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What are the roles and valued attributes of a Trial Steering Committee? Ethnographic study of eight clinical trials facing challenges

机译:审判指导委员会的作用和重要属性是什么?人种学研究面临挑战的八项临床试验

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Background Clinical trials oversight by a Trial Steering Committee (TSC) is mandated by Good Clinical Practice. This study used qualitative methods to explore the role and valued attributes of the TSC to inform planned updates of Medical Research Council guidance and TSC terms of reference. Methods An ethnographic study was conducted during 2013–2014. TSC and Trial Management Group meetings from eight trials were observed and audio-recorded, and semi-structured interviews conducted with purposively sampled key informants: independent and non-independent TSC members, trial sponsor representatives, funder representatives and chief investigators. The selected trials were currently recruiting and dealing with challenging scenarios. Data were analysed thematically and findings triangulated and integrated to give a multi-perspective account of the role and valued attributes of a TSC. Results Eight TSC meetings and six Trial Management Group meetings were observed. Sixty-five interviews were conducted with 51 informants. The two main roles played by the TSC were quality assurance and patient advocacy. Quality assurance involved being a ‘critical friend’ or a provider of ‘tough love’. Factors influencing the ability of the TSC to fulfil this role included the TSC Chair, other independent TSC members and the model of the TSC and its fit with the trial subject. The role of the TSC as an advocate for patient well-being was perceived as paramount. Two attributes of TSC members emerged as critical: experience (of running a trial, trial oversight or in a clinical/methodological area) and independence. While independence was valued for giving impartiality, the lack of consensus about its definition and strict requirements of some funders made it difficult to operationalise. Conclusions We found tensions and ambiguities in the roles expected of TSCs and the attributes valued of TSC members. In particular, the requirements of independence and experience could conflict, impacting the TSCs’ quality assurance role. Concerns were raised regarding whose interests are served by funders’ criteria of independence; in particular, funders’ selection of TSC members was thought to potentially inhibit TSCs’ ability to fulfil their patient advocacy role. These findings should be incorporated in revising guidance and terms of reference for TSCs.
机译:背景技术良好临床实践要求临床试验指导委员会(TSC)对临床试验进行监督。这项研究使用定性方法来探索TSC的作用和有价值的属性,从而为医学研究理事会指南和TSC职责范围的计划更新提供信息。方法在2013–2014年期间进行了民族志研究。观察并记录了来自8个试验的TSC和审判管理小组会议,并进行了录音,并有针对性地抽样了关键信息提供者:独立和非独立的TSC成员,试验保荐人代表,出资者代表和首席调查员。所选试验目前正在招募并处理具有挑战性的方案。对数据进行了主题分析,并对发现进行了三角化和整合,从而对TSC的作用和有价值的属性进行了多角度分析。结果观察到8次TSC会议和6次审判管理小组会议。对51位线人进行了65次访谈。 TSC扮演的两个主要角色是质量保证和患者倡导。质量保证涉及成为“关键朋友”或“坚强的爱人”的提供者。影响TSC履行此职责能力的因素包括TSC主席,其他TSC独立成员以及TSC的模式及其与试验对象的适应性。 TSC作为倡导患者福祉的角色被认为至关重要。 TSC成员的两个属性显得至关重要:经验(进行试验,进行试验监督或在临床/方法学领域)和独立性。尽管重视独立性是为了赋予公正性,但由于缺乏独立性的定义和一些出资者的严格要求,使其难以运作。结论我们发现在TSC的期望角色和TSC成员的价值观方面存在紧张和模棱两可的情况。特别是,独立性和经验的要求可能会发生冲突,从而影响TSC的质量保证角色。提出了关于资助者的独立性标准为谁的利益服务的担忧;特别是,人们认为资助者选择TSC成员可能会抑制TSC履行其患者倡导角色的能力。这些发现应纳入修订TSC的指南和职责范围中。

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