SARS-CoV-2 Acute Respiratory Disease
Conditions
Brief summary
The primary objective of this study is to identify and describe patient behaviors and clinical outcomes among patients who have tested positive for mild to moderate COVID-19.
Detailed description
This virtual observational cohort study will describe patient behaviors and clinical outcomes of subjects who tested positive for COVID-19. Among those with positive tests, predictors of time to recovery, post-COVID function and outcomes will be identified. Individuals who test negative and positive for SARS-CoV-2 will be enrolled in the study.
Interventions
OTHERSARS-CoV-2 Positive
Participants who have tested positive for SARS-CoV-2, both with and without symptoms
OTHERSARS-CoV-2 Negative
Participants who have tested negative for SARS-CoV-2
Sponsors
Everly Health
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Age \>=18 years * Individuals with a valid diagnostic COVID-19 test result
Exclusion criteria
\- Unable or unwilling to provide informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To identify and describe patient behaviors and clinical outcomes among patients who have tested positive for COVID-19 | Up to 12 months |
Secondary
| Measure | Time frame |
|---|---|
| To describe recovery in patients with test-confirmed COVID-19 infection including time to recovery and functional improvement | Up to 12 months |
| To develop prediction tools for time to recovery, function and outcomes in patients with COVID-19 identified by home testing | Up to 12 months |
| To describe users and the utilization of COVID-19 home testing over time by geography, demographics, and comorbidity | Up to 12 months |
| To describe the feasibility of COVID-19 home testing | Up to 12 months |
Countries
United States
Outcome results
None listed