Effect of Functional Electrical Stimulation in Convalescent Stroke Patients: A Multicenter, Randomized Controlled Trial

Author:

Matsumoto Shuji12,Shimodozono Megumi3,Noma Tomokazu4,Miyara Kodai5,Onoda Tetsuya6,Ijichi Rina7,Shigematsu Takashi8,Satone Akira9,Okuma Hidenobu10,Seto Makiko11,Taketsuna Masanori12,Kaneda Hideaki12,Matsuo Miyuki12,Kojima Shinsuke12ORCID,

Affiliation:

1. Center of Medical Education, Faculty of Health Sciences, Ryotokuji University, Chiba 279-8567, Japan

2. Department of Rehabilitation and Physical Medicine, Mito Clinical Education and Training Center, University of Tsukuba Hospital, Mito 310-0015, Japan

3. Department of Rehabilitation and Physical Medicine, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan

4. Department of Rehabilitation, Faculty of Health Science, Nihon Fukushi University, Aichi 470-3295, Japan

5. Department of Rehabilitation, Kagoshima University Hospital, Kagoshima 890-0075, Japan

6. Department of Rehabilitation, Kirishima Medical Center, Kagoshima 899-5112, Japan

7. Department of Rehabilitation, Kirishima Sugiyasu Hospital, Kagoshima 899-4201, Japan

8. Department of Rehabilitation, Hamamatsu City Rehabilitation Hospital, Shizuoka 433-8511, Japan

9. Department of Rehabilitation, Tokachi Rehabilitation Center, Hokkaido 080-0835, Japan

10. Department of Rehabilitation, Kumamoto Takumadai Rehabilitation Hospital, Kumamoto 862-0924, Japan

11. Department of Rehabilitation, Nagasaki Kita Hospital, Nagasaki 851-2103, Japan

12. Translational Research Center for Medical Innovation, Kobe 650-0047, Japan

Abstract

Background: We evaluated whether the Walkaide® device could effectively improve walking ability and lower extremity function in post-stroke patients with foot drop. Patients aged 20–85 years with an initial stroke within ≤6 months and a functional ambulation classification score of 3 or 4 were eligible. Materials and Methods: Patients were randomly allocated to the functional electrical stimulation (FES) or control group at a 1:1 ratio. A 40 min training program using Walkaide was additionally performed by the FES group five times per week for 8 weeks. The control group received the 40 min training program without FES. Results: A total of 203 patients were allocated to the FES (n = 102) or control (n = 101) groups. Patients who did not receive the intervention or whose data were unavailable were excluded. Finally, the primary outcome data of 184 patients (n = 92 in each group) were analyzed. The mean change in the maximum distance during the 6-MWT (primary outcome) was 68.37 ± 62.42 m and 57.50 ± 68.17 m in the FES and control groups (difference: 10.86 m; 95% confidence interval: −8.26 to 29.98, p = 0.26), respectively. Conclusions: In Japanese post-stroke patients with foot drop, FES did not significantly improve the 6 min walk distance during the convalescent phase. The trial was registered at UMIN000020604.

Funder

Teijin Pharma Ltd.

Publisher

MDPI AG

Subject

General Medicine

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