4.6 Article

Exoskeleton-Assisted Anthropomorphic Movement Training (EAMT) for Poststroke Upper Limb Rehabilitation: A Pilot Randomized Controlled Trial

Journal

ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
Volume 102, Issue 11, Pages 2074-2082

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.apmr.2021.06.001

Keywords

Rehabilitation; Robtics; Stroke; Upper extremity

Funding

  1. National Natural Science Foundation of China [U 1913601, 91648203]

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The feasibility of exoskeleton-assisted anthropomorphic movement training (EAMT) was investigated in a pilot randomized controlled trial involving 20 participants with subacute stroke. EAMT therapy was found to be feasible, acceptable, and safe, with significant improvements in FMA-UE, MBI, and kinematic metrics in favor of the EAMT group. Fully powered randomized controlled trials are needed to confirm these results and explore the underlying mechanisms of EAMT therapy.
Objective: To investigate the feasibility of exoskeleton-assisted anthropomorphic movement training (EAMT) and its effects on upper extremity motor impairment, function, and kinematics after stroke. Design: A single-blind pilot randomized controlled trial. Setting: Stroke rehabilitation inpatient unit. Participants: Participants with a hemiplegia (N=20) due to a first-ever, unilateral, subacute stroke who had a score of 8-47 on the Fugl-Meyer Assessment for Upper Extremity (FMA-UE). Interventions: The exoskeleton group received EAMT therapy that provided task-specific training under anthropomorphic trajectories and pos-tures. The control group received conventional upper limb therapy. For both groups, therapy was delivered at the same intensity, frequency, and duration: 45 minutes daily, 5 days per week, for 4 weeks. Main Outcome Measures: Primary outcome: feasibility analysis. Secondary outcomes: FMA-UE, Action Research Arm Test (ARAT), modified Barthel Index (MBI), and kinematic metrics during exoskeleton therapy. Results: Twenty participants with subacute stroke were recruited and completed all therapy sessions. EAMT therapy was feasible and acceptable for the participants. The recruitment rate, retention rate, and number of therapists required for EAMT therapy were accept-able compared with other robotic trials. EAMT was determined to be safe, as no adverse event occurred except tolerable muscle fatigue in 2 participants. There were significant between-group differences in the change scores of FMA-UE (difference, 4.30 points; P=.04) and MBI (difference, 8.70 points; P=.03) in favor of EAMT therapy. No significant between-group difference was demon-strated for the change scores of ARAT (P=.18). Participants receiving EAMT showed significant improvements in kinematic metrics after treatment (P<.01). Conclusions: Our results indicate that EAMT is a feasible approach and may improve upper extremity motor impairment, activities of daily living, and kinematics after stroke. However, fully powered randomized controlled trials are warranted to confirm the results of this pilot study and explore the underlying mechanisms by which EAMT therapy might work. (C) 2021 The American Congress of Rehabilitation Medicine. Published by Elsevier Inc. All rights reserved.

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