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 Stanford Health Care 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
View on ClinicalTrials.gov