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A Study on Cognitive Enhancement via Temporal Interference Non-Invasive Deep Brain Stimulation in Schizophrenia Patients.

A Study on Cognitive Enhancement via Temporal Interference Non-Invasive Deep Brain Stimulation in Schizophrenia Patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123630
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-04-28
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Schizophrenia

Interventions

Sponsors

The Sixth Hospital of Changchun
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for schizophrenia as defined by the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5); 2. Individuals aged 18–45 years, with no sex restriction; 3. Educational level of junior high school or above; 4.Right-handed,with the ability to comprehend the questionnaires and verbal instructions involved in the study, and willing to participate in the study. 5.PANSS negative subscore >=20; 6.With adequate auditory and visual acuity to complete the required assessments.

Exclusion criteria

Exclusion criteria: 1.Diagnosis of any DSM-5 Axis I disorder other than schizophrenia; 2.Severe psychotic symptoms that preclude the patient from completing the required assessments; 3. Presence of suicidal ideation or high suicide risk; 4.Current severe physical illness or central nervous system disorder, or substance abuse; 5. Pregnancy, planned pregnancy in the near future, or breastfeeding; 6.The subject needs to be withdrawn due to health risks; 7.The subject voluntarily requests to withdraw from the study; 8.During the intervention, it becomes necessary to adjust psychiatric medication, or to administer physical therapy or psychological therapy.

Design outcomes

Primary

MeasureTime frame
Positive and negative symptoms;

Secondary

MeasureTime frame
Cognitive function;

Countries

China

Contacts

Public ContactMin Wang

The Sixth Hospital of Changchun

13894888485@163.com+86 431 81968536

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026