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The effect of transcranial direct current stimulation on depression patients and the effect of resting state brain functional connectivity

The effect of transcranial direct current stimulation on depression patients and the effect of resting state brain functional connectivity

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088119
Enrollment
Unknown
Registered
2024-08-12
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

depressive disorder

Interventions

Depression group:Conventional drug therapy plus 2mA transcranial direct current stimulation for 30 minutes daily, for a duration of 4 weeks, 5 times per week, totaling 20 sessions.
Healthy control:Conventional medical treatment only.

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1.The patient meets the diagnostic criteria for depression according to the International Classification of Diseases (ICD-10); 2.The patient is experiencing the first episode of depression, or has not used antidepressants, mood stabilizers, or antipsychotic medications for the two weeks prior to treatment initiation; 3.The Hamilton Depression Rating Scale score is greater than 20; 4.The patient is aged between 13 and 35 years, with no gender restriction; 5.The patient is right-handed; 6.The patient has no history of substance abuse or alcohol dependence; 7.The patient's condition and vital signs are stable, with no other severe complications such as respiratory failure, heart failure, or pulmonary infection; 8.The patient has signed an informed consent form prior to undergoing transcranial direct current stimulation (tDCS) therapy and voluntarily participates in this study.

Exclusion criteria

Exclusion criteria: 1.Presence of suicidal ideation, diagnosis of bipolar affective disorder; 2.Comorbid with other psychiatric disorders, cranial trauma; 3.History of previous epileptic seizures or unexplained loss of consciousness; 4.Currently participating in other clinical trials; 5.Undergoing other non-invasive neurostimulation, magnetic stimulation, or similar neuromodulation therapies.

Design outcomes

Primary

MeasureTime frame
HAMD;

Secondary

MeasureTime frame
Near-infrared brain imaging examination;SDS;

Countries

China

Contacts

Public ContactYujun Li

Affiliated Hospital of North Sichuan Medical College

sammyleee@163.com+86 153 5127 5718

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026