Division of General Internal Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Contemp Clin Trials. 2013 Sep;36(1):90-8. doi: 10.1016/j.cct.2013.06.002. Epub 2013 Jun 14.
A burgeoning literature suggests that exercise has a therapeutic benefit in persons with Parkinson disease (PD) and in animal models of PD, especially when animals exercise at high intensity. If exercise is to be prescribed as "first-line" or "add-on" therapy in patients with PD, we must demonstrate its efficacy and dose-response effects through testing phases similar to those used in the testing of pharmacologic agents. The SPARX Trial is a multicenter, randomized, controlled, single-blinded, Phase II study that we designed to test the feasibility of using high-intensity exercise to modify symptoms of PD and to simultaneously test the nonfutility of achieving a prespecified change in patients' motor scores on the Unified Parkinson Disease Rating Scale (UPDRS). The trial began in May 2102 and is in the process of screening, enrolling, and randomly assigning 126 patients with early-stage PD to 1 of 3 groups: usual care (wait-listed controls), moderate-intensity exercise (4 days/week at 60%-65% maximal heart rate [HRmax]), or high-intensity exercise (4 days/week at 80%-85% HRmax). At 6-month follow-up, the trial is randomly reassigning usual care participants to a moderate-intensity or high-intensity exercise group for the remaining 6 months. The goals of the Phase II trial are to determine if participants can exercise at moderate and high intensities; to determine if either exercise yields benefits consistent with meaningful clinical change (nonfutility); and to document safety and attrition. The advantage of using a non-futility approach allows us to efficiently determine if moderate- or high-intensity exercise warrants further large-scale investigation in PD.
不断增加的文献表明,运动对帕金森病(PD)患者和 PD 动物模型具有治疗益处,尤其是当动物进行高强度运动时。如果要将运动作为 PD 患者的“一线”或“附加”治疗方法,我们必须通过类似于药物测试阶段的测试来证明其疗效和剂量反应。SPARX 试验是一项多中心、随机、对照、单盲、II 期研究,旨在测试高强度运动是否可以改变 PD 症状,并同时测试在统一帕金森病评定量表(UPDRS)上达到预设患者运动评分变化的非无效性。该试验于 2012 年 5 月开始,目前正在筛选、招募和随机分配 126 名早期 PD 患者到以下 3 组之一:常规护理(候补对照组)、中等强度运动(每周 4 天,心率达到最大心率的 60%-65%[HRmax])或高强度运动(每周 4 天,心率达到 80%-85%HRmax)。在 6 个月随访时,试验将随机重新分配常规护理参与者到中等强度或高强度运动组,再进行接下来的 6 个月。II 期试验的目标是确定参与者是否可以进行中等强度和高强度运动;确定中等强度或高强度运动是否能带来一致的有意义的临床变化(非无效性);并记录安全性和失访情况。采用非无效性方法的优势在于,我们可以有效地确定中等强度或高强度运动是否值得在 PD 中进一步进行大规模研究。