Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Shanghai Mental Health Center, Shanghai Jiaotong University of Medicine, Shanghai, China.
BMJ Open. 2019 Apr 20;9(4):e021484. doi: 10.1136/bmjopen-2018-021484.
Sleep disorders including insomnia occur frequently in depressive patients. Acupuncture is a widely recognised therapy to treat depression and sleep disorders in clinical practice. This multicentre randomised controlled trial (RCT) is aimed to investigate the efficacy and safety of electroacupuncture (EA) in the treatment of depression patients with insomnia.
We describe a protocol for a multicentre RCT. A total of 270 eligible patients in three different healthcare centres in Shanghai will be randomly assigned to one of these three groups: treatment group (EA + standard care), control A group (sham electroacupuncture + standard care) and control B group (standard care). Treatment will be given three times per week for 8 consecutive weeks. The primary outcome is the Pittsburgh Sleep Quality Index. The secondary outcomes are sleep parameters recorded in the actigraphy, Hamilton Rating Scale for Depression score and Self-rating Anxiety Scale score. Daily dose of patients' antidepressant and sedative-hypnotic medication will be recorded in the dairy. All adverse effects will be assessed by the Treatment Emergent Symptom Scale. Outcomes will be evaluated at baseline, 4 weeks post-treatment and 8 weeks post-treatment, as well as at 1-month, 3-month and 6-month follow-up.
The trial has been approved by the Ethics Committee of Shanghai Municipal Hospital of Traditional Chinese Medicine (2017SHL-KY-04). Written informed consent will be obtained from all participants. The results of this study will be published in peer-reviewed journals or presented at academic conferences.
NCT03122080; Pre-results.
睡眠障碍包括失眠在抑郁患者中很常见。针灸是一种广泛认可的治疗方法,可在临床实践中治疗抑郁症和睡眠障碍。本多中心随机对照试验(RCT)旨在研究电针对失眠抑郁症患者的疗效和安全性。
我们描述了一项多中心 RCT 的方案。共有来自上海三个不同医疗机构的 270 名符合条件的患者将被随机分为三组:治疗组(电针+标准治疗)、对照组 A 组(假电针+标准治疗)和对照组 B 组(标准治疗)。治疗将每周进行三次,连续 8 周。主要结局是匹兹堡睡眠质量指数。次要结局是活动记录仪记录的睡眠参数、汉密尔顿抑郁量表评分和自评焦虑量表评分。患者抗抑郁药和镇静催眠药的每日剂量将在日记中记录。所有不良反应将通过治疗突发症状量表进行评估。结果将在基线、治疗后 4 周和治疗后 8 周以及治疗后 1 个月、3 个月和 6 个月进行评估。
该试验已获得上海市中医医院伦理委员会的批准(2017SHL-KY-04)。将从所有参与者处获得书面知情同意。本研究的结果将发表在同行评议的期刊上或在学术会议上展示。
NCT03122080;预结果。