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

被引:14
作者
Daykin, Anne [1 ]
Selman, Lucy E. [1 ]
Cramer, Helen [1 ]
McCann, Sharon [2 ]
Shorter, Gillian W. [3 ,4 ]
Sydes, Matthew R. [5 ,6 ]
Gamble, Carrol [7 ]
Macefield, Rhiannon [1 ]
Lane, J. Athene [1 ]
Shaw, Alison [1 ]
机构
[1] Univ Bristol, Sch Social & Community Med, MRC ConDuCT Hub Trials Methodol Res, Bristol BS8 2PS, Avon, England
[2] Univ Aberdeen, Hlth Serv Res Unit, Aberdeen AB25 2ZD, Scotland
[3] Trinity Coll Dublin, Sch Nursing & Midwifery, Trinity Ctr Practice & Healthcare Innovat, Belfast BT12 6BJ, Antrim, North Ireland
[4] Australian Natl Univ, ANU Coll Med Biol & Environm, Natl Inst Mental Hlth Res, GPO Box 4, Canberra, ACT 0200, Australia
[5] UCL, MRC Clin Trials Unit, London WC2B 6NH, England
[6] MRC London Hub Trial Methodol Res, London, England
[7] Univ Liverpool, Inst Translat Med, MRC North West Hub Trials Methodol Res, Liverpool L69 3BX, Merseyside, England
基金
英国医学研究理事会;
关键词
Randomised trials; Good clinical practice; Terms of reference; Trial Steering Committees; Trial monitoring;
D O I
10.1186/s13063-016-1425-y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
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页数:13
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