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临床试验/NL-OMON23180
NL-OMON23180已完成不适用

Remote Early Detection of SARS-CoV-2 infections

niversitair Medisch Centrum Utrecht (UMCU), Julius Center0 个研究点目标入组 20,000 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Resident of the Netherlands
  • At least 18 years old
  • Informed consent provided (electronic)
  • Willing to adhere to the study procedures described in this protocol
  • Must have a smartphone that runs at least Android 8.0 or iOS 13.0 operating systems and is active for the duration of the study (in the case of a change of mobile number, study team should be notified)
  • Be able to read, understand and write Dutch

排除标准

  • Previous positive SARS-CoV-2 test result (confirmed either through PCR/antigen or antibody tests) (self-reported)
  • Previously received a vaccine developed specifically for COVID-19 or in possession of an appointment for vaccination in the near future
  • Current suspected (e.g. waiting for test result) coronavirus infection or symptoms of a coronavirus infection (self-reported)
  • Participating in any other COVID-19 clinical drug, vaccine, or medical device trial
  • Electronic implanted device (such as a pacemaker)
  • Pregnant at time of informed consent (self-reported)
  • Suffering from cholinergic urticaria (per the Ava bracelet’s User Manual)
  • Staff involved in the management or conduct of this study

研究者

发起方
niversitair Medisch Centrum Utrecht (UMCU), Julius Center

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