Other Benefit/Social Norm
As part of their email, they read, "It can help you reduce your risk of unknowingly spreading the virus to your friends, family, and larger community."
and "Over 650,000 Pennsylvanians have already downloaded the app!"
|
As part of their email, they will read, "It can help you reduce your risk of unknowingly spreading the virus to your friends, family, and larger community."
and "Over 650,000 Pennsylvanians have already downloaded the app!"
|
Experimental: Other Benefit/No Social Norm
As part of their email, they read, "It can help you reduce your risk of unknowingly spreading the virus to your friends, family, and larger community."
They did not read any information about the number of Pennsylvanians who downloaded the app.
|
As part of their email, they will read, "It can help you reduce your risk of unknowingly spreading the virus to your friends, family, and larger community."
They will not read any information about the number of Pennsylvanians who downloaded the app.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Click on Link to Download COVID Alert PA App
Time Frame: 48 days
|
The investigators measured choice to click on the link to download the COVID Alert PA app or not, conditional on opening the email.
Because participants may not immediately open their e-mail, or may return to the e-mail to click the link, we allowed for a period of approximately 7 weeks or 48 days from date of initial e-mail for completion of outcome measure.
|
48 days
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 844564
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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