Connie M Ulrich,Christine Grady,George Demiris et al.
Connie M Ulrich et al.
Privacy and confidentiality of personal medical information are cornerstones of ethical clinical care and ethical research. But real-world research has challenged traditional ways of thinking about privacy and confidentiality of information...
Case Reports
Ethics & human research. 2021 Jan;43(1):25-31. DOI:10.1002/eahr.500076 2021
Published Erratum
Ethics & human research. 2020 Nov;42(6):20. DOI:10.1002/eahr.500070 2020
Ethical Considerations When Using a Mobile Eye Tracker in a Patient-Facing Area: Lessons from an Intensive Care Unit Observational Protocol [0.03%]
在患者区域使用移动眼动仪时的伦理考量——来自重症监护病房观察计划的经验教训
Ethan P Larsen,Jacob M Kolman,Faisal N Masud et al.
Ethan P Larsen et al.
This article describes the process of designing, approving, and conducting an investigator-initiated protocol to use an eye-tracking device in a health care setting. Participants wore the device, which resembles eyeglasses, in a front-facin...
Observational Study
Ethics & human research. 2020 Nov;42(6):2-13. DOI:10.1002/eahr.500068 2020
Loopholes in the Research Ethics System? Informed Consent Waivers in Cluster Randomized Trials with Individual-Level Intervention [0.03%]
群随机试验中免除知情同意书的现象及伦理审校系统中的漏洞？以个体层面干预为例
Alex John London,Monica Taljaard,Charles Weijer
Alex John London
Individual-cluster trials randomize groups of individuals but deliver study interventions directly to individual participants. We examine three arguments that might justify the perception that the bar for a waiver of consent should be lower...
Benefit Sharing for Human Genomics Research: Awareness and Expectations of Genomics Researchers in Sub-Saharan Africa [0.03%]
撒哈拉以南非洲基因组学研究人员的利益共享意识及其期望：基因组研究利益分享机制探究
Nchangwi Syntia Munung,Jantina de Vries
Nchangwi Syntia Munung
Benefit sharing is an ethical issue that underscores the need to find a balance between access to genetic resources and the provision of fair benefits in exchange for access. The Human Genome Organisation (HUGO) is one of the few initiative...
Ethical and Practical Concerns about IRB Restrictions on the Use of Research Data [0.03%]
伦理学和实践中的IRB对研究数据使用限制的担忧
Mark Barnes,Judith Carrithers,Jeremy Sugarman
Mark Barnes
In response to researcher noncompliance with ethical and regulatory provisions governing research with humans, protocol deviations, and unanticipated problems with research, institutional review boards (IRBs) or institutions sometimes impos...
Thought Leader Comparisons of Risks in Precision Medicine Research [0.03%]
精准医学研究中的风险比较及相关性——思想领导者的观点
Laura M Beskow,Catherine M Hammack-Aviran,Kathleen M Brelsford
Laura M Beskow
Biomedical research is increasingly capitalizing on an array of data to illuminate the interplay between "omics," lifestyle, and health. Leveraging this information presents opportunities to advance knowledge but also poses risks to researc...
Big Data, Biomedical Research, and Ethics Review: New Challenges for IRBs [0.03%]
大数据、生物医学研究及伦理审查：IRB面临的新的挑战
Agata Ferretti,Marcello Ienca,Samia Hurst et al.
Agata Ferretti et al.
The increased use of big data in the medical field has shifted the way in which biomedical research is designed and carried out. The novelty of techniques and methods brought by big data research brings new challenges to institutional revie...
Ethical and Regulatory Concerns in Pragmatic Clinical Trial Monitoring and Oversight [0.03%]
务实临床试验监控和监管中的伦理及法规关注点
Michelle K Roberts,Dylan M Fisher,Lea E Parker et al.
Michelle K Roberts et al.
The implementation of pragmatic clinical trials (PCTs) can be accompanied by unique regulatory challenges. In this paper, we describe the experience and management of regulatory noncompliance during a 25-site acute care PCT. During the tria...
Published Erratum
Ethics & human research. 2020 Sep;42(5):16. DOI:10.1002/eahr.500063 2020