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Characterization of the Force Production Capabilities of Paralyzed Trunk Muscles Activated With Functional Neuromuscular Stimulation in Individuals With Spinal Cord Injury. | LitMetric

Unlabelled: Paralysis of the trunk results in seated instability leading to difficulties performing activities of daily living. Functional neuromuscular stimulation (FNS) combined with control systems have the potential to restore some dynamic functions of the trunk. However, design of multi-joint, multi-muscle control systems requires characterization of the stimulation-driven muscles responsible for movement.

Objective: This study characterizes the input-output properties of paralyzed trunk muscles activated by FNS, and explores co-activation of muscles.

Methods: Four participants with various spinal cord injuries (C7 AIS-B, T4 AIS-B, T5 AIS-A, C5 AIS-C) were constrained so lumbar forces were transmitted to a load cell while an implanted neuroprosthesis activated otherwise paralyzed hip and paraspinal muscles. Isometric force recruitment curves in the nominal seated position were generated by inputting the level of stimulation (pulse width modulation) while measuring the resulting muscle force. Two participants returned for a second experiment where muscles were co-activated to determine if their actions combined linearly.

Results: Recruitment curves of most trunk and hip muscles fit sigmoid shaped curves with a regression coefficient above 0.75, and co-activation of the muscles combined linearly across the hip and lumbar joint. Subject specific perturbation plots showed one subject is capable of resisting up to a 300N perturbation anteriorly and 125N laterally; with some subjects falling considerably below these values.

Conclusion: Development of a trunk stability control system can use sigmoid recruitment dynamics and assume muscle forces combine linearly.

Significance: This study informs future designs of multi-muscle, and multi-dimensional FNS systems to maintain seated posture and stability.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131402PMC
http://dx.doi.org/10.1109/TBME.2020.3039404DOI Listing

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