Jiao Yue, Guo Xiao, Luo Man, Li Suxia, Liu Aihua, Zhao Yufeng, Zhao Bin, Wang Dequan, Li Zaifang, Zheng Xiaojiao, Wu Mozheng, Rong Peijing
Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing 100700, China.
National Institute on Drug Dependence, Peking University, Beijing 100191, China.
Evid Based Complement Alternat Med. 2020 Aug 6;2020:6049891. doi: 10.1155/2020/6049891. eCollection 2020.
Insomnia inflicts mental burden and decreases physical productivity and affects life quality. Transcutaneous vagus nerve stimulation (ta-VNS) may be an effective treatment option for insomnia. This study aims to evaluate the effect and safety of ta-VNS and compare it with transcutaneous nonvagus nerve stimulation (tn-VNS). A multicenter, randomized, clinical trial was conducted at 3 hospitals in China enrolling 72 insomnia participants from May 2016 to June 2017. Participants were randomly assigned (1 : 1) to receive 40 sessions of ta-VNS or tn-VNS treatment. 63 participants completed the trial. ta-VNS treatment significantly decreased the Pittsburgh Sleep Quality Index score, Epworth Sleepiness Scale score, Flinders Fatigue Scale score, Hamilton Depression Scale score, and Hamilton Anxiety Scale score over 4 weeks compared with those of the baseline. Moreover, it also significantly increased the 36-item Short-Form Health Survey Questionnaire scores compared with that of the baseline. However, it did not show significant differences compared with tn-VNS in changes of primary and secondary outcomes. The incidence of adverse events was low. ta-VNS significantly relieved insomnia over 4 weeks. Moreover, it also alleviated fatigue and improved participants' quality of life as well as other concomitant symptoms such as depression and anxiety. This trial is registered at Chinese Clinical Trial Registry (http://www.chictr.org.cn) with the registration number: ChiCTR-TRC-13003519.
失眠会造成精神负担,降低身体机能,并影响生活质量。经皮迷走神经刺激(ta-VNS)可能是治疗失眠的一种有效方法。本研究旨在评估ta-VNS的疗效和安全性,并将其与经皮非迷走神经刺激(tn-VNS)进行比较。2016年5月至2017年6月,在中国的3家医院进行了一项多中心、随机临床试验,招募了72名失眠患者。参与者被随机分配(1∶1)接受40次ta-VNS或tn-VNS治疗。63名参与者完成了试验。与基线相比,ta-VNS治疗在4周内显著降低了匹兹堡睡眠质量指数评分、爱泼华嗜睡量表评分、弗林德斯疲劳量表评分、汉密尔顿抑郁量表评分和汉密尔顿焦虑量表评分。此外,与基线相比,它还显著提高了36项简明健康调查问卷评分。然而,在主要和次要结局的变化方面,与tn-VNS相比,它没有显示出显著差异。不良事件的发生率较低。ta-VNS在4周内显著缓解了失眠。此外,它还减轻了疲劳,改善了参与者的生活质量以及其他伴随症状,如抑郁和焦虑。本试验已在中国临床试验注册中心(http://www.chictr.org.cn)注册,注册号为:ChiCTR-TRC-13003519。