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Accelerating theta bursts to improve the efficacy and neuromechanism of prospective memory in schizophrenia

Accelerating theta bursts to improve the efficacy and neuromechanism of prospective memory in schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111615
Enrollment
Unknown
Registered
2025-11-03
Start date
2025-11-09
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Schizophrenia

Interventions

Real stimulus:a-iTBS real intervention
pseudo-stimulation:Sham a-iTBS intervention

Sponsors

Affiliated Kangning Hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Meet the diagnostic criteria for schizophrenia in the Diagnostic and Statistical Manual of Mental Disorders (Fifth Edition, DSM-5); 2) Age between 18 and 60 years; 3) Patients have received current medication treatment for at least 4 weeks with stable psychiatric symptoms, and are currently able to cooperate with iTBS therapy; 4) Positive and negative symptom scales scores should not exceed 5 points for: P1 Delusions, P3 Hallucinatory Behaviors, P5 Grandiosity, P6 Suspicion/Paranoia, G9 Abnormal Thought Content; 1.and should not exceed 4 points for: P2 Disorganized Thinking; 5) Obtain written informed consent from patients and their families.

Exclusion criteria

Exclusion criteria: 1) Patients with severe physical or neurological disorders, or those exhibiting significant abnormalities in biochemical indicators, electroencephalogram (EEG), or electrocardiogram (ECG); 2) Individuals displaying demonstrable negative, impulsive, or disruptive behaviors that impair examination compliance; 3) Subjects deemed by investigators to pose high suicide or violent risks; 4) Participants who received electroconvulsive therapy or magnetic stimulation within three months prior to enrollment; 5) Those with claustrophobia making MRI scanning inadvisable; 6) Patients with implanted metallic or electronic devices such as intracranial metal objects, cochlear implants, cardiac pacemakers, or stents; 7) Individuals at risk of epileptic seizures, including history of cranial trauma, alcohol abuse, abnormal EEG patterns, MRI evidence of brain structural abnormalities, or family epilepsy history; 8) Pregnant women, those planning pregnancy, or those with unanticipated pregnancy risks.

Design outcomes

Primary

MeasureTime frame
Electrophysiological indicators;

Secondary

MeasureTime frame
PANSS;Neuropsychological measurements related to cognitive behavior;

Countries

China

Contacts

Public ContactRong Wang

Affiliated Kangning Hospital of Ningbo University

525250613@qq.com+86 574 2630 2572

Outcome results

None listed

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