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This cohort study received approval from the Johns Hopkins University School of Medicine Institutional Review Board. No informed consent was obtained because the study used de[-]identified data. We followed the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline.
archived "COVID-related" behavioral study
I participated in this weekly, web-based survey for ~ 10 months, and not one questionnaire--not even the initial Rx screening--queried ADRs. It was a tiresome, repetitive template. But let's presume Rx initial Rx screening (no immuno-mudulating regimen) and subsequent COVID-pos contact tracing, symptom queries as well as Likert "mood" traps (none) excluded my exposure to A/B conditional testing: I withdrew from the exercise with the distinct impression it was a wasted opportunity.  
by Cat on Thu Dec 30th, 2021 at 05:54:59 PM EST
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