多模式融合智能家居和基于文本的行为标记,用于临床评估预测。

ACM transactions on computing for healthcare Pub Date : 2022-10-01 Epub Date: 2022-11-03 DOI:10.1145/3531231
Gina Sprint, Diane J Cook, Maureen Schmitter-Edgecombe, Lawrence B Holder
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引用次数: 0

摘要

新的技术模式为不露痕迹地收集人们的行为数据提供了前所未有的机会。虽然此类信息有很多用例,但我们要探讨的是它在预测多种临床评估分数方面的效用。由于临床评估通常被用作损伤和疾病(如轻度认知障碍(MCI))的筛查工具,因此将行为数据自动映射到评估分数有助于检测不同时期的健康和行为变化。在本文中,我们旨在从智能家居环境和定制数字记忆笔记本应用程序这两种模式中提取行为标记,并将其映射到与监测 MCI 发病和认知健康变化相关的十项临床评估中。基于智能家居的行为标记反映了每小时、每天和每周的活动模式,而基于应用程序的行为标记则反映了应用程序的使用情况以及从自由形式的日记条目中提取的写作内容/风格。我们介绍了融合这些多模态行为标记并利用联合预测的机器学习技术。我们使用三种回归算法和 14 名生活在智能家居环境中的 MCI 患者的数据对我们的方法进行了评估。我们观察到预测得分和地面实况评估得分之间存在中等到较大的相关性,每项临床评估的相关性从 r = 0.601 到 r = 0.871 不等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal Fusion of Smart Home and Text-based Behavior Markers for Clinical Assessment Prediction.

New modes of technology are offering unprecedented opportunities to unobtrusively collect data about people's behavior. While there are many use cases for such information, we explore its utility for predicting multiple clinical assessment scores. Because clinical assessments are typically used as screening tools for impairment and disease, such as mild cognitive impairment (MCI), automatically mapping behavioral data to assessment scores can help detect changes in health and behavior across time. In this paper, we aim to extract behavior markers from two modalities, a smart home environment and a custom digital memory notebook app, for mapping to ten clinical assessments that are relevant for monitoring MCI onset and changes in cognitive health. Smart home-based behavior markers reflect hourly, daily, and weekly activity patterns, while app-based behavior markers reflect app usage and writing content/style derived from free-form journal entries. We describe machine learning techniques for fusing these multimodal behavior markers and utilizing joint prediction. We evaluate our approach using three regression algorithms and data from 14 participants with MCI living in a smart home environment. We observed moderate to large correlations between predicted and ground-truth assessment scores, ranging from r = 0.601 to r = 0.871 for each clinical assessment.

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CiteScore
10.30
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