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For that purpose, participants were randomly assigned (1:1 ratio) to prepare the drugs either with the support of the app (intervention group) or by conventional methods (control group). The trial protocols containing details of the scenarios have been previously published [36,37]. Both trials were performed in accordance with appropriate guidelines [38,39] and followed the CONSORT (Consolidated Standards of Reporting Trials) reporting guidelines [40].
JMIR Hum Factors 2022;9(1):e35399
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