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Acupuncture Regulates Default Mode Network of Chronic Insomnia Disorder Patients : A fMRI Study

Acupuncture Regulates Emotion-cognitive Network of Chronic Insomnia Patients : A DTI-fMRI Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03386903
Enrollment
90
Registered
2017-12-29
Start date
2018-02-28
Completion date
2019-06-28
Last updated
2017-12-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Insomnia

Brief summary

The purpose of the study is to investigate the underlying central nervous mechanisms of acupuncture treatment in chronic insomnia patients, from observation changes of gray matter and functional connectivity in the default mode network and the salience network by functional magnetic resonance imaging, and combine with clinical efficacy assessment to analyze the association between the results of imaging and behavioristic.

Detailed description

Chronic insomnia which can cause daytime function impairments like abnormal emotion and hypomnesis is important risk factors for developing cardiovascular disease, neurological disorders or mental disorders. Acupuncture is a widely recognized therapy to treat chronic insomnia in clinical practice. Previous researches presented that sleep-wake dysfunction of patients with chronic insomnia have strong correlation with abnormal of the default mode network and salience network. The project present acupuncture may improve sleep quality by adjusting the abnormal default mode network and the salience network in patients with chronic insomnia. The investigators are assigned the ninety eligible participants in three groups: thirty chronic insomnia patients by true acupuncture treatment (Zhoushi coordinated points), thirty chronic insomnia patients by sham acupuncture stimulation (non-acupoint points) and thirty healthy subjects, Treatment will be given 3 times per week for 3 months. Additionally, two methods include functional magnetic resonance imaging (fMRI) and clinical scales evaluation as the outcome measures to evaluate the effectiveness and security of acupuncture. Outcomes will be evaluated at baseline and 3 month post-treatment. The aim of this project is to investigate effect of acupuncture treatment on gray matter and functional connectivity of the default network and the salience network in chronic insomnia patients, and to analyze the association between sleep quality, emotion, day function with imaging results. The central nervous mechanisms underlying acupuncture treatment are discussed by this finding which may provide scientific basis for acupuncture treatment in chronic insomnia.

Interventions

Patients receive true acupuncture treatment by Zhoushi coordinated points at the Bai-hui (DU20), Shen-ting (DU24), bilateral Ben-shen (BG13), Shen-men (HT7), San-yin-jiao (SP6) with Deqi sensation. The needles are retained for 20 minutes in every course, three times per week and last for 3 months.

DEVICESham acupuncture

Patients receive sham acupuncture stimulation by non-acupoint points (superficial insertion, 0.2 cun, No needle sensation (de qi) is elicited) at the bilateral mid-point between Shuaigu(GB8) and Touwei(ST8), Touwei(ST8) and Yangbai(GB14), front tibia, the junction of biceps and triceps.

Sponsors

Beijing Hospital of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Insomnia group: Patients must meet DSM V criteria for chronic insomnia. PSQI\>7 、ISI\>7、 SAS\<50、 SDS\<50. * control group: no self-reported sleep problems in the last 1 months. PSQI≤5 、SAS\<50、 SDS\<50,MMSE≥27. * 30-60 years old. * Male or female. * Dextromanuality. * Having given written informed consent to participate in the research project.

Exclusion criteria

* History of cardiovascular and respiratory diseases. * Other diagnoses of the nerve or mental disorders. * Other sleep disorders. * The long history of smoking, drinking and abusing drugs, or taking psychotropic drugs in last month, and treatment in other clinical trials at the same time. * The body carrying pacemakers, defibrillators, implantable vascular clamp, implantable electric or magnetic device, mechanical heart valve, artificial cochlear, el., fMRI taboo and the claustrophobic. * MRI scans have been used to identify patients with a definite organic lesion or severe head anatomical asymmetry * Pregnancy, lactation and peri menopausal women. * An allergy history of syncope, alcohol, and metal needle. * The body Mass Index\>32 or \<19.8.

Design outcomes

Primary

MeasureTime frameDescription
Sleep quality obtained by questionnaire:Pittsburgh Sleep Quality Indexbaseline,12 weeksChange in Pittsburgh sleep quality index scores at the baseline and the end of 12 weeks stimulation with acupuncture.Minimum Score = 0 (good sleep); Maximum Score = 30 (disrupted sleep)

Secondary

MeasureTime frameDescription
Total sleep time obtained by questionnaire:Pittsburgh Sleep Quality Indexbaseline,12 weeks
Sleep efficiency obtained by questionnaire:Pittsburgh Sleep Quality Indexbaseline,12 weeks
Sleep latency obtained by questionnaire:Pittsburgh Sleep Quality Indexbaseline,12 weeks
Wake after sleep onset obtained by questionnaire:Pittsburgh Sleep Quality Indexbaseline,12 weeks
Sleep problem obtained by questionnaire:Insomnia Severity Indexbaseline,12 weeks
Brain gray matterbaseline,12 weeksThe changes of gray matter volume in default network before and after treatment
Emotional state of depression obtained by questionnaire:Self-Rating Depression Scalebaseline,12 weeks
Daytime function obtained by questionnaire:Epworth Sleepiness Scorebaseline,12 weeks
Daytime function obtained by questionnaire:Flinders Fatigue Scalebaseline,12 weeks
resting-state functional magnetic resonance imagingbaseline,12 weeksResting state intrinsic connectivity within the default network by MRI
Emotional state of anxiety obtained by questionnaire:Self-Rating Anxiety Scalebaseline,12 weeks

Countries

China

Contacts

Primary ContactLiu c zhi, M.D
lcz623780@126.com010-52176043
Backup Contactzhou ping, Postgraduate Student
hzyyzp@126.com13261306969

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026