COVID-19 Bivalent Booster Megastudy
1 other identifier
interventional
2,600,000
1 country
1
Brief Summary
This megastudy is a massive randomized controlled trial. By randomizing participants to 10 different intervention conditions simultaneously, the investigators will be able to compare the effectiveness of different interventions to one another and to a control group (in which individuals will only receive the usual communications from their partner organization) to identify which interventions significantly increase vaccination rates. Pharmacy customers will be randomly assigned to receive one of the interventions designed by team scientists to encourage vaccination or to a control group. The baseline intervention will be based on the top-performing SMS intervention identified in the investigators previous megastudies on encouraging vaccination (Milkman et al., 2021b, 2022). Pharmacy customers will receive SMS messages conveying that a COVID booster vaccine is reserved or waiting for them at the pharmacy. Additional behavioral science messaging strategies will be tested by building off of this baseline intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable covid19
Started Nov 2022
Shorter than P25 for not_applicable covid19
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 3, 2022
CompletedStudy Start
First participant enrolled
November 3, 2022
CompletedFirst Posted
Study publicly available on registry
November 7, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 8, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
February 6, 2023
CompletedMarch 3, 2023
March 1, 2023
1 month
November 3, 2022
March 1, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Patient uptake of the COVID bivalent booster
Whether patients receive a bivalent COVID booster at the pharmacy in question
During the 30 days after receiving the SMS/MMS intervention
Secondary Outcomes (2)
Patient uptake of the COVID bivalent booster
60 days after receiving the SMS/MMS intervention
Patient uptake of the COVID bivalent booster
90 days after receiving the SMS/MMS intervention
Study Arms (11)
Holdout control condition with no message
NO INTERVENTIONParticipants will only receive the standard pharmacy messaging.
Control condition with "waiting for you" message
EXPERIMENTALThis control condition will use the text message that we've found to be the best performing in our last mega-study of vaccine text messages to recommend a COVID vaccination.
Control condition with "waiting for you" message with a GIF
EXPERIMENTALThis control condition will use the text message that we've found to be the best performing in our last mega-study of vaccine text messages and includes a GIF to recommend a COVID vaccination.
Planning message recommending same time/location as last vaccination
EXPERIMENTALThis condition will use a text message recommending the same time and location as the participant's last vaccination to get a COVID vaccination.
Message from local pharmacy team
EXPERIMENTALThis condition will use a text message from the participant's local pharmacist recommending a COVID vaccination.
Message including link to resources combating misinformation
EXPERIMENTALThis condition will use a text message including a link to to resources combating misinformation and then recommend a COVID vaccination.
Message including link to resources combating misinformation with a GIF
EXPERIMENTALThis condition will use a text message including a link to to resources combating misinformation and then recommend a COVID vaccination and will include a GIF.
Message offering free round trip ride to the pharmacy
EXPERIMENTALThis condition will use a text message offering a free round trip ride to the pharmacy to get a COVID vaccination.
Message communicating latest data on COVID transmission in patient's area
EXPERIMENTALThis condition will use a text message informing the participant of the latest data on COVID transmission in participant's area and recommend a COVID vaccination.
Message encouraging vaccination in preparation for the holidays
EXPERIMENTALThis condition will use a text message to encourage a COVID vaccination in preparation for the holidays.
Message conveying the CDC recommends vaccination
EXPERIMENTALThis condition will use a text message to encourage a COVID vaccination by conveying the CDC recommends vaccination.
Interventions
Participants will receive text messages per descriptions listed in the arms.
Eligibility Criteria
You may qualify if:
- Patient of a large retail pharmacy that has opted into receving SMS messages from the pharmacy and has received their primary COVID vaccination series.
You may not qualify if:
- The patient unsubscribed from texts before the send date and time of the patient's SMS/MMS message
- The patient received a bivalent COVID booster before the send date and time of the patient's SMS/MMS message.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- CARE PROVIDER, OUTCOMES ASSESSOR
- Masking Details
- As treated participants will receive text messages, there is no scope for blinding. Care providers will not be made aware of subjects' participation in the study, or assigned treatment arms. The study team will only receive data on subjects' assigned arms and outcomes at the end of the study.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 3, 2022
First Posted
November 7, 2022
Study Start
November 3, 2022
Primary Completion
December 8, 2022
Study Completion
February 6, 2023
Last Updated
March 3, 2023
Record last verified: 2023-03
Data Sharing
- IPD Sharing
- Will not share