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临床试验/NCT03447587
NCT03447587已完成不适用

Determining the Role of Acupuncture in the Modulation of Peripheral Oxidative Stress in Patients With Insomnia: A Randomized Placebo-Controlled Trial

The Hong Kong Polytechnic University1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2018年3月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
140
试验地点
1
主要终点
Sleep efficiency (SE)

研究概览

简要总结

A randomized controlled trial involving 140 subjects with (Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition) DSM-5 insomnia disorder after excluding those with other medical conditions, psychiatric disorders, and sleep disorders that may cause insomnia. The subjects will be randomly assigned to either acupuncture treatment or sham acupuncture (control group) in a 1:1 ratio. The acupuncture treatment group will receive acupuncture treatments using a semi-standardized protocol. In a similar way, the sham acupuncture control group will receive acupuncture using validated non-invasive sham acupuncture needles. Both subjective (the sleep questionnaire and sleep diary) and objective (actigraphy) outcome measures will be recorded at baseline and at 1- and 5-week post-treatment. Fasting blood samples will be taken on the morning of the assessments at these time points to measure the oxidative stress parameters, including the malondialdehyde (MDA) level, and the glutathione peroxidase (GPx), paraoxonase (PON), and arylesterase (ARE) activities. The primary outcome is sleep efficiency, measured using a 7-day sleep diary and the oxidative stress parameters at 1-week post-treatment.

详细描述

Background: Insomnia is a very common complaint worldwide. Acupuncture is an alternative treatment for improving sleep quality. However, its efficacy and mechanism of action as a treatment for insomnia requires further investigation. Acupuncture may attenuate oxidative stress which is thought to be an important pathophysiological factor in insomnia.

Aims: To evaluate the safety and efficacy of a semi-individualized acupuncture treatment in improving sleep, and to examine its effects on oxidative stress parameters in subjects with primary insomnia disorder.

Methods: This will be a randomized controlled trial involving 140 subjects with DSM-5 insomnia disorder after excluding those with other medical conditions, psychiatric disorders, and sleep disorders that may cause insomnia. The subjects will be randomly assigned to either acupuncture treatment or sham acupuncture (control group) in a 1:1 ratio. The acupuncture treatment group will receive acupuncture treatments using a semi-standardized protocol. In a similar way, the sham acupuncture control group will receive acupuncture using validated non-invasive sham acupuncture needles. Both subjective (the sleep questionnaire and sleep diary) and objective (actigraphy) outcome measures will be recorded at baseline and at 1- and 5-week post-treatment. Fasting blood samples will be taken on the morning of the assessments at these time points to measure the oxidative stress parameters, including the malondialdehyde (MDA) level, and the glutathione peroxidase (GPx), paraoxonase (PON), and arylesterase (ARE) activities. The primary outcome is sleep efficiency, measured using a 7-day sleep diary and the oxidative stress parameters at 1-week post-treatment.

Data analysis: Changes in the sleep and oxidative stress outcome measures will be compared between groups by using a mixed-effects model at each time point. Correlations between sleep parameters and oxidative stress parameters will be examined using a Pearson correlation. Mediation analysis will be performed to explore the possible mediating effect of oxidative stress factors on sleep.

Significance: The relationship between oxidative stress and insomnia severity has been under-researched. To the best of our knowledge, there has thus far been no study on the effect of acupuncture on oxidative stress in subjects with insomnia disorder. The present study will not only provide high-quality evidence of the efficacy of acupuncture as a treatment for insomnia, but also of the associated changes in oxidative stress parameters. It will guide future studies on the treatment mechanism and pathophysiology of insomnia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hong Kong resident,
  • ethnic Hong Kong Chinese aged 18-65,
  • fulfilling diagnostic criteria of insomnia disorder using DSM-5 diagnostic criteria for Insomnia Disorder by Brief Insomnia Questionnaire,
  • Insomnia Severity Index total score ≥11 at screening and baseline visits,
  • willing to give informed consent and comply with the trial pr1otocol.

排除标准

  • any current or past major depressive disorder, generalized anxiety disorders or panic disorder, manic or hypomanic episode, substance use disorders, organic mental disorder, schizophrenia or any other psychotic disorder as defined by DSM-IV criteria using the Structured Clinical Interview for DSM-IV (SCID);
  • any current physical illnesses that contributes significantly to the subject's insomnia;
  • pregnancy;
  • a previous diagnosis of sleep apnea or periodic limb movement disorder (if subjects with symptoms suggestive of other sleep disorders, they will be referred to our psychiatrists for further assessment;
  • a Home Single-Channel Nasal Pressure (HNP) screening with apnea-hypopnea index (AHI) >5;
  • at significant risk of suicide according to SCID;
  • infection or abscess close to the site of the selected acupoints;
  • valvular heart defects, bleeding disorders or taking anticoagulant drugs, use of any implanted electrical device such as pacemaker, defibrillator, brain and nerve stimulators, etc.;
  • receiving acupuncture treatment in the past 6 months;
  • taking herbal remedies, over-the-counter medication or psychotropic drugs that target insomnia within the two weeks prior to baseline

结局指标

主要结局

Sleep efficiency (SE)

时间窗: Week 5

the sleep efficiency derived from 7 days sleep diary

次要结局

  • Sleep efficiency (SE)(Baseline, week 9)
  • Insomnia Severity Index (ISI)(Baseline, week 5, week 9)
  • Sleep onset latency (SOL)(Baseline, week 5, week 9)
  • Short Form Six Dimension (SF6D)(Baseline, week 5, week 9)
  • The activity of PON(Baseline, week 5)
  • Actigraphy: Sleep onset latency (SOL)(Baseline, week 5, week 9)
  • The level of MDA(Baseline, week 5)
  • The activity of GPx(Baseline, week 5)
  • The activity of ARE(Baseline, week 5)
  • Wake after sleep onset (WASO)(Baseline, week 5, week 9)
  • Total sleep time (TST)(Baseline, week 5, week 9)
  • Actigraphy: Total sleep time (TST)(Baseline, week 5, week 9)
  • Hospital Anxiety and Depression (HADS)(Baseline, week 5, week 9)
  • Actigraphy: Wake after sleep onset (WASO)(Baseline, week 5, week 9)
  • Actigraphy: Sleep efficiency (SE)(Baseline, week 5, week 9)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

YEUNG Wing Fai

Assistant professor

The Hong Kong Polytechnic University

研究点 (1)

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