- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04728594
Emails Promoting COVID-19 Vaccination Among Healthcare Workers
Evaluation of an Email Intervention Promoting COVID-19 Vaccination Among Healthcare Workers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The researchers aim to evaluate the effectiveness of email reminders in promoting COVID-19 vaccinations among Geisinger employees. The project will compare two emails, which will vary in the subject line and email content. Both emails will test different approaches that draw from principles in behavioral science: social proof, reframing, and scarcity. Employees receiving these emails will be compared with employees in a delayed-contact group, who will not receive emails. Employees in the control group will later receive one of the emails.The responses to the emails will help determine the communications later sent to the control group.
All emails will ask recipients if they want to receive a COVID-19 vaccination. If they click on a hyperlink indicating yes, they will be forwarded to an online registration and scheduling homepage. If they click on a hyperlink indicating no, they will be forwarded to an online questionnaire surveying people about their main reason for declining the vaccine at this time. The questionnaire will automatically present information intended to assuage the specific concern that people endorse, followed by a hyperlink to the scheduling site.
The data will be analyzed with logistic regression models with the control group as the reference group, to compare the two email conditions versus the control group. This set of analyses will only be conducted for scheduling a vaccination appointment as opposed to email engagement outcomes (e.g., number of emails opened), which will not be applicable for the control group. A second set of logistic regression models predicting scheduling a vaccination appointment and email engagement will also be run, comparing the two email conditions against each other. The data will be examined two days later (to help decide which email to send to the delayed-control group) and four days later (when the policy for employee vaccination will change, making the content of the email irrelevant).
Update: The researchers looked at 3 days of data - as the emails to the delayed contact group were only sent at that time - and 4 days of data when the policy for employee vaccinations changed.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Danville, Pennsylvania, United States, 17822
- Geisinger
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Employees at Geisinger Health System who have not gotten a COVID-19 vaccination
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Delayed Contact
This group will not receive an email for at least two days.
|
|
Experimental: Social Proof
This group will receive an email that points out that vaccine availability for employees will soon be limited.
It also emphasizes how many fellow health care workers have been vaccinated.
Seeing the behaviors of other people might encourage recipients to copy that behavior.
|
Email
Email
|
Experimental: Reframing Side Effects and Adverse Reactions
This group will receive an email that points out that vaccine availability for employees will soon be limited.
It also addresses concerns about the side effects and adverse reactions of the vaccine.
Due to potentially overblown concerns about the vaccine caused by the salience of side effects in the (social) media, the email attempts to reframe the risks by explicitly noting the small possibility of being affected by serious side effects and by contrasting that to the more severe effects of COVID-19.
As a result of this reframing, recipients might recalibrate their perception of risks and benefits and opt for vaccination.
|
Email
Email
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Employees Who Scheduled Vaccination Appointments After 3 Days
Time Frame: 3 days
|
Binary variable of a scheduled vaccination appointment 3 days after the emails were sent
|
3 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Employees Who Opened Emails After 3 Days
Time Frame: 3 days
|
Binary variable indicating whether the employee opened the email 3 days after the emails were sent
|
3 days
|
Number of Employees Who Clicked Scheduling Links After 3 Days
Time Frame: 3 days
|
Binary variable indicating whether the employee clicked the link to schedule a vaccination appointment 3 days after the emails were sent
|
3 days
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Employees Who Scheduled Vaccination Appointments Until Policy Change (4 Days)
Time Frame: 4 days
|
Binary variable of a scheduled vaccination appointment up to the end of January 19, when new distribution policies were enacted.
|
4 days
|
Number of Employees Who Opened Emails Until Policy Change (4 Days)
Time Frame: 4 days
|
Binary variable indicating whether the employee opened the email up to the end of January 19, when new distribution policies were enacted.
|
4 days
|
Number of Employees Who Clicked the Scheduling Link Until Policy Change (4 Days)
Time Frame: 4 days
|
Binary variable indicating whether the employee clicked the link to schedule a vaccination appointment up to the end of January 19, when new distribution policies were enacted.
|
4 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Michelle M Meyer, PhD, Geisinger Clinic
Publications and helpful links
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
Other Study ID Numbers
- 2021-0128
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ANALYTIC_CODE
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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