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Efficacy and Safety of transcranial alternating current stimulation for Depression: a Multicenter RCT Study

A study of the efficacy of transcranial alternating current stimulation for patients with depression

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103570
Enrollment
Unknown
Registered
2025-05-30
Start date
2024-11-16
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Depressive Disorder

Interventions

active tACS:The active tACS protocol lasted for 40 min of continuous sine-wave stimulation with the frequency of 10Hz and an amplitude ranging from 1.5mA to 2.0mA, adjusted according to the tolerabili
sham tACS:we use fade-in, short-stimulation, fade-out (FSF) stimulation pattern, with 30s-long fade-in/out periods. The same parameters as in the active group are used at the beginning and the end of

Sponsors

Ruijin Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: a. Clinical diagnosis of depressive disorder according to criteria of ICD-10; b. Age ranges between 18 and 65 years; c. HDRS-17 score equals to or above 8; d. No medical history/Under stable antidepressant treatment in one month; e. Ability and willingness to provide written informed consent; f. Good compliance, able to cooperate with follow-up visits.

Exclusion criteria

Exclusion criteria: a. Combination of other psychotic disorders and neurological diseases; b. Severe personality disorders; c. History of organic brain disease or previous seizures; d. History of invasive brain surgeries, including deep brain stimulation and non-invasive neurostimulation treatments, including electroconvulsive therapy (ECT), transcranial magnetic stimulation (TMS), transcranial direct current stimulation (tDCS), and transcranial alternating current stimulation (tACS), etc. e. Any circumstances (family support, medical, psychological, social or geographical factors) that may endanger the patient's safety or prevent the patient from successfully participating in the study at present or in the future;

Design outcomes

Primary

MeasureTime frame
Differences of Hamilton Depression Scale score reduction rates in two groups;

Secondary

MeasureTime frame
Differences of treatment efficacy rates in two group ;

Countries

China

Contacts

Public ContactBomin Sun

Ruijin Hospital, Shanghai JiaoTong University School of Medicine

bomin_sun@163.com+86 138 1777 7401

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 30, 2026