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临床试验/NCT05612360
NCT05612360已完成不适用

Message Encouraging Vaccination in Preparation for the Holidays

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
COVID bivalent booster receipt

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. Ther focal comparison in this experiment is between a message encouraging vaccination by reminding participants that the holiday season is just a few weeks away and getting vaccinated will allow them to more safely gather with loved ones and a control message telling patients that an updated COVID booster vaccine is waiting for them. The intervention testing if text messages encouraging vaccination by reminding participants that the holiday season is just a few weeks away and getting vaccinated will allow them to more safely gather with loved ones will produce more vaccinations than otherwise identical messages.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

COVID bivalent booster receipt

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

  • COVID bivalent booster receipt(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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