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Klinische Studie

At-Home COVID-19 Antibody Test Usability Assessment & Behavior Change Study

NCT: NCT04393961 · WITHDRAWN

NCT-IDNCT04393961
Medizinische Daten: StatusWITHDRAWN
Startdatum2020-04-05
Abschluss2020-08-29
SponsorProofPilot (INDUSTRY)
First posted
Last updated

Kurzzusammenfassung

Radish Health and ProofPilot in coordination with Sanesco are running this study to help establish whether the Premier Biotech COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma Authorized for distribution under emergency use authorization - though not yet FDA reviewed) can be conducted effectively at home to detect COVID-19 antibodies among individuals who have tested positive, or suspect they have previous contracted from COVID-19 and recovered. The study also aims to examine how the results of those tests change social-distancing behaviors and general anxiety over 8 weeks post-test.

Offizielle Quelle

Auf ClinicalTrials.gov ansehen →

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