It started with a simple email.
When the novel coronavirus known as COVID-19 was raging across America last April, NBA officials were frantically searching for an easy and affordable way to test players, get timely results and save the 2020 basketball season.
About the same time, Anne Wyllie, an associate research scientist in Epidemiology (Microbial Diseases) at the Yale School of Public Health, published preliminary research showing that for the diagnosis of COVID-19, saliva was as sensitive and reliable as the intrusive nasopharyngeal swabs that were being widely used and were considered the testing gold standard.
Robby Sikka, vice president of basketball performance and technology for the NBA’s Minnesota Timberwolves, spotted Wyllie’s paper and, eager to know more, emailed her and her colleague Assistant Professor Nathan Grubaugh, who had come together to help lead the testing of samples for Yale’s IMPACT biorepository.
The contact was fortuitous.
Wyllie and Grubaugh were already developing a more efficient and importantly, cost-effective saliva-based test, which they would later call SalivaDirect™. What they lacked was a pool of research participants to assess the new protocol’s efficacy for testing asymptomatic individuals. And now, the NBA was knocking on their door.
After a flury of emails and Zoom meetings, Wyllie, Grubaugh, and the NBA, with important buy-in from the NBA Players’ Association, launched a study called SWISH (Surveillance With Improved Screening and Health) to further evaluate the efficacy of the SalivaDirect™ protocol. Up to 500 NBA players and staff were enrolled in the study to see if SalivaDirect™ could serve as a reliable surveillance measure for COVID-19.