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Testing Brain Stimulation to Help Working Memory in Schizophrenia

Tests brain stimulation with a device against sham stimulation in adults with schizophrenia.

Plain-language title generated from the registry record
Registry title: tACS for Working Memory in Schizophrenia

Key facts

Where
Changsha, ChinaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18-50 with schizophrenia and weak working memory. They take 1-2 antipsychotic medicines at a stable dose.

Age
18-50 years
Sex
All sexes
Disease stage
Schizophrenia confirmed by DSM-5 criteria and an interview (SCID-5). Spatial span T-score below 40 on the MCCB. Daily activities are impaired.
Earlier treatment
Taking 1-2 antipsychotic medicines, with the dose stable for at least 1 week before joining. No mood stabilizers, antidepressants, or more than 2 mg/day lorazepam equivalent. No other electrical or magnetic stimulation in the last month.

Main reasons for not taking part

  • Any other mental disorder besides schizophrenia
  • Significant mood symptoms or substance use disorder (other than caffeine or tobacco)
  • Any contraindication to tACS
  • Major physical illness, neurological disorder, or traumatic brain injury that may affect the brain
  • Pregnant or breastfeeding women, or women planning pregnancy during the study

Read by machine on 12 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 50 years old?

Source: NCT07701343, who can take part

Where in China

  • The Second Xiangya Hospital of Central South UniversityChangsha, ChinaContact: Jimin ZhangTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Central South University
Trial code
NCT07701343
Record updated
28 October 2026
Original description
This study is a randomized, single-blind, sham-controlled crossover trial enrolling 30 schizophrenia patients, each receiving one active and one sham tACS session (7-day washout), targeting P3/P4 at individual alpha frequency (2mA, 30min) during a working memory task, with accuracy and reaction time as primary outcomes, alongside EEG and neurophysiological measures, to test the efficacy and mechanisms of individualized alpha-tACS on working memory.Read full original descriptionShow less

Efficacy and Mechanisms of Transcranial Alternating Current Stimulation in Improving Working Memory in Patients With Schizophrenia

This study is a randomized, single-blind, sham-controlled crossover trial enrolling 30 schizophrenia patients, each receiving one active and one sham tACS session (7-day washout), targeting P3/P4 at individual alpha frequency (2mA, 30min) during a working memory task, with accuracy and reaction time as primary outcomes, alongside EEG and neurophysiological measures, to test the efficacy and mechanisms of individualized alpha-tACS on working memory.

Inclusion: Aged 18-50 years, meeting the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnostic criteria for schizophrenia, confirmed by the Structured Clinical Interview for DSM-5 (SCID-5); Spatial span T-score <40 on the MATRICS Consensus Cognitive Battery (MCCB); Taking 1-2 antipsychotic medications, with stable dosage for at least 1 week prior to enrollment. No use of mood stabilizers, antidepressants, or excessive benzodiazepines (lorazepam equivalent >2 mg/day). The type and dosage of antipsychotic medications remain unchanged during the treatment period; Impaired functioning in daily activities; Willing to participate in this study and provide written informed consent.

Exclusion: Previously diagnosed with or comorbid any other DSM-5 mental disorder besides schizophrenia; Received other forms of electrical or magnetic stimulation therapy within 1 month prior to enrollment; Presence of significant mood symptoms or substance use disorder (other than caffeine and/or tobacco); History or current presence of any major physical illness, neurological disorder, or traumatic brain injury that may affect brain structure or function; Presence of any contraindication to transcranial alternating current stimulation (tACS); Pregnant or breastfeeding women, or women planning to become pregnant during the study period.

ClinicalTrials.gov NCT07701343