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NCT05621226 Clinical Trial

Message Communicating Latest Data on COVID-19 Transmission in Patient's Area

COVID-19 Clinical Trial

Official title:
Message Communicating Latest Data on COVID-19 Transmission in Patient's Area

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05621226
Other study ID # 851911-Trial F
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 3, 2022
Est. completion date February 6, 2023

Study information
Verified date March 2023
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This experiment is part of a megastudy with a total of ten experimental conditions and a holdout control condition to which patients will be randomly assigned. The focal comparison in this experiment is between a message encouraging vaccination by communicating to patients that they live in an area with significant COVID transmission and a control message telling patients that an updated COVID booster vaccine is waiting for them.

Recruitment information / eligibility
Status Completed
Enrollment 520000
Est. completion date February 6, 2023
Est. primary completion date December 8, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Exclusion Criteria: 1. The patient unsubscribed from texts before the send date and time of the patient's SMS/MMS message 2. The patient received a bivalent COVID booster before the send date and time of the patient's SMS/MMS message.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• COVID Booster text messages
Participants will receive text messages per descriptions listed in the arms.

Locations
Country Name City State
United States University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Patient uptake of 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 Patient uptake of COVID bivalent booster Whether patients receive a bivalent COVID booster at the pharmacy in question 60 days after receiving the SMS/MMS intervention
Secondary Patient uptake of COVID bivalent booster Whether patients receive a bivalent COVID booster at the pharmacy in question 90 days after receiving the SMS/MMS intervention
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