临床表现 临床表现
Jasmine Blane1,2, Shona Forster2, Anna Lucas3
1Oxford Health NHS Foundation Trust, Oxford, Oxfordshire, United Kingdom.
Alzheimer's & dementia : the journal of the Alzheimer's Association
|December 24, 2025
概括
患者和公众参与 (PPI) 是开发一种以患者为中心的痴呆症和轻度认知障碍的远程监测研究的关键. 这种方法确保了研究设计满足了患者对相关数据和参与选择的需求,提高了可行性.
科学领域:
- 神经学 神经学
- 数字健康数字健康
- 以患者为中心的护理
背景情况:
- 远程监控工具提供了有价值的数据,但在临床环境中面临可行性问题.
- 以患者为中心的设计对于记忆诊所的工具有效性和数据质量至关重要.
- 这项研究旨在将患者和公共参与 (PPI) 整合到为牛津大脑健康诊所开发远程监测研究中.
研究的目的:
- 在开发远程监控研究中系统地整合PPI.
- 确保研究设计以患者为中心,有效,并能被记忆诊所人群容忍.
- 通过共同设计的远程监控方法产生高质量的数据.
主要方法:
- 参与痴呆症,轻度认知障碍,亲属和痴呆症研究志愿者的个人.
- 利用研讨会,调查,用户测试,与非专业成员合作制作,以及PPI小组咨询.
- 包含关于研究相关性,评估选择和数字任务改进的反.
主要成果:
- PPI显著塑造了研究,强调了结果测量相关性和参与者选择.
- 确定的主要结果措施包括日常活动,记忆,人际关系和护理需求.
- 研究设计得到了改进,以最大限度地提高患者/亲属的选择,并纳入对数字和模拟评估的建议,这些评估被认为是可以接受和可行的.
结论:
- 整合PPI创建了一个以患者为中心的远程监测研究,与患者和相对需求保持一致.
- 对于临床人群的数字评估研究,挑战假设和改善结果,PPI是非常宝贵的.
- 这种方法提高了研究的可接受性,并促进了患者和亲属的更大包容性.
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