Rapid Turnaround, Home-based Saliva Testing for COVID-19
Trial ID or NCT#
Status
Purpose
The aim of the study is to demonstrate the feasibility and validity of a saliva based home surveillance monitoring test for SARS-CoV-2 infection. Participants will be asked to carry out as many tests as are included in the bag they are provided, on a daily basis until they are used up.
Official Title
Rapid Turnaround, Home-based Saliva Testing for COVID-19
Eligibility Criteria
- * Hospitalized patients
- * Hospitalized at ÌÇÐÄ´«Ã½ for COVID-related complications and tested positive for SARS-CoV-2 with a PCR-based test * Able to understand and consent to study and with a clinical trajectory likely to be consistent with multi-day participation* High-risk/positive population
- * Seeking testing for suspected COVID or a participant in a study of COVID-positive outpatients * Own an internet-enabled phone or device capable of loading web pages, receiving text messages, and taking/uploading photos. * Willing to participate in the study for 6 months* Low-risk population
- * Own an internet-enabled phone or device capable of loading web pages, receiving text messages, and taking/uploading photos. * Willing to participate in the study for 6 months
- * All participants:
- * Participants with salivary gland dysfunction (including patients with Sjogren's disease or those with xerostomia associated with lupus or rheumatoid arthritis) * Participants will not be eligible if they identify any reason they are unable to participate in the study* High-risk/positive population
- * Participants who have color blindness * Participants unable to operate the SnapDx device* Low-risk population
- * Participants with prior confirmed SARS-CoV-2 infection * Participants who have color blindness * Participants unable to operate the SnapDx device
Investigator(s)
Contact us to find out if this trial is right for you.
Contact
Study Team
650-374-0085
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