Centre for Movement, Occupational and Rehabilitation Sciences, Oxford Brookes University, Oxford, UK.
Wellcome Centre for Integrative Neuroimaging (WIN), FMRIB, Nuffield Department of Clinical Neurosciences, University of Oxford, UK.
Clin Rehabil. 2021 Nov;35(11):1599-1610. doi: 10.1177/02692155211017360. Epub 2021 May 30.
To test the extent to which initial walking speed influences dual-task performance after walking intervention, hypothesising that slow walking speed affects automatic gait control, limiting executive resource availability.
A secondary analysis of a trial of dual-task (DT) and single-task (ST) walking interventions comparing those with (walking speed ⩾0.8 m s, = 21) and (walking speed <0.79 m s, = 24) capacity at baseline.
Community.
Adults six-months post stroke with walking impairment.
Twenty sessions of 30 minutes treadmill walking over 10 weeks with (DT) or without (ST) cognitive distraction. and groups were formed regardless of intervention received.
A two-minute walk with (DT) and without (ST) a cognitive distraction assessed walking. NIRS measured prefrontal cortex activation during treadmill walking with (DT) and without (ST) Stroop and planning tasks and an MRI sub-study used ankle-dorsiflexion to simulate walking.
ST walking improved in both groups (∆baseline: 8.9 ± 13.4 m, = 5.3±8.9 m, Group × time = < 0.151) but only the walkers improved DT walking (∆baseline: 10.4 ± 13.9 m, = 1.3 ± 7.7 m, Group × time = < 0.025). NIRS indicated increased ispilesional prefrontal cortex activation during DT walking following intervention ( = 0.021). MRI revealed greater DT cost activation for walkers, and increased resting state connectivity of contralesional M1 with cortical areas associated with conscious gait control at baseline. After the intervention, resting state connectivity between ipsilesional M1 and bilateral superior parietal lobe, involved in integrating sensory and motor signals, increased in the walkers compared with walkers.
In individual who walk slowly it may be difficult to improve dual-task walking ability. ISRCTN50586966.
测试初始步行速度对步行干预后双重任务表现的影响程度,假设慢步行速度会影响自动步态控制,限制执行资源的可用性。
对双重任务(DT)和单任务(ST)步行干预试验的二次分析,比较基线时具有 (步行速度 ⩾0.8 m s, = 21)和 (步行速度 <0.79 m s, = 24)能力的个体。
社区。
脑卒中后 6 个月有步行障碍的成年人。
10 周内进行 20 次 30 分钟跑步机步行,其中(DT)或不(ST)进行认知分心。无论接受何种干预,都会形成 和 组。
两分钟步行,同时进行(DT)和不进行(ST)认知分心,评估行走能力。近红外光谱(NIRS)测量在跑步机上行走时前额叶皮层的激活情况,同时进行(DT)和不进行(ST)Stroop 和规划任务,以及一项 MRI 子研究使用踝关节背屈来模拟行走。
两组的 ST 步行均有所改善(∆基线: 8.9 ± 13.4 m, = 5.3±8.9 m,组 × 时间 = < 0.151),但只有 组的 DT 步行有所改善(∆基线: 10.4 ± 13.9 m, = 1.3 ± 7.7 m,组 × 时间 = < 0.025)。NIRS 表明,干预后 DT 行走时对侧前额叶皮层的激活增加( = 0.021)。MRI 显示,在基线时,与意识性步态控制相关的对侧皮质运动区与皮质运动区的静息状态连接性增加,而 DT 成本激活增加。干预后,与 组相比,组的对侧 M1 与双侧顶叶上回之间的静息状态连接性增加,这些区域参与整合感觉和运动信号。
在步行速度较慢的个体中,可能难以提高双重任务步行能力。ISRCTN50586966。