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外科试点随机对照试验报告质量(REPORTS):一项方法学调查方案

REporting quality of PilOt randomised controlled trials in surgery (REPORTS): a methodological survey protocol.

作者信息

McKechnie Tyler, Kazi Tania, Wang Austine, Zhang Sophia, Thabane Alex, Nanji Keean, Doumouras Aristithes G, Eskicioglu Cagla, Thabane Lehana, Parpia Sameer, Bhandari Mohit

机构信息

Department of Surgery, McMaster University, Hamilton, Ontario, Canada

Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.

出版信息

BMJ Open. 2024 Apr 23;14(4):e085293. doi: 10.1136/bmjopen-2024-085293.

Abstract

INTRODUCTION

The aim of this methodological review is to evaluate the completeness of reporting of surgical pilot and feasibility randomised trials as per the Consolidated Standards of Reporting Trials (CONSORT) extension to randomised pilot and feasibility trials. Moreover, we aim to assess for the presence of spin reporting and inconsistency between abstract and main text reporting in surgical pilot and feasibility randomised trials.

METHODS AND ANALYSIS

A comprehensive, electronic search strategy will be used to identify studies indexed in Medline, Embase and Cochrane Central Register of Controlled Trials (CENTRAL) databases. Studies will be included if they are pilot or feasibility randomised trials of surgical interventions. The primary outcome will be overall CONSORT statement extension to randomised pilot and feasibility trials checklist completeness. This will be defined as trials reporting each of the 40 items in the CONSORT statement extension to randomised pilot and feasibility trials checklist. Secondary outcomes will include the reporting of individual studies as per the CONSORT extension to randomised pilot and feasibility trials, the use of spin reporting strategies, trial factors associated with reporting quality and spin strategy use, and consistency between abstract and main text reporting. Poisson and logistic regressions will be performed to explore the association between trial factors and completeness of reporting as measured by the number of reported CONSORT items.

ETHICS AND DISSEMINATION

This is a methodological survey that has been registered a priori on the International Prospective Register for Systematic Reviews (PROSPERO) (CRD42023475512). Local ethics approval is not required. We plan to disseminate study results through peer-reviewed publication and conference presentations.

摘要

引言

本方法学综述的目的是根据随机试验报告的统一标准(CONSORT)对随机试点和可行性试验的扩展,评估外科试点和可行性随机试验报告的完整性。此外,我们旨在评估外科试点和可行性随机试验中是否存在夸大性报告以及摘要与正文报告之间的不一致性。

方法与分析

将采用全面的电子检索策略,以识别在Medline、Embase和Cochrane对照试验中央注册库(CENTRAL)数据库中索引的研究。如果研究是外科干预的试点或可行性随机试验,则将其纳入。主要结局将是CONSORT声明对随机试点和可行性试验扩展清单的整体完整性。这将定义为在CONSORT声明对随机试点和可行性试验扩展清单中报告40项中的每一项的试验。次要结局将包括根据CONSORT对随机试点和可行性试验的扩展对个体研究的报告、夸大性报告策略的使用、与报告质量和夸大性策略使用相关的试验因素,以及摘要与正文报告之间的一致性。将进行泊松回归和逻辑回归,以探讨试验因素与以报告的CONSORT项目数量衡量的报告完整性之间的关联。

伦理与传播

这是一项方法学调查,已事先在国际前瞻性系统评价注册库(PROSPERO)(CRD42023475512)上注册。无需当地伦理批准。我们计划通过同行评审出版物和会议报告来传播研究结果。

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