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ABSTRACT: Background
Enrolment is one of the most challenging aspects of conducting clinical trials, preceded by the process of informed consent (IC). Different strategies to improve recruitment in clinical trials have been used, including electronic IC. During COVID-19 pandemic, barriers to enrolment have been evident. Although digital technologies were acknowledged as the future of clinical research and potential advantages were shown for recruitment, electronic informed consent (e-IC) has not yet been globally adopted. The purpose of this review is to investigate the effect of using e-IC on enrolment, practical and economic benefits, challenges, and drawbacks when compared to traditional informed consent, through a systematic review.Methods
Embase, Global Health Library, Medline,
SUBMITTER: Mazzochi AT
PROVIDER: S-EPMC9942032 | biostudies-literature | 2023 Feb
REPOSITORIES: biostudies-literature