Inclusion criteria: |
  1. Aged 18 to 65 years |
  2. Right-handed |
  3. Diagnosed with MDD based on DSM-5 criteria by at least one qualified psychiatrist |
  4. 24-item Hamilton Rating Scale for Depression (HAMD-24) score ≥ 17 |
  5. Completed ECT treatment |
  6. Capable of comprehending and completing the study assessments |
  7. Written informed consent provided by patients and/or their legal guardians |
Exclusion criteria: |
  1. Severe systemic illnesses (e.g., hepatic, renal, respiratory, cardiovascular, endocrine, hematological, oncological diseases) |
  2. Diagnosis of schizophrenia, bipolar disorder, dementia, substance dependence or abuse, or any primary psychotic disorder according to DSM-V criteria |
  3. Skin lesions or dermatological issues at electrode sites |
  4. Metal implants or electrically sensitive devices |
  5. Neurological conditions (e.g., stroke, seizure disorders) affecting cognition or treatment response |
  6. ECT within the past six months |
  7. Known hypersensitivity or contraindication to concurrent ECT medications |
  8. Pregnant or lactating |
  9. Receiving transcranial magnetic stimulation or other neuromodulation treatments |
  10. Participation in another concurrent clinical trial |