Senior lecturer in the Department of Epidemiology and Biostatistics at the University of Zambia School of Public Health and is also the director of the Tropical Diseases Research Centre.
Associate professor in the Department of International Health at the Bloomberg School of Public Health and a core faculty member and the associate director for Global Programs at the Berman Institute of Bioethics at Johns Hopkins University.
Ethics Hum Res. 2023 Sep-Oct;45(5):2-14. doi: 10.1002/eahr.500178.
Over recent decades, adaptive trial designs have been used more and more often for clinical trials, including randomized controlled trials (RCTs). This rise in the use of adaptive RCTs has been accompanied by debates about whether such trials offer ethical and methodological advantages over traditional, fixed RCTs. This study examined how experts on clinical trial methods and ethics believe that adaptive RCTs, compared to fixed ones, affect the ethical character of clinical research. We conducted in-depth interviews with 17 researchers from bioethics, epidemiology, biostatistics, and/or medical backgrounds. While about half believed that adaptive trials are more complex and may thus threaten autonomy, these respondents also expressed that this challenge is not insurmountable. Most respondents expressed that efficiency and potential for participant benefit were the main justifications for adaptive trials. There was tension about whether adaptive randomization in response to increasing information disrupts clinical equipoise, with some respondents insisting that uncertainty still exists and therefore clinical equipoise is not disrupted. These findings suggest that further discussion is needed to increase the awareness and utility of these study designs.
近几十年来,适应性试验设计越来越多地用于临床试验,包括随机对照试验(RCT)。随着适应性 RCT 的使用增加,也出现了关于此类试验是否比传统的固定 RCT 具有伦理和方法学优势的争论。本研究考察了临床试验方法和伦理方面的专家如何认为,与固定 RCT 相比,适应性 RCT 会如何影响临床研究的伦理性质。我们对来自生物伦理学、流行病学、生物统计学和/或医学背景的 17 名研究人员进行了深入访谈。虽然大约一半的受访者认为适应性试验更复杂,因此可能会威胁到自主性,但这些受访者也表示,这种挑战并非不可逾越。大多数受访者表示,效率和潜在的参与者受益是采用适应性试验的主要理由。对于适应性随机化是否会因信息增加而破坏临床均衡存在争议,一些受访者坚持认为仍然存在不确定性,因此临床均衡没有被破坏。这些发现表明,需要进一步讨论以提高对这些研究设计的认识和实用性。