临床研究中的避孕要求 同意表格:评估和支持性别包容性实践
Tara Coffin1, Erin Brower1, Sharad Adekar1
1WCG IRB, Puyallup, WA, USA.
概括
临床试验同意表格经常使用性别语言,边缘化性别多元的个体. 虽然大多数形式包括一些性别包容性语言,但修订可以使它们完全包容,以便更好地参与研究.
科学领域:
- 临床研究伦理学
- 健康 公平 卫生 公平
- 医学术语 医学术语 医学术语
背景情况:
- 性别多样的人在临床研究中面临边缘化.
- 同意表格中的性别语言加剧了这个问题.
- 避孕要求是需要使用包容性语言的关键领域.
研究的目的:
- 评估在临床试验同意表格中使用性别包容性语言.
- 分析如何描述避孕要求.
- 确定改善语言包容性的障碍和机会.
主要方法:
- 对289份临床试验同意表格的内容分析.
- 用于分类的演和总结方法.
- 分析重点是描述避孕要求的语言.
主要成果:
- 79%的表格使用了一些性别包容性语言.
- 80%使用生物性语言,91%使用性别语言.
- 没有形式是完全包括性别的;大多数使用语言类型的混合.
结论:
- 临床试验同意表格显示了包容性和性别语言的混合.
- 在标题中排除生物性别引用可能会导致更具包容性的形式.
- 微小的修订可以显著提高同意过程中的性别包容性.
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