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

IF 7.2 Q1 ETHICS Research integrity and peer review Pub Date : 2017-09-01 eCollection Date: 2017-01-01 DOI:10.1186/s41073-017-0039-6
V Welch, M Doull, M Yoganathan, J Jull, M Boscoe, S E Coen, Z Marshall, J Pardo Pardo, A Pederson, J Petkovic, L Puil, L Quinlan, B Shea, T Rader, V Runnels, S Tudiver
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Abstract

Background: Accurate 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.

Methods: We 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.

Results: The 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.

Conclusions: Findings 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.

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加拿大随机对照试验中的性别报告:横断面方法研究。
背景:准确报告健康研究中的性和性别问题,是确保健康干预措施安全有效的必要条件。在加拿大和国际上,各国政府、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,提供按性别分列的数据,并在整个研究过程中融入性与性别分析。本研究的目的是评估有关性和/或性别的报告的范围和性质,包括是否在有人类参与者的加拿大随机对照试验(RCT)样本中进行了性和性别分析(SGA):我们使用经过验证的 RCT 识别过滤器,结合与加拿大相关的术语,检索了 2013 年 1 月 1 日至 2014 年 7 月 23 日的 MEDLINE。两名审稿人对搜索结果进行筛选,以确定前 100 项 RCT,这些 RCT 要么在试验出版物中被确认为由加拿大组织资助,要么其第一作者或最后作者位于加拿大。在最初的培训期间,两人分别从 10% 的 RCT 中独立提取数据;在就这一样本达成一致后,由一人完成剩余数据的提取,并由另一人进行核实:搜索共获得 1433 条记录。我们筛选了 256 条记录,确定了 100 项符合资格标准的 RCT。RCT 的样本量中位数为 107 名参与者(范围为 12-6085 人)。虽然 98% 的研究按性别描述了参与者的人口构成,但只有 6% 的研究进行了不同性别的亚组分析,4% 的研究报告了按性别分列的数据。没有一篇文章定义了 "性 "和/或 "性别"。没有一篇文章对 "性 "和/或 "性别 "进行了定义:研究结果表明,在加拿大的 RCT 研究中,对性别和社会性别的考虑较少,并强调需要更好地阐明性别和社会性别的分析指南,以改进证据报告、为政策制定提供信息并指导未来的研究。
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