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临床试验/NCT06231732
NCT06231732招募中不适用

The Impact of High-frequency Transcranial Alternating Current Stimulation (Hi-tACS) on Cognitive Function in Patients With Schizophrenia: a Pilot Study

Sir Run Run Shaw Hospital1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2023年11月14日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
12
试验地点
1
主要终点
functional near-infrared spectroscopy

研究概览

简要总结

This study is a double-blind, randomized, controlled intervention study aimed at exploring whether high-frequency transcranial alternating current stimulation (Hi-tACS) can improve cognitive impairment in patients with schizophrenia.

详细描述

Schizophrenia is a chronic, severe mental disorder characterized by a high suicide rate and significant disability. Cognitive impairment is one of the core symptoms of schizophrenia, with approximately 98% of patients experiencing a decline in cognitive function compared to pre-illness levels. Research has found that individuals with schizophrenia show significant impairments in seven domains, including reaction time, attention, working memory, verbal learning and memory, visual learning and memory, logical reasoning, and social cognition.

Pharmacological treatment remains the primary approach for managing schizophrenia. However, cognitive impairment in individuals with schizophrenia often does not respond well to medication. Additionally, electroconvulsive therapy (ECT) may have potential cognitive side effects. Transcranial alternating current stimulation (tACS), a form of noninvasive brain stimulation, has been found in several studies to improve cognition. However, its effectiveness is not yet clear.

Conventional tACS utilizes weak currents below 4mA, which can only directly stimulate certain cortical areas and indirectly stimulate deep brain structures. Moreover, the targeting of specific brain regions can be complex, and users may experience a sensation of heat on the skin where the electrodes come into contact.High-frequency transcranial alternating current stimulation (Hi-tACS) employs electrical currents greater than 10mA, typically ranging from 10-15mA. Unlike conventional tACS, Hi-tACS can apply stimulation to the entire brain, potentially enhancing its therapeutic effects. Moreover, Hi-tACS does not require precise targeting and is generally well-tolerated without any discomfort during the stimulation. It is considered a promising and potentially safe treatment modality for cognitive impairment in schizophrenia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Meets the diagnostic criteria for schizophrenia according to DSM-
  • Age ≥ 18 years old.
  • Right-handed.
  • Willing to participate in this study and sign an informed consent form. If the participant is unable to read and sign the informed consent form due to lack of capacity, a legal guardian must act as a proxy during the informed consent process and sign the form.
  • Clinically stable, receiving antipsychotic medication treatment with a stable dose for 4 weeks without any changes.
  • Montreal Cognitive Assessment score ≥ 10 points.

排除标准

  • Psychotic disorders caused by split affective disorder, bipolar disorder, intellectual disability, anxiety spectrum disorders, drugs, alcohol, and other psychoactive substances according to DSM-V diagnostic criteria.
  • Those with severe or unstable organic diseases, with a history of brain tumors or epilepsy.
  • Those who have received MECT or TMS treatment within 1 month before enrollment.
  • Skin integrity at the electrode placement site is compromised. Allergy to electrode gel or adhesive.
  • Implants of metal or electronic devices (such as pacemakers, cochlear implants, deep brain stimulators, aneurysm clips, internal fixation devices after ventriculoperitoneal shunt surgery, etc.).
  • Participation in any other clinical trials within 1 month prior to baseline.
  • Pregnant and lactating women.
  • The investigator believes that there are inappropriate conditions for participating in this study.

结局指标

主要结局

functional near-infrared spectroscopy

时间窗: 30 days of treatment

Functional near-infrared spectroscopy (fNIRS) measures the oxygen content of the cerebral cortex and provides the values of oxy-emoglobin and deoxygenatedhemoglobin in real time, indicating the level of brain activity

scores of Repeatable Battery for the Assessment of Neuropsychological Status

时间窗: 30 days of treatment

The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) is a standardized cognitive assessment tool used in clinical and research settings. It evaluates cognitive abilities such as attention, memory, language, and visuospatial skills. The RBANS consists of 12 subtests and takes about 45-60 minutes to complete. It is efficient, providing a comprehensive assessment of cognitive functioning. The RBANS is extensively validated and normed, making it reliable for assessing cognitive performance. It provides standardized scores for comparison with peers, making it useful for detecting cognitive impairments. Overall, the RBANS is a valuable tool for evaluating cognitive functioning and tracking changes over time.

次要结局

  • scores of Positive and Negative Syndrome Scale(One day before the start of the treatment, 10 days of treatment, 30 days of treatment)
  • scores of Montreal Cognitive Assessment Scale(One day before the start of the treatment, 10 days of treatment, 30 days of treatment)
  • scores of Hamilton Anxiety Scale(One day before the start of the treatment, 10 days of treatment, 30 days of treatment)
  • scores of Auditory Hallucinations Rating Scale(One day before the start of the treatment, 10 days of treatment, 30 days of treatment)
  • scores of Hamilton Depression Scale(One day before the start of the treatment, 10 days of treatment, 30 days of treatment)
  • scores of Pittsburgh sleep quality index(One day before the start of the treatment, 10 days of treatment, 30 days of treatment)
  • The Clinical Assessment Interview for Negative Symptoms(One day before the start of the treatment, 10 days of treatment, 30 days of treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jinsong Tang

Deputy chief physician

Sir Run Run Shaw Hospital

研究点 (1)

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