College of Pharmacy, University of Minnesota, Minneapolis, MN, USA.
Explore (NY). 2011 Mar-Apr;7(2):76-87. doi: 10.1016/j.explore.2010.12.003.
The aim of this study was to investigate the potential of mindfulness-based stress reduction (MBSR) as a treatment for chronic primary insomnia.
A randomized controlled trial was conducted.
The study was conducted at a university health center.
Thirty adults with primary chronic insomnia based on criteria of the Diagnostic and Statistical Manual of Mental Disorders, Text Revision, 4th Edition were randomized 2:1 to MBSR or pharmacotherapy (PCT).
Mindfulness-based stress reduction, a program of mindfulness meditation training consisting of eight weekly 2.5 hour classes and a daylong retreat, was provided, with ongoing home meditation practice expectations during three-month follow-up; PCT, consisting of three milligrams of eszopiclone (LUNESTA) nightly for eight weeks, followed by three months of use as needed. A 10-minute sleep hygiene presentation was included in both interventions.
The Insomnia Severity Index (ISI), Pittsburgh Sleep Quality Index (PSQI), sleep diaries, and wrist actigraphy were collected pretreatment, posttreatment (eight weeks), and at five months (self-reports only).
Between baseline and eight weeks, sleep onset latency (SOL) measured by actigraphy decreased 8.9 minutes in the MBSR arm (P < .05). Large, significant improvements were found on the ISI, PSQI, and diary-measured total sleep time, SOL, and sleep efficiency (P < .01, all) from baseline to five-month follow-up in the MBSR arm. Changes of comparable magnitude were found in the PCT arm. Twenty-seven of 30 patients completed their assigned treatment. This study provides initial evidence for the efficacy of MBSR as a viable treatment for chronic insomnia as measured by sleep diary, actigraphy, well-validated sleep scales, and measures of remission and clinical recovery.
本研究旨在探讨正念减压(MBSR)作为慢性原发性失眠治疗方法的潜力。
采用随机对照试验。
该研究在一所大学健康中心进行。
30 名符合《精神障碍诊断与统计手册》第 4 版修订本(DSM-IV-TR)原发性慢性失眠标准的成年人被随机分为 MBSR 组或药物治疗(PCT)组,比例为 2:1。
提供正念减压治疗,这是一个正念冥想训练计划,包括每周 2.5 小时的 8 次课程和 1 天的静修,在三个月的随访期间要求进行家庭冥想练习;PCT 包括每晚 3 毫克的eszopiclone(LUNESTA),持续 8 周,然后按需使用三个月。两种干预措施都包括 10 分钟的睡眠卫生讲座。
采用失眠严重程度指数(ISI)、匹兹堡睡眠质量指数(PSQI)、睡眠日记和腕部活动记录仪在治疗前、治疗后(8 周)和 5 个月(仅自我报告)收集。
与基线相比,MBSR 组的活动记录仪测量的入睡潜伏期(SOL)在 8 周内减少了 8.9 分钟(P<0.05)。在 MBSR 组中,从基线到 5 个月的随访,ISI、PSQI 和日记测量的总睡眠时间、SOL 和睡眠效率均有显著改善(P<0.01,均)。PCT 组也发现了类似幅度的变化。30 名患者中有 27 名完成了他们的分配治疗。本研究初步证明了 MBSR 作为一种可行的慢性失眠治疗方法的疗效,通过睡眠日记、活动记录仪、经过充分验证的睡眠量表以及缓解和临床康复的衡量标准进行评估。