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临床试验/NCT04135742
NCT04135742Unknown不适用

Effects of Transcranial Alternating Current Stimulation(tACS) Combined With Computerized Cognitive Training for Patients With Mild Cognitive Impairment(MCI)

Shanghai Mental Health Center2 个研究点 分布在 1 个国家目标入组 195 人开始时间: 2019年11月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
195
试验地点
2
主要终点
Change from baseline RBANS, Color Word Stroop Test (CWST),Visual Reasoning and Trails Making Task.

研究概览

简要总结

This goal of this study is to explore the effects of transcranial alternating current stimulation(tACS) combined with computerized cognitive training(CCT) on improving cognition for patients with mild cognitive impairment(MCI). The study will recruit 195 patients with MCI. Participants will undergo baseline cognitve assessment, EEG and structural and functional MRI. Participants will be randomized to active tACS+CCT group, sham tACS+CCT group and active tACS+sham CCT group. At the end of the intervention, 3-month, 6-month and 12-month follow-up, all subjects will repeat the baseline assessments.

详细描述

tACS is a non-invasive brain stimulation technique that uses a low-intensity alternating current (1 to 2 mA) to apply a sinusoidal current to the scalp, directly interacting with the oscillating cortical activity at a given frequency with a given stimulus intensity. Studies have shown that simultaneous tACS on the left prefrontal lobe and left temporal lobe can significantly improve working memory in healthy older adults. The 40 Hz tACS is gamma oscillation, and more and more studies have pointed out that gamma oscillation regulation disorder is associated with impaired working memory function.CCT can improve the cognition in patients with MCI. We hypothesized that tACS combined with CCT can produce synergistic effects in sensitive brain areas.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
60 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •(1)age ≥ 60 years old with memory impairment; (2) the memory test scores are lower 1.5 SD than the normal control; (3) in addition to memory impairment, other cognitive functions remain relatively intact or only slightly impaired; (4) normal daily living ability; (5) can not reach the diagnostic criteria for dementia, Clinical Dementia Rating (CDR) is 0.5

排除标准

  • •(1) serious medical diseases such as hypertension, heart disease, severe liver disease, etc.; (2) central nervous system diseases such as cerebrovascular diseases, infectious encephalopathy, brain tumors, etc.; (3) severe depression, schizophrenia and patients who have taken psychotropic substances for a long time; (4) Alzheimer's disease and vascular dementia; (5) history of alcohol dependence and other psychoactive substance abuse; (6) patients with contraindications for magnetic resonance imaging; (7) cannot complete the cognitive function tests for various conditions

研究组 & 干预措施

active tACS+ Cognitive Training group

Experimental

Subjects will receive CCT for a period of 3 months, 24 times, twice a week for 20 minutes each time.

Placement of stimuli electrodes will be: a) active electrode over the left DLPFC (F3), and b) reference electrode over the right parietal region (P4). The exact location of electrodes will be determined by the 10/20 EEG method with EEG cap. Subjects will have 24 tACS sessions for three months, twice a week.The active tACS group will be stimulated with a 2 mA,40Hz current for 20 minutes each time during the stimulation.

干预措施: Transcranial Alternating Current Stimulation (Device)

active tACS+ Cognitive Training group

Experimental

Subjects will receive CCT for a period of 3 months, 24 times, twice a week for 20 minutes each time.

Placement of stimuli electrodes will be: a) active electrode over the left DLPFC (F3), and b) reference electrode over the right parietal region (P4). The exact location of electrodes will be determined by the 10/20 EEG method with EEG cap. Subjects will have 24 tACS sessions for three months, twice a week.The active tACS group will be stimulated with a 2 mA,40Hz current for 20 minutes each time during the stimulation.

干预措施: Cognitive Training (Behavioral)

sham tACS+Cognitive Training group

Sham Comparator

Subjects will receive CCT for a period of 3 months, 24 times, twice a week for 20 minutes each time.

Placement of stimuli electrodes will be: a) active electrode over the left DLPFC (F3), and b) reference electrode over the right parietal region (P4). The exact location of electrodes will be determined by the 10/20 EEG method with EEG cap. Subjects will have 24 tACS sessions for three months, twice a week.The sham tACS group will have stimulation lasting only 40 seconds though the electrodes will remain in place for 20 min.

干预措施: Cognitive Training (Behavioral)

active tACS+ sham Cognitive Training group

Sham Comparator

Subjects will watch neutral pictures on iPad for a period of 3 months, 24 times, twice a week for 20 minutes each time.

Placement of stimuli electrodes will be: a) active electrode over the left DLPFC (F3), and b) reference electrode over the right parietal region (P4). The exact location of electrodes will be determined by the 10/20 EEG method with EEG cap. Subjects will have 24 tACS sessions for three months, twice a week.The active tACS group will be stimulated with a 2 mA,40Hz current for 20 minutes each time during the stimulation.

干预措施: Transcranial Alternating Current Stimulation (Device)

结局指标

主要结局

Change from baseline RBANS, Color Word Stroop Test (CWST),Visual Reasoning and Trails Making Task.

时间窗: up to 3 months(end of the intervention)

Global cognition will be assessed by the Repeatable Battery for the Assessment of Neuropsychological Status Total Score (RBANS).CWST mainly can examine the executive function. Visual Reasoning will be assessed by the Cambridge Mental Disorders of the Elderly Examination Visual Reasoning Test.Executive function will be assessed by Trails Making Task.

Neuroimage change from baseline Magnetic Resonance Imaging (MRI)

时间窗: up to 3 months(end of the intervention)

Including T1, resting state functional MRI, task based functional MRI and Diffusion Tensor Imaging(DTI)

changes in Gamma oscillation intensity (40-80 Hz) over DLPFC

时间窗: up to 3 months(end of the intervention)

measured by electroencephalogram (EEG)

次要结局

  • Neuroimage changes from baseline Magnetic Resonance Imaging (MRI)(6 months after the end of the intervention and 12 month after the end of the intervention)
  • Side-effects of tACS(At each stimulation session,up to 3 months.)
  • Changes from baseline RBANS(3 months after the end of the intervention,6 months after the end of the intervention and 12 month after the end of the intervention)
  • Changes from baseline Visual Reasoning(3 months after the end of the intervention,6 months after the end of the intervention and 12 month after the end of the intervention)
  • Changes from baseline in Geriatric Anxiety Inventory (GAI)(up to 3 months(end of the intervention),3 months after the end of the intervention,6 months after the end of the intervention and 12 month after the end of the intervention)
  • Changes from baseline Color Word Stroop Test (CWST)(3 months after the end of the intervention,6 months after the end of the intervention and 12 month after the end of the intervention)
  • Changes from baseline Trails Making Task(3 months after the end of the intervention,6 months after the end of the intervention and 12 month after the end of the intervention)
  • Changes from baseline Geriatric Depression Scale (GDS)(up to 3 months(end of the intervention),3 months after the end of the intervention,6 months after the end of the intervention and 12 month after the end of the intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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