Department of Clinical Research, Basel Institute for Clinical Epidemiology and Biostatistics, University of Basel and University Hospital Basel, Basel, Switzerland.
Institute of History and Ethics in Medicine, TUM School of Medicine, Technical University of Munich, Munich, Germany.
JAMA Netw Open. 2021 Nov 1;4(11):e2136577. doi: 10.1001/jamanetworkopen.2021.36577.
A systematic assessment of existing research should justify the conduct and inform the design of new clinical research but is often lacking. There is little research on the barriers to and factors facilitating systematic evidence assessments.
To examine the practices and attitudes of Swiss stakeholders and international funders regarding conducting systematic evidence assessments in academic clinical trials.
DESIGN, SETTING, AND PARTICIPANTS: In this qualitative study, individual semistructured qualitative interviews were conducted between February and August 2020 with 48 Swiss stakeholder groups (27 primary investigators, 9 funders and sponsors, 6 clinical trial support organizations, and 6 ethics committee members) and between January and March 2021 with 9 international funders of clinical trials from North America and Europe with a reputation for requiring systematic evidence synthesis in applications for academic clinical trials.
The main outcomes were practices and attitudes of Swiss stakeholders and international funders regarding conducting systematic evidence assessments in academic clinical trials. Interviews were analyzed using conventional content analysis.
Of the 57 participants, 40 (70.2%) were male. Participants universally acknowledged that a comprehensive understanding of the previous evidence is important but reported wide variation regarding how this should be achieved. Participants reported that the conduct of formal systematic reviews was currently not expected before most clinical trials, but most international funders reported expecting a systematic search for the existing evidence. Whereas time and resources were reported by all participants as barriers to conducting systematic reviews, the Swiss research ecosystem was reported not to be as supportive of a systematic approach compared with international settings.
In this qualitative study, Swiss stakeholders and international funders generally agreed that new clinical trials should be justified by a systematic evidence assessment but that barriers on individual, organizational, and political levels kept them from implementing it. More explicit requirements from funders appear to be needed to clarify the required level of comprehensiveness in summarizing existing evidence for different types of clinical trials.
系统评估现有研究对于证明新临床研究的合理性并为其设计提供信息至关重要,但这种评估往往缺乏。关于进行系统证据评估的障碍和促进因素的研究很少。
调查瑞士利益相关者和国际资助者在学术临床试验中进行系统证据评估的实践和态度。
设计、设置和参与者:在这项定性研究中,于 2020 年 2 月至 8 月期间对 48 个瑞士利益相关者群体(27 名主要研究者、9 名资助者和赞助商、6 个临床试验支持组织和 6 名伦理委员会成员)进行了个体半结构化定性访谈,并于 2021 年 1 月至 3 月对来自北美和欧洲的 9 家有要求在学术临床试验申请中进行系统证据综合的声誉的国际临床试验资助者进行了访谈。
主要结果是瑞士利益相关者和国际资助者在学术临床试验中进行系统证据评估的实践和态度。访谈使用常规内容分析进行分析。
在 57 名参与者中,有 40 名(70.2%)为男性。参与者普遍承认全面了解以前的证据很重要,但报告说如何实现这一点存在广泛差异。参与者报告说,在大多数临床试验之前,目前不期望进行正式的系统评价,但大多数国际资助者报告说期望对现有证据进行系统搜索。所有参与者都报告说,时间和资源是进行系统评价的障碍,但与国际环境相比,瑞士研究生态系统被报告为不那么支持系统方法。
在这项定性研究中,瑞士利益相关者和国际资助者普遍同意,新的临床试验应该通过系统的证据评估来证明其合理性,但个人、组织和政治层面的障碍使他们无法实施。资助者似乎需要更明确的要求,以明确为不同类型的临床试验总结现有证据所需的全面程度。