巴西东北地区对汉森氏病的看法:基于社区的研究,整合了耻辱,赋权和社会距离
Jaqueline Caracas Barbosa1, Aymée Medeiros da Rocha1,2,3, Hellen Xavier Oliveira2
1Postgraduate Program in Public Health, Faculty of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Tropical medicine & international health : TM & IH
|February 26, 2026
概括
对汉森氏病 (HD) 的知识不足有助于社区的耻辱和对受影响个人的负面态度. 健康教育对于改善理解和减少对患有HD的人的偏见至关重要.
科学领域:
- 公共卫生 公共卫生
- 社会科学 社会科学 社会科学
- 医学社会学 医学社会学
背景情况:
- 对汉森氏病 (HD) 的看法显著影响了耻辱,赋权和社交距离行为.
- 知识,态度和信仰是这些感知的关键决定因素.
- 了解这些因素对于开发有效的干预措施至关重要.
研究的目的:
- 调查关于汉森病 (HD) 关于耻辱和赋权的看法.
- 分析HD的知识,态度,信仰和感知之间的关系.
- 识别影响社会距离和受影响个人和社区赋权的因素.
主要方法:
- 在塞拉的特有社区进行了一项横截面的混合方法研究.
- 调查对1,309名参与者进行了调查,包括受影响的个人,接触者,社区成员和卫生工作者.
- 使用描述性统计和回归分析了定量数据,而定性数据则进行了主题分析.
主要成果:
- 社区成员对疾病知识较差,负面态度较强,社会距离得分较高.
- 社区卫生代理人 (CHA) 报告的污名化态度比社区成员更多.
- 受HD影响的个体感觉到高水平的耻辱和低的赋权.
结论:
- 在社区中,仍然存在重大知识差距和对HD的负面态度.
- 卫生保健教育和医疗保健专业人员的持续培训是必不可少的.
- 需要策略来打击耻辱和偏见,以提高对超越生物方面的理解.
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