Home antibody tests put to the test: can you read your own COVID-19 result?
NCT ID NCT04393961
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Researchers are studying whether people can accurately use a rapid COVID-19 antibody test at home. Participants in New York City who have recovered from or suspect they had COVID-19 take the finger-prick test themselves and photograph the result for a doctor to check. The study also tracks how receiving the test result changes participants' social distancing behavior and anxiety over eight weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Premier Biotech COVID-19 IgG/IgM Rapid Test Cassette, a finger-prick antibody test
- What this could lead to
- If the test works at home, people could check their own COVID-19 antibody status without visiting a clinic, which may help them make informed decisions about social distancing.
- What could go wrong
- This is a small usability study, not a large trial of test accuracy. People may misread their own results, and the test itself has not been fully reviewed by the FDA. Results may not apply to other antibody tests or to people outside New York City.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Started
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Apr 2020
- Finished
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Aug 2020
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Reside and Currently in New York City * Does not have a blood clotting disease * Is not abnormally queasy about taking a blood sample * Not on any blood thinning medications * Able to consent * Willingness to take a blood sample * Confirmed of highly likely past infection with COVID-19 over 14 days ago and fully recovered
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
ProofPilot Online App (https://p.proofpilot.com)
New York, New York, 10003, United States
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Other studies related to the condition(s) this trial covers.
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