Development of a knee joint assist suit with a velocity-based mechanical safety device: Control method and experiments

被引:0
|
作者
Ikeda, Keisuke [1 ]
Kaneda, Tsubasa [1 ]
Kai, Yoshihiro [1 ]
Sugawara, Kenichi [2 ]
Tanioka, Tetsuya [3 ]
Tomizuka, Masayoshi [4 ]
Zhao, Yueren [5 ]
Takase, Kensaku [6 ]
Dino, Michael Joseph S. [7 ]
机构
[1] Tokai Univ, Dept Mech Engn, Hiratsuka, Kanagawa, Japan
[2] Kanagawa Univ Human Serv, Dept Rehabil, Yokosuka, Kanagawa, Japan
[3] Tokushima Univ, Inst Biomed Sci, Dept Nursing, Tokushima, Japan
[4] Univ Calif Berkeley, Dept Mech Engn, Berkeley, CA 94720 USA
[5] Fujita Hlth Univ, Dept Psychiat, Toyoake, Aichi, Japan
[6] Tokushima Prefectural Cent Hosp, Dept Acute Stroke Rehabil, Tokushima, Japan
[7] Our Lady Fatima Univ, Res Dev & Innovat Ctr, Valenzuela, Philippines
来源
ENFERMERIA CLINICA | 2020年 / 30卷
关键词
Robot; Rehabilitation; Assist suit; Control method; OSTEOARTHRITIS; HIP;
D O I
10.1016/j.enfcli.2019.12.006
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
The aim of this study is to examine the proposed control method of the assist suit with a Velocity-Based Mechanical Safety Device (VBMSD) for patients with difficulty moving their lower legs by themselves. The proposed control method for the assist suit assists the patients as if the patients move their knee joint under zero gravity. A physical simulation model is used to examine whether the gravitational torque of the subject's lower leg and foot was canceled by the torque generated by the assist suit. Experimental results indicated that the gravitational torque of the subject's lower leg and foot is canceled by the torque generated by the assist suit. The control of the assist suit was not adversely influenced by the VBMSD. That is, the VBMSD did not prevent the control of the assist suit. The proposed control method makes the assist suit assist the patient in moving his/her knee joint in a zero gravity-like environment. However, a weight of 3 kg was used instead of an actual patient in the experiment. Experiments with actual patients should be conducted to verify the effectiveness of the proposed control method in clinical use. Furthermore, it will be necessary to take into consideration the patients' general conditions and symptoms. (C) 2019 Elsevier Espana, S.L.U. All rights reserved.
引用
收藏
页码:23 / 26
页数:4
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