About this trial
Last updated 3 years ago
Study ID
AB-001-01
Status
Completed
Type
Interventional
Phase
N/A
Placebo
No
Accepting
2+ Years
All
Trial Timing
Ended 3 years ago
What is this trial about?
The objective of the study is to determine the usability of the GlowTest COVID-19 Antigen
Home Test in a simulated home use environment. This is an open label study to evaluate the
usability of the GlowTest COVID-19 Antigen Home Test using information from the Quick
Reference Instructions and website.
What are the participation requirements?
Inclusion Criteria
- An Institutional Review Board (IRB) approved informed consent/assent is signed and dated prior to any study-related activities.
- Males and females ages 2 and older.
- Subject is willing to provide a self-collected nasal swab sample. (If under the age of 14, the sample will be collected by an adult.)
- Subject agrees to complete all aspects of the study
Exclusion Criteria
- Subject has a visual impairment that cannot be restored with glasses or contact lenses.
- Subject has prior medical or laboratory training.
- Subject uses home diagnostics, e.g., glucose meters, HIV tests.
- Subject has prior experience with home COVID test kits.