Journal
DISABILITY AND REHABILITATION-ASSISTIVE TECHNOLOGY
Volume 16, Issue 3, Pages 241-250Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/17483107.2019.1668974
Keywords
Design requirements; user-centred design; focus group; electrical stimulation; neurorehabilitation; stroke; spinal cord injury
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The study aims to collect the views of future end-users and clinicians to optimize the development of novel FES-garments and strategies for commercialization. Identified themes provide guidelines for other rehabilitation and assistive technology developers to meet users' needs.
Purpose Functional electrical stimulation (FES), through repetitive training (FES-therapy) or continuous assistance (neuro-prosthesis), can restore motor function after paralysis due to spinal cord injury or stroke. With current technology, patients are often incapable of independently applying FES, thereby limiting its use. Novel FES-garments with embedded stimulation electrodes were developed in collaboration with Myant, Canada, to address this problem. The purpose of this study was to collect the views of future end-users to inform the refinement of the device design and to obtain insights on subsequent commercialization of this rehabilitation and assistive technology. Methods A qualitative study was undertaken to determine the needs of potential users (patients and clinicians; n = 19). Participant took part in interviews or focus groups after a presentation of the garments. An inductive content analysis was used to generate the themes from the data and identify data saturation. Results The identified themes and sub-themes were: (1) User Perspectives: users' characteristics (needs, limitations), expected benefits (beliefs), and anticipated problems (fears); (2) Device Design: technical features, usability, and disadvantages of the garment, cables, stimulator, software, and interface; (3) Acquisition Process: organizational procedures (acquisition and adoption steps); and (4) Business Model: financial and strategic aspects to facilitate commercialization and support users. Conclusions The insights obtained from end-users and clinicians provide guidelines to optimize the development of novel FES-garments, and strategies for bringing the device to the market. The themes identified can serve to inform other rehabilitation and assistive technology developers with processes and ideas on how to meet these groups' needs.
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