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NCT07446478Completed

TIS for Improving Cognitive Impairment Associated With Schizophrenia

Efficacy and Safety of Time Interference Stimulation on Cognitive Impairment Associated With Schizophrenia

Source: ClinicalTrials.gov · Last updated 23 Sept 2026

Brief summary (registry, in English)

This study aims to evaluate the efficacy and safety of TIS targeting the hippocampus in ameliorating cognitive impairment associated with schizophrenia (CIAS). Participants will receive TIS twice a day for 2 weeks. Their clinical data, including the baseline clinical symptom scale score, cognitive function, and MRI data, will be collected at baseline and at the end of the 2-week intervention.

Status (registry)
Completed
Study type
Interventional
Enrollment
10 (actual)
First submitted
26 Feb 2026
Start date
24 Jun 2026
Primary completion date
16 Sept 2026
Lead sponsor
Central South University
NCT number
NCT07446478

What you commit to

  • Study type: Interventional
  • Participants enrolled: 10
  • From 24 Jun 2026 to the primary completion date, 16 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • with clear drug-induced extrapyramidal reaction;
  • have received other regimens of electrical or magnetic therapy in 1 month before enrollment.

Other illness

  • Presence of other psychiatric comorbidities, intellectual disability, obvious mood symptoms, or substance use disorders (other than caffeine and/or tobacco);
  • A history of seizures, meningitis, or encephalitis;
  • History of intracranial tumors or surgery;
  • history of severe head trauma;

Other

  • with contraindications to transcranial electrical stimulation;

Who the study is looking for

  • Age 18-50 years old;
  • meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth edition (DSM-5) diagnostic criteria;
  • the diagnosis of schizophrenia is confirmed by the Structured Clinical Interview for DSM-5 (SCID-5);
  • the disease duration does not exceed 8 years;
  • 1-2 antipsychotic drugs are taken, and the treatment dose of antipsychotic drugs was stable for at least 1 week before enrollment. Mood stabilizers, antidepressants, and excessive benzodiazepines (lorazepam when 2 doses exceeded 2 mg/d) are not allowed;
  • The type of antipsychotic drugs remains unchanged during treatment, and the dose is adjusted by no more than 25%;
  • Impaired functioning in daily activities;
  • The Global Deficit Score (GDS) for the MATRICS Consensus Cognitive Battery (MCCB) reaches 0.5 or above;
  • Agree to participate in this study and provide written informed consent

Age in the registry: 18 years to 50 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Second Xiangya Hospital, Central South University
Coordinator of this site? Confirm its status
ChangshaChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.