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Reporting of sex and gender in randomized controlled trials in Canada: a cross-sectional methods study

机译:加拿大随机对照试验中性别的报告:横断面研究

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BackgroundAccurate reporting on sex and gender in health research is integral to ensuring that health interventions are safe and effective. In Canada and internationally, governments, research organizations, journal editors, and health agencies have called for more inclusive research, provision of sex-disaggregated data, and the integration of sex and gender analysis throughout the research process. Sex and gender analysis is generally defined as an approach for considering how and why different subpopulations (e.g., of diverse genders, ages, and social locations) may experience health conditions and interventions in different or similar ways.The objective of this study was to assess the extent and nature of reporting about sex and/or gender, including whether sex and gender analysis (SGA) was carried out in a sample of Canadian randomized controlled trials (RCTs) with human participants.MethodsWe searched MEDLINE from 01 January 2013 to 23 July 2014 using a validated filter for identification of RCTs, combined with terms related to Canada. Two reviewers screened the search results to identify the first 100 RCTs that were either identified in the trial publication as funded by a Canadian organization or which had a first or last author based in Canada. Data were independently extracted by two people from 10% of the RCTs during an initial training period; once agreement was reached on this sample, the remainder of the data extraction was completed by one person and verified by a second.ResultsThe search yielded 1433 records. We screened 256 records to identify 100 RCTs which met our eligibility criteria. The median sample size of the RCTs was 107 participants (range 12–6085). While 98% of studies described the demographic composition of their participants by sex, only 6% conducted a subgroup analysis across sex and 4% reported sex-disaggregated data. No article defined “sex” and/or “gender.” No publication carried out a comprehensive sex and gender analysis.ConclusionsFindings highlight poor uptake of sex and gender considerations in the Canadian RCT context and underscore the need for better articulated guidance on sex and gender analysis to improve reporting of evidence, inform policy development, and guide future research.
机译:背景技术在健康研究中准确报告性别和性别,对于确保健康干预措施安全有效是不可或缺的。在加拿大和国际上,政府,研究组织,期刊编辑和卫生机构都呼吁开展更具包容性的研究,提供按性别分类的数据,并在整个研究过程中整合性别分析。性别分析通常被定义为一种方法,用于考虑不同亚人群(例如,不同性别,年龄和社会位置)如何以及为什么以不同或相似的方式经历健康状况和干预措施。本研究的目的是评估方法从2013年1月1日至7月23日在MEDLINE中进行搜索,包括关于性别的报告的范围和性质,包括是否在加拿大随机对照试验(RCT)样本中对性别和性别分析(SGA)进行了研究。 2014年,使用经过验证的过滤器来识别RCT,并结合了与加拿大有关的术语。两名审阅者筛选了搜索结果,以确定前100个RCT,这些RCT在试验出版物中被确定为由加拿大组织资助,或第一作者或最后作者位于加拿大。在最初的培训期间,由两个人从10%的RCT中独立提取数据;一旦对该样本达成协议,剩下的数据提取工作将由一个人完成,并经过一秒钟的验证。结果搜索产生了1433条记录。我们筛选了256条记录,以确定100个符合我们资格标准的RCT。 RCT的中位样本量为107名参与者(范围12–6085)。尽管98%的研究按性别描述了参与者的人口统计学组成,但只有6%的研究按性别进行了亚组分析,而4%的研究报告了按性别分类的数据。没有文章定义“性别”和/或“性别”。没有出版物进行全面的性别和性别分析。结论研究结果强调了加拿大RCT背景下对性别和性别的考虑不佳,并强调需要针对性别和性别分析提供更好的明确指导,以改善证据报告,为政策制定和指南提供指导未来的研究。

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