School of Medicine, Universidad de los Andes, Carrera 7 No 116-05, Of 413, 110111, Bogotá, Colombia.
Department of Neurology, Hospital Universitario Fundación Santa Fe de Bogotá, Bogotá, Colombia.
Sci Rep. 2024 Apr 5;14(1):8062. doi: 10.1038/s41598-024-58661-z.
In this randomised, placebo-controlled trial, adults with impaired sleep (Pittsburgh Sleep Quality Index ≥ 5) were randomly assigned using a minimization algorithm to receive a formulation containing L-theanine plus lemon balm, valerian, and saffron extracts, or placebo, during 6 weeks. Objective sleep quality parameters were measured using an actigraphy device. We enrolled and randomised 64 individuals, 31 from the active group and 27 from the placebo group completed the 6 week follow-up. Mean sleep efficiency remained unmodified in the active group, and increased by 3% in the placebo group, the between-group difference in the change was not statistically significant (p = 0.49). Total sleep time also improved more with placebo (13.0 vs. 1.33 min, p = 0.66). Time wake after sleep onset (WASO) decreased more in the active group (4.6% vs. 2.4%), but the difference was not significant (p = 0.33). Mean PSQI decreased by 3.11 points (32.3%) in the active group, and by 3.86 points (39.5%) in the placebo group (p = 0.41). SF-36 increased more with placebo (+ 18.3 in active, + 32.1 in placebo, p = 0.68). Salivary cortisol remained unchanged in both groups. No serious adverse events were reported. Among adults with impaired sleep, a nutraceutical combination did not improve objective or subjective sleep parameters more than a placebo infusion.
在这项随机、安慰剂对照试验中,睡眠质量受损的成年人(匹兹堡睡眠质量指数≥5)使用最小化算法随机分配,接受含有茶氨酸加柠檬香脂、缬草根和藏红花提取物的配方或安慰剂治疗 6 周。使用活动记录仪测量客观睡眠质量参数。我们共招募并随机分配了 64 名个体,其中 31 名来自活性组,27 名来自安慰剂组完成了 6 周的随访。在活性组中,睡眠效率保持不变,而在安慰剂组中增加了 3%,组间变化差异无统计学意义(p=0.49)。总睡眠时间也随着安慰剂的使用而得到改善(13.0 分钟比 13.33 分钟,p=0.66)。在活性组中,醒来后入睡时间(WASO)减少更多(4.6%比 2.4%),但差异无统计学意义(p=0.33)。匹兹堡睡眠质量指数(PSQI)在活性组中下降了 3.11 分(32.3%),在安慰剂组中下降了 3.86 分(39.5%)(p=0.41)。SF-36 在安慰剂组中增加更多(活性组增加 18.3,安慰剂组增加 32.1,p=0.68)。两组唾液皮质醇均无变化。未报告严重不良事件。在睡眠质量受损的成年人中,与安慰剂输注相比,营养组合并未改善客观或主观睡眠参数。