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The Effect of the High-definition Transcranial Direct Current Stimulation (HD-tDCS) on Treatment-Resistant Schizophrenia

The Effect of the High-definition Transcranial Direct Current Stimulation (HD-tDCS) on Treatment-Resistant Schizophrenia: a Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062702
Enrollment
Unknown
Registered
2022-08-16
Start date
2022-08-17
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

Schizophrenia

Interventions

High-definition Transcranial Direct Current Stimulation (FZ positive):High-definition Transcranial Direct Current Stimulation (FZ positive)
High-definition Transcranial Direct Current Stimulation(FZ negative):High-definition Transcranial Direct Current Stimulation(FZ negative)

Sponsors

Beijing Huilongguan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. A diagnosis of schizophrenia based on the Diagnostic and Statistical Manual of Mental Disorders,5th Edition (DSM-5) 2. >= 2 past adequate treatment episodes with different antipsychotics and poor response; 3. Equivalent to >= 600 mg of chlorpromazine per day and >= 6 weeks at a therapeutic dosage; 4. PANSS >=70 and CGI-SI >=4; 5. 18–60 years of age; 6. Education years >= 6 years; 7. Right handedness; 8. Voluntarily participate and sign the informed consent (participants and/or legal guardian).

Exclusion criteria

Exclusion criteria: 1. The patient is participating in another interventional study or the patient has participated in another interventional study within the past three months; 2. Contraindications of using HD-tDCS (e.g.: intracranial metal foreign body, cochlear implant, intracranial hypertension); 3. With mental retardation or organic brain disease; 4. Severe weakness, impulsivity, excitement, and uncooperative; 5. Combination of severe depression, anxiety, or substance dependence (excluding nicotine); 6. Organic disabilities in hearing or/visual perception impairment; 7. Unstable or serious physical illness or severe side effect (e.g.: Drug-induced extrapyramidal syndrome, tardive dyskinesia); 8. Pregnancy or breastfeeding; 9. Immunomodulators, neurotropic, and antioxidants use within eight weeks; 10. Infections within two weeks.

Design outcomes

Primary

MeasureTime frame
Severity of Clinical symptoms;

Secondary

MeasureTime frame
Cognition;Personal and Social performance;Clinical Global Impression;Metabolites of the tryptophan pathway;imaging data;

Countries

China

Contacts

Public ContactYunlong Tan

Beijing Huilongguan Hospital

yltan21@126.com+86 10 83024523

Outcome results

None listed

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