- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05182554
COVID-19 Messaging for Vaccination
Increasing the Effectiveness and Diffusion of COVID-19 Messaging for Vaccination
Study Overview
Status
Conditions
Detailed Description
The study will have three treatment arms and a control group. Each of the treatments will be randomized at the county level and will be initiated through a Facebook ad campaign.
Experimental Sample: The experimental sample includes all states where less than 60% of the total population had received a first dose of Covid-19 vaccine by October 21, 2021. There are 1402 counties in the 19 states satisfying those criteria (Alabama, Alaska, Arkansas, Georgia, Idaho, Iowa, Indiana, Louisiana, Michigan, Mississippi, Missouri, Montana, North Dakota, Ohio, Oklahoma, South Carolina, Tennessee, West Virginia, Wyoming). Excluding the five counties with missing data, there are 1,397 counties in the experiment, of which there are 468 counties in the control group, 310 counties in T1 ("direct" messaging) treatment, 309 counties in T2 ("friends" messaging), and 310 counties in T3 ("gossips" messaging).
The following procedures will be used:
- Treatment Group 1 ("Direct" messaging): The investigators will conduct a Facebook ad campaign to show content about COVID-19 vaccination to a large number of Facebook users. Facebook will allocate ad credits across users in treatment areas. The ads will be displayed twice per week for 3-4 weeks. Like for any Facebook ad, individuals can choose to whether or not to watch the video and can close the ad at any time. If individuals wish, they can also share any of the content with others. The videos shown in the ads will be hosted on our project Facebook page "Doctors for Coronavirus Prevention." As in previous projects by the investigators, a health professional (normally wearing a white coat or scrubs) will read very short scripts directly onto the camera (see eg. https://www.facebook.com/doctors4covidprevention/posts/104965558099200 for an example).
- Treatment Group 2 ("Friends" messaging): For this group, the Facebook ad campaign will recruit individuals to become "vaccine ambassadors" to help spread the word about vaccination to their friends, families and communities. Recruitment ads will be disseminated in a similar manner to the content in T1. Individuals will be able to share the ad with others. Individuals interested in learning more can click through a link in the ad to the vaccine ambassador webpage. Participants can consume or share any of the information on the webpage. Interested individuals can also enroll formally as vaccine ambassadors. They can share their contact information with the study to a) be entered into prize lotteries, b) receive reminders to share content with others, c) be contacted in the future for possible follow-up surveys. They will be asked to give their informed consent at this time and will be screened based on whether they live in a treated county and whether they are 18 years or older.
- Treatment Group 3 ("Gossips" messaging): This treatment looks the same as Treatment Group 2, except the recruitment ads will differ slightly. If the individual clicks through to learn more about vaccine ambassadors, they will also be reminded to share the invitation with people they know who are often the source of important news or information.
- Control: individuals in these counties will receive no intervention and will never be contacted by members of the study team.
Treatment and control status at the county level will be merged with aggregated and de-identified datasets to measure COVID vaccinations, COVID symptoms, and cases, and engagement with the vaccine ambassador content.
The study team will create a series of websites with materials that the vaccine ambassadors can share with friends, family and others in their communities. This same content will be disseminated through sponsored Facebook ads in T1. On the website, the framing of the vaccine-related videos with either a "fact" or "myth" frame will be randomized. The purpose is to study which framing is more effective at engaging users.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Massachusetts
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Cambridge, Massachusetts, United States, 02139
- Massachusetts Institute of Technology
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Facebook user
- Over 18 years old
- In a geographic area targeted by the study
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
No intervention in this arm; the study team will examine publicly available county- and zip code-level outcomes in this group.
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Experimental: Treatment 1: Direct
Facebook users in the area receive ads which include videos of health professionals telling them to get vaccinated.
The health professionals answer common questions about Covid-19 vaccines (e.g. are they safe / are they free).
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Receive ads on Facebook or through our website with videos in which health professionals tell people to get the Covid-19 vaccine.
The health professionals answer common questions about the Covid-19 vaccine, such as how mRNA vaccines work, and what types of side effects to expect.
|
|
Experimental: Treatment 2: Friends
Facebook users in the area receive ads which include videos of health professionals encouraging them to help their friends to get vaccinated.
There is also a link in the ad to a website build by the study team.
This website hosts videos which answer common questions about vaccination (the same videos which are directly served to Facebook users in Treatment 1).
|
Receive ads on Facebook or through our website with videos in which health professionals tell people to get the Covid-19 vaccine.
The health professionals answer common questions about the Covid-19 vaccine, such as how mRNA vaccines work, and what types of side effects to expect.
Receive ads on Facebook with videos in which health professionals tell people to encourage their unvaccinated friends to get the Covid-19 vaccine.
Adults in participating geographic areas can sign up to be a "vaccine ambassador" on a website that the study team has built.
The study team will send updates to vaccine ambassadors when new content has been posted to the website (e.g. a new video) and/or to remind the vaccine ambassadors to encourage their friends to get vaccinated.
The study team will incentivize vaccine ambassadors by entering participating ambassadors into a lottery for a prize.
The same videos will be displayed using two different frames: a "myth" frame and a "fact" frame.
Visitors to the vaccine content website will randomly receive one framing of each video.
The order in which videos appear on the vaccine content website will be randomized.
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Experimental: Treatment 3: Gossips
Facebook users in the area receive ads which include videos of health professionals encouraging them to nominate their most influential friends to help their friends get vaccinated.
The difference from Treatment 2 is that the health professionals call on Facebook users to get their most influential friends to do the convincing about the vaccine.
There is also a link in the ad to a website built by the study team.
This website hosts videos which answer common questions about vaccination (the same videos that are directly served to Facebook users in Treatment 1).
|
Receive ads on Facebook or through our website with videos in which health professionals tell people to get the Covid-19 vaccine.
The health professionals answer common questions about the Covid-19 vaccine, such as how mRNA vaccines work, and what types of side effects to expect.
Adults in participating geographic areas can sign up to be a "vaccine ambassador" on a website that the study team has built.
The study team will send updates to vaccine ambassadors when new content has been posted to the website (e.g. a new video) and/or to remind the vaccine ambassadors to encourage their friends to get vaccinated.
The study team will incentivize vaccine ambassadors by entering participating ambassadors into a lottery for a prize.
The same videos will be displayed using two different frames: a "myth" frame and a "fact" frame.
Visitors to the vaccine content website will randomly receive one framing of each video.
The order in which videos appear on the vaccine content website will be randomized.
Receive ads on Facebook with videos in which health professionals tell people to get their most influential friends to encourage their unvaccinated friends to get the Covid-19 vaccine.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in County-Level Covid-19 Vaccination Measured by Inverse Hyperbolic Sine
Time Frame: During intervention (6 weeks) and after intervention (3 weeks)
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County-level Covid-19 vaccination rates were analysed using publicly available data.
The number of new vaccinations in each county was transformed using the inverse hyperbolic sine because the underlying vaccination count data were right-skewed and included zeros.
Larger numbers are considered better in the context of the study (more people vaccinated).
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During intervention (6 weeks) and after intervention (3 weeks)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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COVID-19 cases
Time Frame: During intervention and up to 6 months after intervention
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Measured by publicly available county- or zip code-level Covid-19 cases, in some areas also split by vaccinated vs unvaccinated status.
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During intervention and up to 6 months after intervention
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COVID-19 symptoms prevalence
Time Frame: During intervention and up to 6 months after intervention
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Measured by publicly available county- or zip code-level Covid-19 symptoms, in some areas also split by vaccinated vs unvaccinated status.
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During intervention and up to 6 months after intervention
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COVID-19 hospitalization and mortality
Time Frame: During intervention and up to 6 months after intervention
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Measured by data on patients admitted to hospitals or who have been recorded to have died from Covid-19, , in some areas also split by vaccinated vs unvaccinated status.
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During intervention and up to 6 months after intervention
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Vaccine hesitancy
Time Frame: During intervention and up to 6 months after intervention
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Measured by publicly available county- or zip code-level surveys
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During intervention and up to 6 months after intervention
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Movement and Travel
Time Frame: During intervention and up to 6 months after intervention
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Measured using mobile phone location data of Facebook users.
Vaccinated people may be more likely to take risks, including travel.
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During intervention and up to 6 months after intervention
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School closures
Time Frame: During intervention and up to 6 months after intervention
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Increased cases could lead to more school closures.
The investigators do not expect the study to be well-powered on this outcome.
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During intervention and up to 6 months after intervention
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Number of vaccine ambassador volunteers
Time Frame: During intervention
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This will be compared between the "friends" and "gossips" treatment groups.
This will include people who start to sign up to be vaccine ambassadors as well people who complete the vaccine ambassador consent process.
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During intervention
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Esther Duflo, PhD, Massachusetts Institute of Technology
- Principal Investigator: Ben Olken, PhD, Massachusetts Institute of Technology
- Principal Investigator: Abhijit Banerjee, PhD, Massachusetts Institute of Technology
- Principal Investigator: Marcella Alsan, MD, PhD, Harvard Kennedy School
- Principal Investigator: Arun Chandrasekhar, PhD, Stanford University
- Principal Investigator: Emily Breza, PhD, Harvard University
- Principal Investigator: Paul Goldsmith-Pinkham, PhD, Yale University
- Principal Investigator: Emily Hoppe, PhD Student, Johns Hopkins School of Nursing
- Principal Investigator: Pierre-Luc Vautrey, PhD Student, Massachusetts Institute of Technology
- Principal Investigator: Lisa Ho, PhD Student, Massachusetts Institute of Technology
- Principal Investigator: Lucy Ogbu-Nwobodo, MD, MGH/McLean Harvard Psychiatry Program
- Principal Investigator: Erica Warner, ScD, MPH, Harvard Medical School & Massachusetts General Hospital
- Principal Investigator: Carlos Torres, MD, Massachusetts General Hospital
- Principal Investigator: Fatima Stanford, MD, MPH, MPA, Harvard Medical School & Massachusetts General Hospital
- Principal Investigator: Sarah Eichmeyer, PhD, Ludwig-Maximilians - University of Munich
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2106000397
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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