Which Benefits Can Justify Risks in Research?
Publication date
2025
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Abstract
Research ethics committees (RECs) evaluate whether the risk-benefit ratio of a study is acceptable. Decentralized clinical trials (DCTs) are a novel approach for conducting clinical trials that potentially bring important benefits for research, including several collateral benefits. The position of collateral benefits in risk-benefit assessments is currently unclear. DCTs raise therefore questions about how these benefits should be assessed. This paper aims to reconsider the different types of research benefits, and their position in risk-benefit assessments. We first propose a categorization of research benefits, based on the types of benefits that can be distinguished from the literature and ethical guidelines. Secondly, we will reconsider the position of collateral benefits. We argue that these benefits are not fundamentally different from other benefits of research and can therefore be included in risk-benefit assessments of DCTs.
Keywords
Ethics committees, IRB (Institutional Review Board), decentralized clinical trials, research benefits, research ethics, risk/benefit analysis, Health Policy, Issues, ethics and legal aspects, SDG 3 - Good Health and Well-being
Citation
Trials@Home Consortium, van Rijssel, T I, van Thiel, G J M W, Gardarsdottir, H & van Delden, J J M 2025, 'Which Benefits Can Justify Risks in Research?', American Journal of Bioethics, vol. 25, no. 5, pp. 65-75. https://doi.org/10.1080/15265161.2023.2296404