A checklist to evaluate a report of a nonpharmacological trial (CLEAR NPT) was developed using consensus

被引:221
作者
Boutron, I [1 ]
Moher, D
Tugwell, P
Giraudeau, B
Poiraudeau, S
Nizard, R
Ravaud, P
机构
[1] INSERM, U738, F-75018 Paris, France
[2] Grp Hosp Bichat Claude Bernard, Dept Epidemiol Biostat & Rech Clin, F-75877 Paris, France
[3] Univ Paris 07, Fac Xavier Bichat, F-75018 Paris, France
[4] Univ Ottawa, Fac Med, Dept Pediat, Ottawa, ON, Canada
[5] INSERM, CIC 202, Tours, France
[6] Childrens Hosp Eastern Ontario, Inst Res, Ctr Climate & Global Change Res, Chalmers Res Grp, Ottawa, ON K1H 8L1, Canada
[7] Univ Paris 05, Hop Cochin, APHP, Dept Med Phys & Readaptat, F-75270 Paris, France
[8] Univ Paris 07, Hop Lariboisiere, Serv Orthopedie, APHP, Paris, France
关键词
randomized controlled trials; quality assurance; surgery; rehabilitation therapy; psychotherapy; education; meta-analysis;
D O I
10.1016/j.jclinepi.2005.05.004
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background and Objective: To develop a checklist of items measuring the quality of reports of randomized clinical trials (RCTs) assessing nonpharmacological treatments (NPTs). Study Design and Setting: The Delphi consensus method was used to select and reduce the number of items in the checklist. A total of 154 individuals were invited to participate: epidemiologists and statisticians involved in the field of methodology of RCTs (n = 55), members of the Cochrane Collaboration (n = 41), and clinicians involved in planning NPT clinical trials (n = 58). Participants ranked on a 10-point Likert scale whether an item should be included in the checklist. Results: Fifty-five experts (36%) participated in the survey. They were experienced in systematic reviews (68% were involved in the Cochrane Collaboration) and in planning RCTs (76%). Three rounds of the Delphi method were conducted to achieve consensus. The final checklist contains 10 items and 5 subiterns, with items related to the standardization of the intervention, care provider influence, and additional measures to minimize the potential bias from lack of blinding of participants, care providers, and outcome assessors. Conclusions: This tool can be used to critically appraise the medical literature, design NPT studies, and assess the quality of trial reports included in systematic reviews. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1233 / 1240
页数:8
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