Kato Daisuke, Hirano Satoshi, Imoto Daisuke, Ii Takuma, Matsuura Daisuke, Ishihara Takuma, Otaka Yohei
Department of Rehabilitation, Fujita Health University Hospital, 1-98 Dengakugakubo, Kutsukake-Cho, Toyoake, Aichi, 470-1192, Japan.
Department of Rehabilitation Medicine, School of Medicine, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-Cho, Toyoake, Aichi, 470-1192, Japan.
Pilot Feasibility Stud. 2025 Aug 29;11(1):116. doi: 10.1186/s40814-025-01694-6.
Robot-assisted gait training (RAGT) has proven effective in addressing gait disorders in patients with stroke. However, its efficacy in patients with acute stroke has not yet been demonstrated. This pilot study is designed to evaluate the following: (1) feasibility of conducting a randomized controlled trial on RAGT for enhancing gait postacute stroke and (2) to obtain preliminary estimates regarding the potential efficacy of RAGT for achieving gait independence during the acute phase.
We will conduct an assessor-blinded, single-center, randomized controlled pilot trial involving 32 patients with acute stroke who are unable to walk. Participants will be randomly assigned to either the RAGT or the conventional gait training (CGT) groups. Each participant will receive 180 min of daily rehabilitation, including 60 min dedicated to gait training. The RAGT group will receive 40 min of RAGT and 20 min of CGT, while the CGT group will engage in 60 min of CGT. Interventions will continue for up to 8 weeks, or until participants achieve gait independence, as indicated by a Functional Ambulation Category score of ≥ 3. Feasibility outcomes will include recruitment, enrollment, protocol adherence, and retention rates. The primary clinical outcome will be the incidence of achieving gait independence during the intervention period. Secondary clinical outcomes will include gait performance measures, assessments of physical function and activity, and intervention dose. Adverse events associated with RAGT and CGT will also be documented to evaluate the safety of both interventions.
Implementing RAGT during the acute phase of stroke may facilitate earlier attainment of gait independence compared to CGT. We aim to provide valuable insights into the feasibility of the proposed study design and generate preliminary data on the potential effects of RAGT on gait independence in the acute phase of stroke, providing a framework for future larger-scale trials.
This clinical trial was registered with the Japan Clinical Trials Registry (jRCT) on 19 June 2023 (registration number: jRCTs042230040). The study protocol was initially registered as version 1.0 and has since undergone minor amendments-currently on version 4.0. This protocol was written based on the latest version (ver. 4.0) registered with jRCT.
事实证明,机器人辅助步态训练(RAGT)在治疗中风患者的步态障碍方面是有效的。然而,其在急性中风患者中的疗效尚未得到证实。这项初步研究旨在评估以下内容:(1)针对急性中风后改善步态开展RAGT随机对照试验的可行性,以及(2)获得关于RAGT在急性期实现步态独立的潜在疗效的初步估计。
我们将开展一项评估者盲法、单中心、随机对照的初步试验,纳入32例无法行走的急性中风患者。参与者将被随机分配到RAGT组或传统步态训练(CGT)组。每位参与者每天将接受180分钟的康复治疗,其中包括60分钟专门用于步态训练。RAGT组将接受40分钟的RAGT和20分钟的CGT,而CGT组将进行60分钟的CGT。干预将持续长达8周,或直至参与者实现步态独立,即功能性步行分类评分≥3。可行性结果将包括招募、入组、方案依从性和保留率。主要临床结果将是干预期间实现步态独立的发生率。次要临床结果将包括步态性能指标、身体功能和活动评估以及干预剂量。还将记录与RAGT和CGT相关的不良事件,以评估两种干预措施的安全性。
与CGT相比,在中风急性期实施RAGT可能有助于更早实现步态独立。我们旨在为拟议的研究设计的可行性提供有价值的见解,并生成关于RAGT对中风急性期步态独立潜在影响的初步数据,为未来更大规模的试验提供框架。
本临床试验于2023年6月19日在日本临床试验注册中心(jRCT)注册(注册号:jRCTs042230040)。研究方案最初注册为版本1.0,此后进行了小幅修订,目前为版本4.0。本方案是根据在jRCT注册的最新版本(版本4.0)编写的。