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Search / Trial NCT07074704

tACS to Improve Negative Symptoms & Cognition in Long-term Hospitalized Schizophrenia Patients.

Launched by TONGJI UNIVERSITY · Jul 10, 2025

Trial Information

Current as of September 04, 2025

Enrolling by invitation

Keywords

ClinConnect Summary

1. Research purpose (1) This study aims to explore the synergistic therapeutic effect of tACS on negative symptoms and cognitive function in long-term hospitalized schizophrenia patients; (2) Using emotion-induced EEG activity in a virtual reality context as a biomarker, analyze its correlation with the clinical efficacy of tACS.
2. Expected results (1) It is confirmed that tACS can improve negative symptoms and cognitive function in long-term hospitalized schizophrenia patients; (2) Biomarkers can be used to predict the efficacy of tACS in improving negative symptoms and cognitive function...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • * Inclusion criteria for long-term hospitalized schizophrenia patients:
  • 1. Diagnosed with DSM-5 schizophrenia and hospitalized for more than half a year
  • 2. Aged between 18 and 65 years old
  • 3. Willing to participate in the study and sign the informed consent
  • 4. Stable condition, PANSS total score changed less than 15% at least 2 months before the study.
  • 5. Education level above primary school
  • 6. Normal vision or normal after correction
  • Inclusion criteria for normal control group:
  • 1. No diagnosed mental illness
  • 2. Aged between 18 and 65 years old
  • 3. Willing to participate in the study and sign the informed consent
  • 4. Education level above primary school
  • 5. Normal vision or normal after correction
  • 6. Residents living in Pudong community
  • Exclusion Criteria:
  • Exclusion criteria for long-term hospitalization of schizophrenia patients:
  • 1. Combined diagnosis of other mental illnesses in DSM-5
  • 2. History of severe neurological diseases, epilepsy, craniocerebral trauma, etc.
  • 3. Severe organic diseases of the heart, liver, kidney and other organs that are unstable
  • 4. Infectious skin diseases
  • 5. Use of other drugs that affect the results during the study, such as benzodiazepines, non-benzodiazepine sedatives, and psychostimulants
  • 6. Pregnant or lactating women
  • 7. Patients with claustrophobia
  • 8. Patients with alcohol, drugs Abuse history
  • 9. Patients who have received TACS treatment in the past and have no effect or intolerance
  • Exclusion criteria for normal control group:
  • 1. Patients with a history of severe neurological diseases, epilepsy, craniocerebral trauma, etc.
  • 2. Patients with severe organic diseases that cause instability of organs such as heart, liver, and kidney
  • 3. Patients with infectious skin diseases
  • 4. During the study, drugs that affect the results were used in combination, such as benzodiazepines, non-benzodiazepine sedatives, and psychostimulants
  • 5. Pregnant or lactating women
  • 6. Patients with claustrophobia
  • 7. Patients with a history of alcohol and drug abuse -

About Tongji University

Tongji University, a prestigious institution located in Shanghai, China, is renowned for its commitment to advancing medical research and education. As a clinical trial sponsor, Tongji University leverages its extensive resources and expertise in various fields of healthcare to facilitate innovative clinical studies aimed at improving patient outcomes. The university collaborates with leading researchers and healthcare professionals to conduct rigorous trials that adhere to international standards of scientific integrity and ethical practice. Through its dedication to translational medicine and interdisciplinary collaboration, Tongji University plays a pivotal role in fostering advancements in medical science and addressing pressing health challenges.

Locations

Shanghai, Shanghai, China

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported