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Clinical Trials/ITMCTR2100005324
ITMCTR2100005324
Not yet recruiting
未知

Investigate the clinical efficacy and central brain mechanisms of transcutaneous auricular acupoint vagus nerve stimulation in the treatment of patients with insomnia disorder based on multimodal MRI

Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences0 sitesTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Insomnia Disorder
Sponsor
Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • 1\) Conformity to the diagnostic standards of the American Diagnostic and Statistical Manual of Mental Disorders (5th edition) for PI. 2\) Insomnia symptoms lasting for \> 3 months, \=3 times per week. 3\) 18 to 70 years old, right\-handed. 4\) Pittsburgh sleep quality index (PSQI) score\=8,17 items of the Hamilton Depression Scale \=17 and 14 items of the Hamilton Anxiety Scale \=14\. 5\) Not taking any neuropsychiatric medications or substances and not receiving acupuncture treatment in the past month. 6\) Cooperate to accept the treatment of auricular electrical stimulation and complete the acquisition of magnetic resonance data. 7\) Signed the informed consent form..

Exclusion Criteria

  • 1\) Patients with severe physical diseases, such as coronary heart disease, malignant tumor and renal failure. 2\) Patients with brain organic diseases. 3\) Combined with any other mental disorder, personality disorder or psychoactive substance abuse or dependence. 4\) Patients who cannot elute from medicine or acupuncture treatment. 5\) Pregnant and lactating women. 6\) Patients with contraindications of magnetic resonance imaging (MRI). 7\)Patients with damaged ear skin. 8\)Patients who were unwilling to sign inform consent.

Outcomes

Primary Outcomes

Not specified

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