Official Title
Feasibility of Self-monitoring and Patient Decision Support for Suspected COVID-19 Patients After Emergency Department Discharge
Brief Summary

This feasibility study is being conducted to understand how discharged emergency department patients who were tested for the SARS-CoV-2 virus (COVID-19) engage with a symptom-tracking web application. Study participants that are enrolled in the study will be asked to enter daily information about their health into the CovidX web application (app.). In addition, patients will answer questions regarding anxiety levels, use a pulse oximeter to record information (if you own one or are given one). The investigators predict that participants will be able to engage with the CovidX web application over several days to weeks for the purposes of symptom tracking, and may have decreased anxiety over the study period.

Withdrawn
COVID
COVID-19
SARS-CoV 2

Other: Symptoms entered into the CovidX application

Participants are asked to enter symptoms into the CovidX application at least daily for 30 days. Additionally, they will enter demographic information and some survey information will be collected.

Eligibility Criteria

Inclusion Criteria:

- Reported symptoms of viral illness during ED encounter

- Tested for SARS-CoV-2 (COVID-19) during ED encounter

- Discharged home from the Emergency Department

Exclusion Criteria:

- Prisoners

- Residents of congregate living facilities who are already being monitored

- Baseline oxygen requirement

- Patients whose primary goals of care are palliative

- Pregnant women

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A

Kathleen Li, MD, Principal Investigator
University of Michigan

Vironix Health Incorporated
NCT Number
Keywords
Coronavirus
MeSH Terms
COVID-19
Emergencies