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A randomized clinical trial of valerian fails to improve self-reported, polysomnographic, and actigraphic sleep in older women with insomnia.

机译:缬草的一项随机临床试验未能改善失眠老年妇女的自我报告睡眠,多导睡眠图和活动睡眠。

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OBJECTIVE: To test the effects of nightly valerian (Valeriana officinalis) extract to improve sleep of older women with insomnia. METHODS: Participants in this phase 2 randomized, double-blind, crossover controlled trial were 16 older women (mean age=69.4+/-8.1 years) with insomnia. Participants took 300 mg of concentrated valerian extract or placebo 30 min before bedtime for 2 weeks. Sleep was assessed in the laboratory by self-report and polysomnography (PSG) at baseline and again at the beginning and end of each treatment phase (total of nine nights in the laboratory) and at home by daily sleep logs and actigraphy. RESULTS: There were no statistically significant differences between valerian and placebo after a single dose or after 2 weeks of nightly dosing on any measure of sleep latency, wake after sleep onset (WASO), sleep efficiency, and self-rated sleep quality. In comparing each treatment to baseline in separate comparisons, WASO significantly increased (+17.7+/-25.6 min, p=.02) after 2 weeks of nightly valerian, but not after placebo (+6.8+/-26.4 min, NS). Side effects were minor and did not differ significantly between valerian and placebo. CONCLUSION: Valerian did not improve sleep in this sample of older women with insomnia. Findings from this study add to the scientific evidence that does not support use of valerian in the clinical management of insomnia.
机译:目的:测试夜间缬草提取物对失眠老年妇女睡眠的改善作用。方法:本项2期随机,双盲,交叉对照试验的参与者为16名失眠的老年妇女(平均年龄= 69.4 +/- 8.1岁)。参与者在就寝前30分钟服用300毫克浓缩缬草提取物或安慰剂,持续2周。在实验室中,通过自我报告和多导睡眠图(PSG)在基线以及每个治疗阶段的开始和结束时(实验室中总共9个晚上)再次评估睡眠,在家中通过每日睡眠记录和体动记录仪评估睡眠。结果:在任何剂量的睡眠潜伏期,入睡后醒来(WASO),睡眠效率和自我评价的睡眠质量的任何量度上,缬草和安慰剂之间在单剂量给药后或每晚给药2周后均无统计学差异。在单独比较中将每种治疗方案与基线进行比较时,夜间缬草治疗2周后WASO显着增加(+17.7 +/- 25.6 min,p = .02),而安慰剂治疗后则无统计学意义(+6.8 +/- 26.4 min,NS)。缬草和安慰剂之间的副作用很小,无明显差异。结论:缬草没有改善失眠的老年妇女的睡眠。这项研究的发现增加了不支持在失眠临床治疗中使用缬草的科学证据。

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