Rapid Turnaround, Home-based Saliva Testing for COVID-19

Trial ID or NCT#

NCT04568122

Status

not recruiting iconNOT RECRUITING

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

Ages Eligible for Study: Older than 2 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: Yes
Inclusion Criteria:
  1. - 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
Exclusion Criteria:
  1. - 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)

Manu Prakash
Euan A. Ashley
Euan A. Ashley
Cardiologist, Heart failure cardiologist
Associate Dean, School of Medicine, Roger and Joelle Burnell Professor of Genomics and Precision Health, Professor of Medicine (Cardiovascular Medicine), of Genetics, of Biomedical Data Science and, by courtesy, of Pathology

Contact us to find out if this trial is right for you.

Contact

Study Team
650-374-0085