在疼痛研究中标准化社会人口统计数据收集:为最低数据集引入共识建议
Emma L Karran1, Aidan G Cashin2, Alessandro Chiarotto3
1The 'Identifying Social Factors that Stratify Health Opportunities and Outcomes' (ISSHOOS) Collaboration Core Research Group, Australia; IIMPACT in Health, University of South Australia, Kaurna Country, Adelaide, South Australia, Australia.
The journal of pain
|December 25, 2025
概括
ISSHOOs项目为收集疼痛研究中的社会人口统计数据提供了新的建议. 这旨在提高研究完整性,并促进疼痛患者的健康公平.
科学领域:
- 医疗保健服务研究 医疗服务研究
- 疼痛医学 医学 疼痛医学
- 健康 公平 卫生 公平
背景情况:
- 在疼痛研究中不一致的社会人口统计数据收集阻碍了健康公平.
- 以前的数据收集方法缺乏标准化和全球相关性.
研究的目的:
- 为在人类成人疼痛研究中收集社会人口统计数据提出共识推.
- 为了使收集股权相关信息的最低数据集变得可操作.
- 促进疼痛研究的透明度,诚信和价值.
主要方法:
- 由ISSHOOs (确定分层化健康机会和结果的社会因素) 项目开发的共识推.
- 开发一个最小数据集 (A数据集) 和一个扩展的可选数据集 (B数据集).
- 实施考虑因素,好处和潜在危害的审查.
主要成果:
- 发表的建议为数据收集提供了一个全球相关和可适应的资源.
- 这些建议使收集与股权相关的基本信息变得更有效.
- 一个单独的手稿提供了关于建议的详细解释和阐述.
结论:
- 常规采用ISSHOO的建议可以提高研究的透明度和完整性.
- 实施这些建议有可能促进疼痛患者的健康公平.
- ISSHOOs合作旨在在研究实践中进行广泛的转变,以提高研究价值.
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