亨廷顿病患者对自己的疾病的看法:在线直接对参与者进行的试点研究
Karen E Anderson1, Lakshmi Arbatti2, Abhishek Hosamath2
1Georgetown University, Washington, DC, USA.
Journal of Huntington's disease
|May 3, 2024
概括
在线数据收集对于亨廷顿病是可行的.
科学领域:
- 临床研究方法论 临床研究方法论
- 神经退行性疾病 神经退行性疾病
- 数字健康数字健康
背景情况:
- 直接向参与者进行在线报告可以提高临床研究的可访问性和患者参与度.
- 在线平台使研究研究中的有效数据收集和患者报告的结果成为可能.
研究的目的:
- 评估从被诊断患有亨廷顿病的成年人中在线数据收集的可行性.
- 通过直接在线报告来捕捉患者报告的问题和功能影响.
主要方法:
- 从被诊断患有亨廷顿病的美国居民收集在线数据,满足移动性和自给自足标准.
- 利用亨廷顿研究小组的myHDstory平台和亨廷顿病患者问题报告 (HD-PROP) 问卷.
- 采用自然语言处理,专家策划和机器学习来分类患者报告的症状.
主要成果:
- 345名参与者完成了在线试点研究;60.9%是男性,平均年龄为34.5岁和自诊断以来的9.5岁.
- 报道了各种种族自我认同,包括高加索人,非裔美国人和美洲印第安人/阿拉斯加土著参与者.
- 非运动性症状,特别是抑郁症和认知障碍是最常见的问题.
结论:
- 在线研究参与对于各种各样的亨廷顿病队伍是可行的,突出非运动症状.
- 在线工具有效地捕捉了患者的担忧,并确定了有意义的临床结果.
- 数字研究促进了多样化和代表性不足的人群参与亨廷顿病研究.
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