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使用自适应设备对有行走障碍的多发性硬化症患者进行高强度间歇训练方案的可行性和初步疗效的临床研究结果。

Results of a feasibility and initial efficacy clinical trial of a high-intensity interval training program using adaptive equipment in persons with multiple sclerosis who have walking disability.

机构信息

Department of Kinesiology, Health Promotion, and Recreation, University of North Texas, 1155 Union Circle #310769, Denton, TX 76203, USA; Department of Management, Policy, and Community Health, University of Texas Health Science Center at Houston, 1200 Pressler Street, Houston, TX, 77030, USA.

Department of Kinesiology and Nutrition, University of Illinois Chicago, 1919 W. Taylor St., 506H AHSB Chicago, IL, 60612, USA.

出版信息

Mult Scler Relat Disord. 2024 Jul;87:105695. doi: 10.1016/j.msard.2024.105695. Epub 2024 May 24.

DOI:10.1016/j.msard.2024.105695
PMID:38820697
Abstract

BACKGROUND

High intensity interval training (HIIT) has been identified as potential stimulus for eliciting health-promoting physical activity in an efficient manner among persons with multiple sclerosis (MS). The current study aimed to examine the feasibility and initial efficacy of a 12-week HIIT program using a recumbent stepper (RSTEP) in persons with MS who have walking disability. Feasibility outcomes of interest included process (i.e., recruitment, adherence, and retention rates), resource (i.e., time and monetary costs), management (i.e., data management and safety reporting assessment), and science (i.e., safety, burden, and treatment effect assessment). We hypothesized that 12-weeks of HIIT will be feasible via meeting a priori benchmarks in process, resource, management, and scientific outcomes. The efficacy outcomes of interest included changes in aerobic fitness, physical activity, walking, upper arm function, cognition, fatigue, and depressive symptoms. We hypothesized that 12 weeks of HIIT would result in improvements in aerobic capacity, walking, upper arm function, cognition, fatigue, and depression.

METHODS

A pre-post clinical trial design was applied. Participants (N = 16) were recruited and enrolled in the 12-week RSTEP HIIT program who met the following inclusion criteria: age ≥18 years, self-reported diagnosis of MS, Patient Determined Disability Steps scale score 3.0-7.0, relapse free in past 30 days, willing to visit a University Laboratory for study protocol, asymptomatic status for maximal exercise testing, physician approval, and a self-reported ability to speak, read, and understand English. Measures of efficacy outcomes of interest included Six Minute Walk Test (6MW), Timed 25 Foot Walk Test (T25FW), the Brief International Cognitive Assessment in MS (BICAMS), 9-hole peg test (9-HPT), Expanded Disability Status Scale (EDSS), Fatigue Severity Survey (FSS), Hospital Anxiety and Depression Scale (HADS), Godin Leisure Time Exercise Questionnaire (GLTEQ), Multiple Sclerosis Walking Scale-12 (MSWS-12). Participants completed a graded maximal exercise test for measuring aerobic fitness (VO) and prescription of exercise throughout the intervention. All outcomes were measured at baseline, mid-point (6-weeks), and post-intervention (12-weeks). The intervention involved 12 weeks of supervised, individualized HIIT sessions two times per week using RSTEP. The individual HIIT sessions included 10 cycles of 60 s intervals at the work rate associated with 90 % VO followed by 60 s of active recovery intervals, totaling 20 minutes plus 5-minute warm-up and cool-down periods. Process, resources, management, and scientific feasibility outcomes were examined using descriptive statistics, percentage, and frequency analyses. The efficacy of the intervention was assessed using a 1-factor (Time), repeated measure analysis of variance to identify significant changes over time.

RESULTS

Fourteen of 16 participants were retained throughout the full study period and adherence with prescribed exercise sessions was 97 %. Twenty-three staff were comprehensively trained across two sites. There was only one adverse event reported that did not impact participation in the study and overall mean satisfaction rating with the program among participants was 4.7/5. There were statistically significant changes in cognitive processing speed (p = 0.002), GLTEQ (p = 0.005), and MSWS-12 (p = 0.04), but not the other outcomes of fitness, arm function, and walking. Of note, there were large effect sizes noted for peak power output (d = 1.10) and FSS (d = 1.05) despite the lack of statistically significant changes CONCLUSION: Feasibility of a 12-week individualized RSTEP HIIT program was established and participants significantly improved on measures of cognition, physical activity, and walking.

摘要

背景

高强度间歇训练(HIIT)已被确定为在患有多发性硬化症(MS)的人群中以高效的方式产生促进健康的身体活动的潜在刺激。本研究旨在检验使用卧式踏步器(RSTEP)进行 12 周 HIIT 计划在有行走障碍的 MS 患者中的可行性和初步疗效。感兴趣的可行性结果包括过程(即招募、依从性和保留率)、资源(即时间和金钱成本)、管理(即数据管理和安全报告评估)和科学(即安全性、负担和治疗效果评估)。我们假设,通过在过程、资源、管理和科学结果方面达到事先设定的基准,12 周的 HIIT 将是可行的。感兴趣的疗效结果包括有氧健身、身体活动、行走、上臂功能、认知、疲劳和抑郁症状的变化。我们假设 12 周的 HIIT 将导致有氧能力、行走、上臂功能、认知、疲劳和抑郁的改善。

方法

采用前后临床试验设计。符合以下纳入标准的参与者(N=16)被招募并纳入 12 周的 RSTEP HIIT 计划:年龄≥18 岁、自我报告的 MS 诊断、患者确定的残疾步骤量表评分 3.0-7.0、过去 30 天内无复发、愿意到大学实验室进行研究方案、最大运动测试无症状状态、医生批准、以及能够说、读和理解英语的自我报告能力。感兴趣的疗效结果的测量包括 6 分钟步行测试(6MW)、25 英尺定时步行测试(T25FW)、多发性硬化症简明认知评估量表(BICAMS)、9 孔钉测试(9-HPT)、扩展残疾状况量表(EDSS)、疲劳严重程度调查(FSS)、医院焦虑和抑郁量表(HADS)、戈丁休闲时间运动问卷(GLTEQ)、多发性硬化症行走量表-12(MSWS-12)。参与者完成了一项分级最大运动测试,以测量有氧健身(VO)并在整个干预过程中开具运动处方。所有结果均在基线、中点(6 周)和干预后(12 周)进行测量。干预包括 12 周、每周两次的监督、个体化 HIIT 课程,使用 RSTEP 进行。每个 HIIT 课程包括 10 个 60 秒的间隔,工作率与 90%VO 相关,随后是 60 秒的主动恢复期,总时长 20 分钟,加上 5 分钟的热身和冷却期。使用描述性统计、百分比和频率分析来检查过程、资源、管理和科学可行性结果。使用 1 因素(时间)、重复测量方差分析评估干预的疗效,以确定随时间的显著变化。

结果

16 名参与者中有 14 名在整个研究期间保留下来,与规定的运动课程的依从性为 97%。两个地点共培训了 23 名工作人员。仅报告了一起不良事件,不影响参与研究,参与者对该计划的总体满意度平均评分为 4.7/5。认知处理速度(p=0.002)、GLTEQ(p=0.005)和 MSWS-12(p=0.04)的变化具有统计学意义,但健身、手臂功能和行走的其他结果没有变化。值得注意的是,尽管没有统计学上的显著变化,但峰值功率输出(d=1.10)和 FSS(d=1.05)的效果量很大。

结论

建立了 12 周个体化 RSTEP HIIT 计划的可行性,参与者在认知、身体活动和行走方面的测量有显著改善。

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