JPRN-jRCTs012200016招募中未知
A study to investigate the neuronal mechanism of non-invasive brain stimulation and rehabilitation training in neurological disorders. - NIBS-RHB
Mukaino Masahiko0 个研究点目标入组 400 人开始时间: 2020年12月21日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 <= 90age old（—）
- 性别
- All
入选标准
- •Patients with neurological disorders
- •1. Nervous disease patients who have the following target diseases and whose diagnosis is established by neurological findings, image findings, etc.
- •target diseases:
- •Cerebrovascular disease (cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage etc.)
- •Neurodegenerative diseases (Parkinson's disease ,
- •Spinocerebellar degeneration etc.)
- •Neuroinflammatory disease (Multiple sclerosis etc.)
- •2. Patients who are suffering from any disorder due to neurological disorder, movement disorder, higher brain dysfunction, speech disorder, swallowing disorder.
- •3. Patients who received sufficient explanation to participate in this study and obtained document consent by the person's free will with sufficient understanding
- •4. Patients with movement disorders, higher brain dysfunction, speech disorders, or dysphagia due to neurological disorders
- •5. Patients who have received sufficient explanation before participating in this study, and who have obtained sufficient understanding and consent to the document at their own free will. Or, if it is difficult for the patient to consent to the document, the patient with the document consent obtained by the substitute
- •Healthy people
- •1. Those who are 20-90 years old at the time of obtaining consent
- •2. Those who have no history of neuropsychiatric illness in their declaration.
- •3. Persons who have received sufficient explanation before participating in this study, and who have obtained sufficient understanding and consent to the document at their own free will.
排除标准
- •Patients with neurological disorders
- •1. Within 5 days after onset or within 5 days after symptom recurrence
- •2. Those who have significant hearing impairment and cannot communicate
- •3. Those who have a cardiac pacemaker
- •4. Those who are holding a body-metal that cannot be confirmed to be a non-magnetic material (aneurysm clip, mechanical artificial valve, nerve stimulator, insulin pump, intraocular metal, etc.)
- •5. Those who are judged by the principal investigator to be inappropriate as research subjects
- •Healthy people
- •1. Those who have significant hearing impairment and cannot communicate
- •2. Those who have a cardiac pacemaker
- •3. Those who are holding a body-metal that cannot be confirmed to be non-magnetic (aneurysm clip, mechanical artificial valve, nerve stimulator, insulin pump, intraocular metal, etc.)
- •4. Those who are judged by the principal investigator to be inappropriate as research subjects
研究者
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