High-Dose Walking Booster Program Is Feasible for People After Stroke: A Phase II Randomized Trial.

IF 8.9 1区 医学 Q1 CLINICAL NEUROLOGY
Katharine Scrivener, Elisha Ball, Catherine Dean, Joanne Glinsky, Louise Ada, Petra Graham, Johannah Campbell, Karen Felton, Natasha Lannin
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Abstract

Background: Maintaining walking ability in the long term after a stroke is challenging. Furthermore, access to ongoing physiotherapy is limited. This trial determined the feasibility of a clinical trial of a high-dose walking booster program (HiWalk) and measured clinical outcomes.

Methods: A multisite, assessor-blinded pilot and feasibility randomized trial was conducted in Australia (June 2023 to July 2024). Participants had a stroke 6 months to 8 years prior and could walk unaided at 0.4 m/s to 1.0 m/s. The experimental group received HiWalk plus usual care, while the control group received usual care alone. HiWalk was group-based motor training to improve walking, 43 hours over 3 weeks. Feasibility outcomes included recruitment and retention. Clinical outcomes included walking speed (preferred and fast over 5 m, fast over 6 minutes), and self-efficacy at 1 and 6 months.

Results: Eighty-two individuals were screened, and 47 participated: age 58 (SD, 16), time poststroke 2.7 years (SD, 2.1), and baseline fast walking speed 0.9 m/s (SD, 0.4). Feasibility outcomes: the HiWalk trial was feasible in terms of recruitment (refusal rate 27%), retention at 1 month (98%), adherence (mean 91% [SD 13] attendance once commenced), safety (minor adverse events 0.4/wk), and measurement (98% of data collected at 1 month). Clinical outcomes: at month 1, there was a beneficial effect on a 30-point self-efficacy scale (MD, 3.0 [95% CI, 0.1-5.9]). However, despite a small positive mean effect of HiWalk on fast walking speed (MD, 0.05 m/s [95% CI, -0.09 to 0.19]), there were no other significant between group differences. Exploratory analysis suggests the effect on walking speed for those not undertaking rehabilitation was 0.24 m/s (95% CI, 0.06-0.43) more than for those who were.

Conclusions: The HiWalk booster program was a feasible way to deliver mobility training in the community after stroke. Benefits in clinical outcomes were found for the subgroup of participants no longer undertaking rehabilitation. Therefore, future research should target this subpopulation.

Registration: URL: https://www.anzctr.org.au; Unique identifier: ACTRN12623000316606p.

一项II期随机试验:高剂量步行增强计划对中风患者是可行的。
背景:中风后长期保持行走能力是具有挑战性的。此外,获得持续的物理治疗是有限的。该试验确定了高剂量步行增强程序(HiWalk)临床试验的可行性,并测量了临床结果。方法:于2023年6月至2024年7月在澳大利亚进行了一项多地点、评估盲的试点和可行性随机试验。参与者在6个月到8年前中风,可以以0.4米/秒到1.0米/秒的速度独立行走。实验组采用HiWalk +常规护理,对照组单独采用常规护理。HiWalk是一种以小组为基础的运动训练,以改善步行,在3周内进行43小时的训练。可行性结果包括招聘和保留。临床结果包括步行速度(首选和快超过5米,快超过6分钟),以及1个月和6个月的自我效能感。结果:筛选了82名个体,其中47名参与:年龄58岁(SD, 16),卒中后时间2.7年(SD, 2.1),基线快走速度0.9 m/s (SD, 0.4)。可行性结果:HiWalk试验在招募(拒绝率27%)、1个月的保留率(98%)、依从性(开始后平均91% [SD 13]出席率)、安全性(轻微不良事件0.4/周)和测量(1个月收集数据的98%)方面是可行的。临床结果:在第1个月,30分自我效能量表(MD, 3.0 [95% CI, 0.1-5.9])出现了有益的效果。然而,尽管HiWalk对快速步行速度有小的正平均影响(MD, 0.05 m/s [95% CI, -0.09至0.19]),但组间没有其他显著差异。探索性分析表明,与接受康复治疗的患者相比,未接受康复治疗的患者步行速度的影响为0.24 m/s (95% CI, 0.06-0.43)。结论:HiWalk增强计划是一种可行的方式来提供社区卒中后的活动能力训练。临床结果发现不再进行康复治疗的参与者亚组获益。因此,未来的研究应该针对这一亚群。注册:网址:https://www.anzctr.org.au;唯一标识符:ACTRN12623000316606p。
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来源期刊
Stroke
Stroke 医学-临床神经学
CiteScore
13.40
自引率
6.00%
发文量
2021
审稿时长
3 months
期刊介绍: Stroke is a monthly publication that collates reports of clinical and basic investigation of any aspect of the cerebral circulation and its diseases. The publication covers a wide range of disciplines including anesthesiology, critical care medicine, epidemiology, internal medicine, neurology, neuro-ophthalmology, neuropathology, neuropsychology, neurosurgery, nuclear medicine, nursing, radiology, rehabilitation, speech pathology, vascular physiology, and vascular surgery. The audience of Stroke includes neurologists, basic scientists, cardiologists, vascular surgeons, internists, interventionalists, neurosurgeons, nurses, and physiatrists. Stroke is indexed in Biological Abstracts, BIOSIS, CAB Abstracts, Chemical Abstracts, CINAHL, Current Contents, Embase, MEDLINE, and Science Citation Index Expanded.
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