跳至主要内容
临床试验/NCT05621226
NCT05621226已完成不适用

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

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 520,000 人开始时间: 2022年11月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
520,000
试验地点
2
主要终点
Patient uptake of COVID bivalent booster

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
Double (Care Provider, Outcomes Assessor)

盲法说明

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.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 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.

结局指标

主要结局

Patient uptake of COVID bivalent booster

时间窗: During the 30 days after receiving the SMS/MMS intervention

Whether patients receive a bivalent COVID booster at the pharmacy in question

次要结局

  • Patient uptake of COVID bivalent booster(90 days after receiving the SMS/MMS intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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