代表性问题:黑人前列腺癌患者对数字健康信息的信任
Stacy Loeb1,2,3, Tatiana Sanchez Nolasco1,2, Nataliya Byrne1,2
1Department of Urology, New York University School of Medicine, New York, New York.
The Journal of urology
|February 8, 2024
概括
黑人前列腺癌 (PCa) 患者希望在在线健康信息中看到种族多样性. 对在线PCa内容的信任受到表现,来源可信度和网站专业性的影响.
科学领域:
- 卫生沟通健康沟通
- 在健康方面存在差异.
- 在瘤学瘤学.
背景情况:
- 互联网是美国成年人的健康信息的主要来源.
- 在线前列腺癌 (PCa) 信息质量差异很大.
- 黑人成年人面临更高的PCa发病率和死亡率,但在线代表性不足.
研究的目的:
- 探索黑人PCa患者对在线内容中的种族代表性的看法.
- 确定影响黑人患者对在线PCa信息信任的因素.
主要方法:
- 进行了7个虚拟焦点小组,其中包括被诊断患有PCa的黑人患者.
- 收集的人口统计数据和对选定的在线PCa内容的反.
- 使用常数比较定性方法分析焦点组成绩单.
主要成果:
- 大多数参与者利用在线资源获取PCa信息.
- 种族代表性对于建立对在线健康内容的信任至关重要.
- 缺乏黑人代表性导致误解和减少信息搜索;信誉良好的来源和专业网站增强信任.
结论:
- 黑人成年人在网上PCa内容中的代表性不足可能会加剧健康差异.
- 有效的在线健康沟通需要种族多样性,基于证据的内容和来自可信来源的专业陈述.
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