Department of Physical Therapy, University of Toronto, Canada.
BMC Neurol. 2010 Jun 9;10:40. doi: 10.1186/1471-2377-10-40.
Despite the cardiovascular etiology of stroke, exercise and risk factor modification programs akin to cardiac rehabilitation (CR) are not available. This study aimed to establish the feasibility of adapting a CR model for individuals with mild to moderate stroke disability. A secondary objective was to determine the program's effects on aerobic and walking capacity, and stroke risk factors.
A repeated measures design was used with a 3-month baseline period and 6-month adapted CR intervention (n = 43, mean +/- SD age 65 +/- 12 years, 30 +/- 28 months post stroke). Feasibility was determined by the number of participants who completed the study, occurrence of adverse events and frequency, duration and intensity of exercise performed. To determine effectiveness of the program, outcomes measured included aerobic capacity (VO2peak, ventilatory threshold), 6-Minute Walk Test (6MWT) distance, and risk factors. Descriptive statistics characterized the classes attended and number and intensity of exercise sessions. Paired t-tests, one-factor repeated measures analyses of variance contrasts and chi-square analyses were used to compare changes over time.
Two participants withdrew during the baseline period. Of the remaining 41 participants who commenced the program, 38 (93%) completed all aspects. No serious adverse effects occurred. Post-intervention, VO2peak improved relative to the stable baseline period (P = 0.046) and the increase in ventilatory threshold approached significance (P = 0.062).
CR is feasible after stroke and may be adapted to accommodate for those with a range of post-stroke disability. It is effective in increasing aerobic capacity. CR may be an untapped opportunity for stroke survivors to access programs of exercise and risk factor modification to lower future event risk.
ClinicalTrials.gov registration number: NCT01067495.
尽管中风的心血管病因,但针对轻度至中度中风残疾患者的运动和危险因素修改方案(类似于心脏康复)并不适用。本研究旨在建立适应心脏康复模式的可行性,以满足轻度至中度中风残疾患者的需求。次要目标是确定该方案对有氧运动和步行能力以及中风危险因素的影响。
本研究采用重复测量设计,包括 3 个月的基线期和 6 个月的适应性心脏康复干预期(n=43,平均年龄 65+/-12 岁,中风后 30+/-28 个月)。通过完成研究的参与者数量、不良事件的发生频率、运动的频率、持续时间和强度来确定可行性。为了确定该方案的有效性,测量的结果包括有氧能力(峰值摄氧量、通气阈值)、6 分钟步行测试(6MWT)距离以及危险因素。描述性统计分析了参加的课程数量以及运动课程的次数和强度。采用配对 t 检验、单因素重复测量方差分析对比和卡方检验比较随时间的变化。
在基线期有 2 名参与者退出。在开始该方案的 41 名剩余参与者中,有 38 名(93%)完成了所有方面。没有发生严重的不良事件。与稳定的基线期相比,干预后峰值摄氧量有所改善(P=0.046),通气阈值的增加也接近显著(P=0.062)。
中风后心脏康复是可行的,并且可以适应各种中风后残疾患者的需求。它能有效提高有氧运动能力。心脏康复可能是中风幸存者获得运动和危险因素修改方案的机会,以降低未来的发病风险。
ClinicalTrials.gov 注册号:NCT01067495。