4.7 Article

FLEXotendon Glove-III: Voice-Controlled Soft Robotic Hand Exoskeleton With Novel Fabrication Method and Admittance Grasping Control

Journal

IEEE-ASME TRANSACTIONS ON MECHATRONICS
Volume 27, Issue 5, Pages 3920-3931

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TMECH.2022.3148032

Keywords

Medical robots and systems; rehabilitation robotics; soft robot applications

Funding

  1. Shriners Hospitals for Children

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This article presents a novel voice-controlled soft robotic hand exoskeleton for hand assistance. The glove design uses high consistency rubber silicone and biomimetic tendon routing, providing a robust and optimal-fitting design with five-degree-of-freedom motion. The system includes a smartphone app-based voice user interface for intuitive control. Experimental results show that the system is effective for hand assistance and activity completion.
This article presents a voice-controlled soft robotic hand exoskeleton for hand assistance. Cervical spinal cord injury results in a disruption of the nerve signals, causing paralysis and limited upper extremity function. The impairment significantly limits the completion of activities of daily living (ADL) due to the importance of hand function. Recently, there has been an increase in hand exoskeleton studies to provide active assistance for effective ADL completion. However, the design, control, and user interface (UI) of the devices remain a challenging issue. This article proposes a novel fabrication method for the wearable glove using high consistency rubber silicone and biomimetic tendon routing. The developed glove provides a robust, deformable, and optimal-fitting design for an individual's hand with a weight of 131 g and five-degree-of-freedom motion for various ADLs. It provides a pinch force of 6.3 N and an object-level admittance controller was implemented for virtual grasping modalities. A smartphone app-based voice UI was developed to provide a truly portable and intuitive control system. Grasping experiments with a healthy participant were conducted to evaluate the system.

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