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Licensed Unlicensed Requires Authentication Published by De Gruyter April 17, 2020

Electrical stimulator with mechanomyography-based real-time monitoring, muscle fatigue detection, and safety shut-off: a pilot study

  • Jannatul Naeem , Nur Azah Hamzaid EMAIL logo , Amelia Wong Azman and Manfred Bijak

Abstract

Functional electrical stimulation (FES) has been used to produce force-related activities on the paralyzed muscle among spinal cord injury (SCI) individuals. Early muscle fatigue is an issue in all FES applications. If not properly monitored, overstimulation can occur, which can lead to muscle damage. A real-time mechanomyography (MMG)-based FES system was implemented on the quadriceps muscles of three individuals with SCI to generate an isometric force on both legs. Three threshold drop levels of MMG-root mean square (MMG-RMS) feature (thr50, thr60, and thr70; representing 50%, 60%, and 70% drop from initial MMG-RMS values, respectively) were used to terminate the stimulation session. The mean stimulation time increased when the MMG-RMS drop threshold increased (thr50: 22.7 s, thr60: 25.7 s, and thr70: 27.3 s), indicating longer sessions when lower performance drop was allowed. Moreover, at thr70, the torque dropped below 50% from the initial value in 14 trials, more than at thr50 and thr60. This is a clear indication of muscle fatigue detection using the MMG-RMS value. The stimulation time at thr70 was significantly longer (p = 0.013) than that at thr50. The results demonstrated that a real-time MMG-based FES monitoring system has the potential to prevent the onset of critical muscle fatigue in individuals with SCI in prolonged FES sessions.

Keywords: FES; KE; MMG; RMS; SCI

Acknowledgments

The authors acknowledge and appreciate all the SCI volunteers who participated in this study and colleagues who supported during the experiment.

  1. Research funding: The research was funded by the University of Malaya faculty Research Grant (GPF0688A-2018).

  2. Conflict of interest: The authors declare no conflict of interest.

  3. Informed consent: Each subject signed the consent form before starting the experiment procedure.

  4. Ethical approval: The research was approved by the University Malaya Medical Centre Ethics Committee [Approval No: 1003.14 (1)].

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Received: 2019-07-25
Accepted: 2020-01-07
Published Online: 2020-04-17
Published in Print: 2020-08-27

©2020 Walter de Gruyter GmbH, Berlin/Boston

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