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家庭虚拟康复系统(HoVRS)的开发,旨在远程提供高强度和定制化的上肢训练。

Development of the Home based Virtual Rehabilitation System (HoVRS) to remotely deliver an intense and customized upper extremity training.

机构信息

Department of Rehabilitation & Movement Sciences, School of Health Professions, Rutgers Biomedical and Health Sciences, Newark, NJ, USA.

Department of Biomedical Engineering, New Jersey Institute of Technology, Newark, NJ, 70102, USA.

出版信息

J Neuroeng Rehabil. 2020 Nov 23;17(1):155. doi: 10.1186/s12984-020-00789-w.

Abstract

BACKGROUND

After stroke, sustained hand rehabilitation training is required for continuous improvement and maintenance of distal function.

METHODS

In this paper, we present a system designed and implemented in our lab: the Home based Virtual Rehabilitation System (HoVRS). Fifteen subjects with chronic stroke were recruited to test the feasibility of the system as well as to refine the design and training protocol to prepare for a future efficacy study. HoVRS was placed in subjects' homes, and subjects were asked to use the system at least 15 min every weekday for 3 months (12 weeks) with limited technical support and remote clinical monitoring.

RESULTS

All subjects completed the study without any adverse events. Subjects on average spent 13.5 h using the system. Clinical and kinematic data were collected pre and post study in the subject's home. Subjects demonstrated a mean increase of 5.2 (SEM = 0.69) on the Upper Extremity Fugl-Meyer Assessment (UEFMA). They also demonstrated improvements in six measurements of hand kinematics. In addition, a combination of these kinematic measures was able to predict a substantial portion of the variability in the subjects' UEFMA score.

CONCLUSION

Persons with chronic stroke were able to use the system safely and productively with minimal supervision resulting in measurable improvements in upper extremity function.

摘要

背景

中风后,需要持续进行手部康复训练,以不断提高和维持手部远端功能。

方法

本文介绍了我们实验室设计和实现的系统:基于家庭的虚拟康复系统(HoVRS)。招募了 15 名慢性中风患者来测试该系统的可行性,并进一步完善设计和训练方案,为未来的疗效研究做准备。HoVRS 被放置在患者家中,要求患者在 3 个月(12 周)的每个工作日至少使用系统 15 分钟,同时提供有限的技术支持和远程临床监测。

结果

所有患者均顺利完成研究,未发生任何不良事件。患者平均使用系统 13.5 小时。在患者家中进行研究前后收集临床和运动学数据。患者上肢 Fugl-Meyer 评估(UEFMA)平均增加 5.2(SEM=0.69)。手部运动学的 6 项测量也得到了改善。此外,这些运动学测量的组合能够预测患者 UEFMA 评分的大部分变化。

结论

慢性中风患者能够在最少的监督下安全有效地使用该系统,从而使上肢功能得到可衡量的改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/7685660/f931c91cee18/12984_2020_789_Fig1_HTML.jpg

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