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The effect of transcranial electrical stimulation on major depression.

Comparison of the effectiveness of different currents of one milliampere and two milliampere and sham (tDCS) on symptom severity, social cognition, working memory and risky decision-making in patients with major depressive disorder

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220421054607N2
Enrollment
60
Registered
2026-05-28
Start date
2025-06-22
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Major depressive disorder.

Interventions

Intervention group:Two intervention groups and a sham group: One intervention group will receive one milliampere stimulation and the other two milliampere stimulation in the F3 and F4 areas, two twent

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) to be 18 to 60 years of age, (2) to fail to at least one antidepressant medication, (3) not to be on current antidepressant medication or having stable treatment regime for at least 4 weeks before the experiment, (4) unipolar depression diagnosis according to Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5), criteria and confirmed by psychiatrists using the mini international Neuropsychiatric Interview (MINI), and (5) screened and qualified for brain stimulation interventions. Patients had to have a score of 17 points or more on the 17-item Hamilton Depression Rating Scale (HDRS; scores range from 0 to 52, with higher scores indicating more depression; a score of 24 or more indicates severe depression; minimal clinically significant difference, 3 points) as well as a low risk of suicide (evaluated with the use of the MINI). Other psychiatric or relevant neurological diseases and co-morbidities will be excluded.

Exclusion criteria

Exclusion criteria: Exclusion criteria: Having any other psychiatric disorders, including bipolar, psychotic, and obsessive-compulsive spectrum disordersHaving a chronic medical condition Having epilepsy and other neurological disorders Having a history of head traumaUse of drugs and alcohol Having metal implants in the head Receiving psychological treatments for at least one month prior to entering the study

Design outcomes

Primary

MeasureTime frame
Depression, transcranial electrical stimulation. Timepoint: Measurements of depression, working memory, social cognition, and risky decision-making before and after the intervention and three months after the intervention. Method of measurement: The Beck Depression Inventory (BDI-II) (for screening) and Hamilton (for measuring depression severity) are obtained, the Motor Orientation Test (MOT) is a training method designed to calm the client and introduce them to the computer and touch screen. It should always be administered at the beginning of the test session, the ERT for measuring social cognition, the CGT for risky decision-making, the SWM for working memory.

Secondary

MeasureTime frame
Depression severity score, social cognition score, working memory score, risky decision-making score. Timepoint: Before and after the intervention and three months after the intervention. Method of measurement: To measure social cognition ERT To measure working memory WMS To measure risky decision-making CGT.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParinaz Sadat Amiri Sararudi

Qazvin University of Medical Sciences

ami.parinaz399@gmail.com+98 24 3354 4000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026