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卒中后无监督机器人辅助康复:可行性、对治疗剂量的影响和用户体验。

Unsupervised robot-assisted rehabilitation after stroke: feasibility, effect on therapy dose, and user experience.

机构信息

Rehabilitation Engineering Laboratory, Department of Health Sciences and Technology, ETH Zurich, Switzerland.

Clinica Hildebrand Centro di riabilitazione Brissago, Brissago, Switzerland.

出版信息

J Neuroeng Rehabil. 2024 Apr 9;21(1):52. doi: 10.1186/s12984-024-01347-4.

Abstract

BACKGROUND

Unsupervised robot-assisted rehabilitation is a promising approach to increase the dose of therapy after stroke, which may help promote sensorimotor recovery without requiring significant additional resources and manpower. However, the unsupervised use of robotic technologies is not yet a standard, as rehabilitation robots often show low usability or are considered unsafe to be used by patients independently. In this paper we explore the feasibility of unsupervised therapy with an upper limb rehabilitation robot in a clinical setting, evaluate the effect on the overall therapy dose, and assess user experience during unsupervised use of the robot and its usability.

METHODS

Subacute stroke patients underwent a four-week protocol composed of daily 45 min-sessions of robot-assisted therapy. The first week consisted of supervised therapy, where a therapist explained how to interact with the device. The second week was minimally supervised, i.e., the therapist was present but intervened only if needed. After this phase, if participants learnt how to use the device, they proceeded to two weeks of fully unsupervised training. Feasibility, dose of robot-assisted therapy achieved during unsupervised use, user experience, and usability of the device were evaluated. Questionnaires to evaluate usability and user experience were performed after the minimally supervised week and at the end of the study, to evaluate the impact of therapists' absence.

RESULTS

Unsupervised robot-assisted therapy was found to be feasible, as 12 out of the 13 recruited participants could progress to unsupervised training. During the two weeks of unsupervised therapy participants on average performed an additional 360 min of robot-assisted rehabilitation. Participants were satisfied with the device usability (mean System Usability Scale scores > 79), and no adverse events or device deficiencies occurred.

CONCLUSIONS

We demonstrated that unsupervised robot-assisted therapy in a clinical setting with an actuated device for the upper limb was feasible and can lead to a meaningful increase in therapy dose. These results support the application of unsupervised robot-assisted therapy as a complement to usual care in clinical settings and pave the way to its application in home settings.

TRIAL REGISTRATION

Registered on 13.05.2020 on clinicaltrials.gov (NCT04388891).

摘要

背景

无监督机器人辅助康复是增加中风后治疗剂量的一种很有前途的方法,这可能有助于促进感觉运动康复,而无需大量额外的资源和人力。然而,机器人技术的无监督使用还不是一种标准,因为康复机器人的可用性通常较低,或者被认为不安全,不能让患者独立使用。在本文中,我们探讨了在临床环境中使用上肢康复机器人进行无监督治疗的可行性,评估了对整体治疗剂量的影响,并评估了患者在使用机器人时的用户体验及其可用性。

方法

亚急性中风患者接受了为期四周的方案,包括每天 45 分钟的机器人辅助治疗。第一周为监督治疗,治疗师在此期间解释如何与设备互动。第二周为最小监督,即治疗师在场,但仅在需要时进行干预。在这个阶段之后,如果参与者学会了如何使用设备,他们就可以进行两周的完全无监督训练。评估了可行性、无监督使用期间机器人辅助治疗的剂量、用户体验和设备的可用性。在最小监督周后和研究结束时进行了评估可用性和用户体验的问卷,以评估治疗师缺席的影响。

结果

无监督机器人辅助治疗被证明是可行的,因为 13 名招募的参与者中有 12 名可以进行无监督训练。在两周的无监督治疗期间,参与者平均增加了 360 分钟的机器人辅助康复。参与者对设备的可用性感到满意(平均系统可用性量表评分>79),没有发生不良事件或设备缺陷。

结论

我们证明了在临床环境中使用带驱动器的上肢无监督机器人辅助治疗是可行的,可以显著增加治疗剂量。这些结果支持在临床环境中应用无监督机器人辅助治疗作为常规护理的补充,并为其在家中应用铺平了道路。

试验注册

于 2020 年 5 月 13 日在 clinicaltrials.gov 上注册(NCT04388891)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d97b/11005116/f541f87bea44/12984_2024_1347_Fig1_HTML.jpg

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