Randomized, crossover clinical trial on the safety, feasibility, and usability of the ABLE exoskeleton: A comparative study with knee-ankle-foot orthoses.

IF 2.9 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-05-27 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0318039
Antonio Rodríguez-Fernández, Joan Lobo-Prat, Mariona Tolrà-Campanyà, Florentina Pérez-Cañabate, Josep M Font-Llagunes, Lluis Guirao-Cano
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Abstract

Wearable exoskeletons are emerging as a new tool for gait training. However, comparisons between exoskeletons and conventional orthoses in terms of safety and feasibility are scarce. This study assessed the safety, feasibility, usability, and learning process of using the ABLE Exoskeleton in people with spinal cord injury (SCI) while comparing it with knee-ankle-foot orthoses (KAFOs). In this randomized, crossover clinical trial, 10 patients with chronic complete SCI (T4-T12) conducted a 10-session training and assessment protocol with each device: KAFOs and the ABLE Exoskeleton. Outcomes on safety (adverse events), and feasibility and usability (level of assistance, donning/doffing, therapy activities) were recorded for both devices. Evaluation sessions included standard clinical tests (Timed Up and Go, 10-Meter Walk Test, and 6-Minute Walk Test) to assess gait performance. The therapy metrics (number of steps, distance, gait speed, and standing and walking time) were recorded at each session for the robotic device. Participants quickly learned how to use the ABLE Exoskeleton, showing improvements in all therapy metrics (p<0.05) and the 6-Minute Walk Test (p<0.05). Participants reported less adverse events with the robotic device than KAFOs (17 and 31, respectively). Total donning and doffing time was 43 s faster with the robotic device using comparable levels of assistance. The time to complete the therapy activities was very similar between devices. Overall, participants needed 1 to 4 training sessions to perform essential therapy activities (sit/stand transitions, walking 10 meters, turning around) with both devices using minimum assistance or less. The results of this study show that it is feasible and safe for people with motor complete paraplegia due to SCI (T4-T12) to use the ABLE Exoskeleton for gait training in a rehabilitation hospital setting. The ABLE Exoskeleton proved to be as practical and easy to use as conventional orthoses, with fewer AEs reported when using the exoskeleton versus the KAFOs.

ABLE外骨骼的安全性、可行性和可用性的随机交叉临床试验:与膝-踝-足矫形器的比较研究。
可穿戴外骨骼正在成为步态训练的新工具。然而,外骨骼矫形器与传统矫形器在安全性和可行性方面的比较很少。本研究评估了在脊髓损伤(SCI)患者中使用ABLE Exoskeleton的安全性、可行性、可用性和学习过程,并将其与膝-踝-足矫形器(KAFOs)进行了比较。在这项随机交叉临床试验中,10名慢性完全性脊髓损伤(T4-T12)患者分别使用KAFOs和ABLE Exoskeleton进行了10次训练和评估。记录两种器械的安全性(不良事件)、可行性和可用性(辅助水平、穿戴/脱下、治疗活动)的结果。评估环节包括标准的临床测试(计时起来和走,10米步行测试和6分钟步行测试)来评估步态表现。在机器人装置的每个疗程中记录治疗指标(步数,距离,步态速度,站立和行走时间)。参与者很快学会了如何使用ABLE Exoskeleton,显示出所有治疗指标的改善
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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