Insomnia disorder
Conditions
Interventions
Experimental group:Transcranial time interference electrical stimulation
Control group:Simulate true excitement
Sponsors
Affiliated Kangning Hospital of Ningbo University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1.It meets the diagnostic criteria for non-organic insomnia in the International Classification of Diseases, Tenth Revision, 10th (ICD-10). 2.Conform to the diagnostic criteria for insomnia in the International Classification of Sleep Disorders, 3rd edition (ICSD-3); 3.The Pittsburgh sleep quality index (PSQI) score was greater than 5 points before treatment; 4.No concurrent mental disorders such as depression and anxiety, nor neurological diseases such as stroke, dementia, Parkinson's disease, and chronic pain; 5.Age range of 18 to 60 years old, gender not limited; 6.Primary school education or above; 7.Patients voluntarily participated in this study and signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Physical illness, organic brain disease and history of substance abuse; 2.Individuals with a history of epileptic seizures; 3.People with metal objects such as pacemakers, stents, and inner ear hearing AIDS in their bodies; 4.Combined with other mental disorders; 5.Pregnant or lactating women; 6..Check for those who are uncooperative or unable to complete the experiment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in Pittsburgh Sleep Quality Index (PSQI) before and after intervention and during follow-up; | — |
Secondary
| Measure | Time frame |
|---|---|
| Remission rate and response rate on the Hamilton Depression Rating Scale (HAMD-17) before and after intervention follow-up;Remission rate and response rate of the Hamilton Anxiety Scale (HAMA) before and after intervention; | — |
Countries
China
Contacts
Public ContactQi Zhou
Affiliated Kangning Hospital of Ningbo University
Outcome results
None listed