Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Am J Hypertens. 2014 Jan;27(1):122-9. doi: 10.1093/ajh/hpt134. Epub 2013 Sep 14.
The HARMONY study was a randomized, controlled trial examining the efficacy of an 8-week mindfulness-based stress reduction (MBSR) program for blood pressure (BP) lowering among unmedicated stage 1 hypertensive participants.
Participants diagnosed with stage 1 hypertension based on ambulatory BP were randomized to either immediate treatment of MBSR for 8 weeks or wait-list control. Primary outcome analysis evaluated whether change in awake and 24-hour ambulatory BP from baseline to week 12 was significantly different between the 2 groups. A within-group before and after MBSR analysis was also performed.
The study enrolled 101 adults (38% male) with baseline average 24-hour ambulatory BP of 135±7.9/82±5.8mm Hg and daytime ambulatory BP of 140±7.7/87±6.3 mmHg. At week 12, the change from baseline in 24-hour ambulatory BP was 0.4±6.7/0.0±4.9mm Hg for the immediate intervention and 0.4±7.8/-0.4±4.6mm Hg for the wait-list control. There were no significant differences between intervention and wait-list control for all ambulatory BP parameters. The secondary within-group analysis found a small reduction in BP after MBSR compared with baseline, a finding limited to female subjects in a sex analysis.
MBSR did not lower ambulatory BP by a statistically or clinically significant amount in untreated, stage 1 hypertensive patients when compared with a wait-list control group. It leaves untested whether MBSR might be useful for lowering BP by improving adherence in treated hypertensive participants.
NCT00825526.
HARMONY 研究是一项随机对照试验,旨在检验为期 8 周的正念减压(MBSR)方案对未经药物治疗的 1 期高血压患者降低血压的疗效。
根据动态血压诊断为 1 期高血压的参与者被随机分为立即接受 MBSR 治疗 8 周或候补名单对照。主要结局分析评估了从基线到第 12 周,两组之间清醒和 24 小时动态血压的变化是否有显著差异。还对 MBSR 前后进行了组内分析。
该研究纳入了 101 名成年人(38%为男性),基线平均 24 小时动态血压为 135±7.9/82±5.8mmHg,日间动态血压为 140±7.7/87±6.3mmHg。在第 12 周,从基线到 24 小时动态血压的变化为即时干预组 0.4±6.7/0.0±4.9mmHg,候补名单对照组 0.4±7.8/-0.4±4.6mmHg。干预组与候补名单对照组之间所有动态血压参数均无显著差异。二次组内分析发现,与基线相比,MBSR 后血压略有下降,但在性别分析中仅限于女性。
与候补名单对照组相比,MBSR 并未使未经治疗的 1 期高血压患者的动态血压有统计学或临床意义的降低。这还没有测试 MBSR 是否可以通过提高治疗高血压患者的依从性来降低血压。
NCT00825526。