Randomized controlled trial for electroacupuncture for depression and its related metabolomics research
- Conditions
- depression
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- Not specified
1. Male or female participants aged 18-70 years;
2. Participants who meet the diagnostic criteria of depression according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV);
3. Participants whose HAMD score 20-35;
4. Participants who have complaint about insomnia at the first visit to the doctor;
5. Participants who voluntarily agree with the investigation and sign a written informed consent form for the clinical trial.
1. Participants with secondary depressive disorders caused by organic diseases, medicine, or psychotic disorders including schizophrenia, etc;
2. Participants who are in the depressive episode of bipolar disorder, or suffering from dysthymia, reactive depression and depressive syndrome caused by other diseases;
3. Participants with alcohol abuse or drug dependence;
4. Participants who refuse to wear the Actigraphy during the trial;
5. Pregnant or breast-feeding women.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method HAMD;
- Secondary Outcome Measures
Name Time Method TESS;SDS;