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Challenges and proposed solutions in making clinical research on COVID-19 ethical: a status quo analysis across German research ethics committees

机译:Covid-19道德临床研究挑战和提出的解决方案:德国研究伦理委员会的现状分析

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In the course of the COVID-19 pandemic, the biomedical research community’s attempt to focus the attention on fighting COVID-19, led to several challenges within the field of research ethics. However, we know little about the practical relevance of these challenges for Research Ethics Committees (RECs). We conducted a qualitative survey across all 52 German RECs on the challenges and potential solutions with reviewing proposals for COVID-19 studies. We de-identified the answers and applied thematic text analysis for the extraction and synthesis of challenges and potential solutions that we grouped under established principles for clinical research ethics. We received an overall response rate of 42%. The 22 responding RECs reported that they had assessed a total of 441 study proposals on COVID-19 until 21 April 2020. For the review of these proposals the RECs indicated a broad spectrum of challenges regarding (1) social value (e.g. lack of coordination), (2) scientific validity (e.g. provisional study planning), (3) favourable risk–benefit ratio (e.g. difficult benefit assessment), (4) informed consent (e.g. strict isolation measures), (5) independent review (e.g. lack of time), (6) fair selection of trial participants (e.g. inclusion of vulnerable groups), and (7) respect for study participants (e.g. data security). Mentioned solutions ranged from improved local/national coordination, over guidance on modified consent procedures, to priority setting across clinical studies. RECs are facing a broad spectrum of pressing challenges in reviewing COVID-19 studies. Some challenges for consent procedures are well known from research in intensive care settings but are further aggravated by infection measures. Other challenges such as reviewing several clinical studies at the same time that potentially compete for the recruitment of in-house COVID-19 patients are unique to the current situation. For some of the challenges the proposed solutions in our survey could relatively easy be translated into practice. Others need further conceptual and empirical research. Our findings together with the increasing body of literature on COVID-19 research ethics, and further stakeholder engagement should inform the development of hands-on guidance for researchers, funders, RECs, and further oversight bodies.
机译:在Covid-19大流行过程中,生物医学研究界的尝试将注意力集中在战斗Covid-19上,导致了研究道德领域的几个挑战。然而,我们对这些挑战对研究伦理委员会(REC)的实际相关性知之甚少。我们对所有52名德国德国勘犯进行了定性调查,审查了Covid-19研究的提案。我们通过确定在临床研究道德的既定原则下分组的挑战和潜在解决方案的提取和综合答案和应用主题文本分析。我们收到了42%的整体反应率。 22次响应的康复报告称,他们在2020年4月21日之前评估了Covid-19上的441个研究提案。对于这些提案,REC表示关于(1)社会价值的广泛挑战(例如缺乏协调) ,(2)科学有效性(例如临时研究规划),(3)有利的风险效益比(例如困难福利评估),(4)知情同意(例如严格的隔离措施),(5)独立审查(例如缺乏时间),(6)审判参与者的公平选择(例如包含弱势群体),(7)尊重研究参与者(例如数据安全)。提到的解决方案范围从改善的地方/国家协调,关于修改的同意程序的指导,临床研究的优先设定。 REC在审查Covid-19研究时面临着广泛的压迫挑战。同意程序的一些挑战是从重症监护环境的研究中众所周知的,但进一步因感染措施而加剧。其他挑战,如审查几项临床研究,同时可能竞争内部Covid-19患者的招聘是当前情况的独特之处。对于一些挑战,我们调查中的提议解决方案可能相对容易地翻译成实践。其他人需要进一步的概念和实证研究。我们的调查结果与Covid-19研究道德的越来越多的文学体验,进一步的利益相关者参与应该告知研究人员,资助者,休会和进一步监督机构的动手指导。

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