SARS-CoV-2
Conditions
Brief summary
This study will investigate antibody levels with respect to time since receiving a COVID-19 booster shot. The study will be decentralized, where participants can complete all study tasks at home. Self-reported participant information will be collected via surveys conducted at intake and monthly throughout the study. Participants will also perform monthly at-home capillary blood draws via YourBio devices that will be mailed to the designated laboratory for sample processing and antibody testing.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Lives in the continental United States. * Has been vaccinated against COVID-19 with a U.S.-authorized vaccine (that is, received the single shot J&J vaccine or both shots in the Pfizer or Moderna series). * Has received a COVID-19 booster between September 2021 and screening. * Is willing and able to submit vaccination card photo(s). * Is willing and able to self-collect capillary blood 3 times during the study period via an at-home whole-blood collection device (that is, the YourBio TAP II Device).
Exclusion criteria
* Has been diagnosed with significant cognitive impairment or dementia. * Has received more than one COVID-19 vaccine booster at screening. * Is currently participating in a COVID-19 vaccine clinical trial. * Is currently receiving chemotherapy or has received chemotherapy in the past 6 months. * Is currently taking steroids, such as prednisone, for any condition. * Has been diagnosed with or is taking medications for rheumatoid arthritis (RA), lupus or multiple sclerosis (MS). * Has received an organ transplant * Is currently undergoing dialysis of any kind (for example, hemodialysis or chronic ambulatory dialysis) for kidney disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Antibody Levels Since Receiving a COVID-19 Booster Vaccine at 0, 1, and 2 Months Post Enrollment | Baseline (Month 0), Month 1, and Month 2 |
Countries
United States