Checklist to assess Trustworthiness in RAndomised Controlled Trials (TRACT checklist): concept proposal and pilot.

IF 7.2 Q1 ETHICS
Ben W Mol, Shimona Lai, Ayesha Rahim, Esmée M Bordewijk, Rui Wang, Rik van Eekelen, Lyle C Gurrin, Jim G Thornton, Madelon van Wely, Wentao Li
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Abstract

Objectives: To propose a checklist that can be used to assess trustworthiness of randomized controlled trials (RCTs).

Design: A screening tool was developed using the four-stage approach proposed by Moher et al. This included defining the scope, reviewing the evidence base, suggesting a list of items from piloting, and holding a consensus meeting. The initial checklist was set-up by a core group who had been involved in the assessment of problematic RCTs for several years. We piloted this in a consensus panel of several stakeholders, including health professionals, reviewers, journal editors, policymakers, researchers, and evidence-synthesis specialists. Each member was asked to score three articles with the checklist and the results were then discussed in consensus meetings.

Outcome: The Trustworthiness in RAndomised Clinical Trials (TRACT) checklist includes 19 items organised into seven domains that are applicable to every RCT: 1) Governance, 2) Author Group, 3) Plausibility of Intervention Usage, 4) Timeframe, 5) Drop-out Rates, 6) Baseline Characteristics, and 7) Outcomes. Each item can be answered as either no concerns, some concerns/no information, or major concerns. If a study is assessed and found to have a majority of items rated at a major concern level, then editors, reviewers or evidence synthesizers should consider a more thorough investigation, including assessment of original individual participant data.

Conclusions: The TRACT checklist is the first checklist developed specifically to detect trustworthiness issues in RCTs. It might help editors, publishers and researchers to screen for such issues in submitted or published RCTs in a transparent and replicable manner.

RAndomised Controlled Trials 可信度评估核对表(TRACT 核对表):概念提案和试点。
目的:提出一份可用于评估随机对照试验(RCT)可信度的核对表:提出一份可用于评估随机对照试验(RCT)可信度的核对表:筛选工具的开发采用了莫赫尔等人提出的四阶段方法,包括确定范围、审查证据基础、提出试点项目清单以及召开共识会议。最初的核对表是由一个核心小组制定的,他们多年来一直参与有问题 RCT 的评估工作。我们在一个由多个利益相关者组成的共识小组中进行了试点,其中包括医疗专业人士、审稿人、期刊编辑、政策制定者、研究人员和证据合成专家。每位成员都被要求用核对表给三篇文章打分,然后在共识会议上讨论结果:临床试验可信度(TRACT)核对表包括 19 个项目,分为七个领域,适用于每项临床试验:1)管理;2)作者群;3)干预措施使用的可信度;4)时间框架;5)辍学率;6)基线特征;7)结果。每个项目都可以回答为 "没有疑虑"、"有一些疑虑/没有信息 "或 "有重大疑虑"。如果对一项研究进行评估后发现大部分项目被评为重大问题,那么编辑、评审人员或证据综合人员应考虑进行更彻底的调查,包括评估原始的个体参与者数据:TRACT核对表是第一份专门用于检测RCT可信度问题的核对表。它可以帮助编辑、出版商和研究人员以透明、可复制的方式在提交或发表的 RCT 中筛查此类问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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