KCT0009281
已完成
未知
The effectiveness of computerized cognitive training program for older adults with mild cognitive impairment and early dementia
概览
- 阶段
- 未知
- 干预措施
- 未指定
- 疾病 / 适应症
- 未指定
- 发起方
- Gachon University Gil Medical Center
- 入组人数
- 70
- 状态
- 已完成
- 最后更新
- 2年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •1\. Subjects diagnosed with mild cognitive impairment according to Petersen’s criteria (Petersen et al., 1999\) or early stage of major neurocognitive disorder according to DSM\-5 (American Psychiatric Association, 2013\)
- •2\. Korean male or female over 60 years of age
- •3\. Subjects with Clinical dementia rating global scale \= 1
- •4\. Subjects whose existing treatment (medication or face\-to\-face treatment) can be confirmed (existing treatment itself is irrelevant)
- •5\. Subjects for whom no other structural causes of cognitive decline were found in brain MRI
- •6\. After hearing and fully understanding the detailed explanation of this clinical trial, the subject voluntarily decided to participate and signed the consent form to comply with the precautions.
排除标准
- •1\. Subjects with mental illness other than mild cognitive impairment and early Alzheimer's disease (schizophrenia, bipolar disorder, depression, etc.)
- •2\. Subjects diagnosed with or accompanied by cognitive decline due to other degenerative brain diseases, infections of the central nervous system (HIV, syphilis, etc.), head trauma, Creutzfeld\-Jacob disease, Pick's disease, Huntington's disease, and Parkinson's disease
- •3\. Subjects diagnosed with vascular dementia according to DSM\-5 (American Psychiatric Association, 2013\) criteria
- •4\. Subjects with a history of stroke within 1 year of participating in the trial
- •5\. Subjects who have participated in other treatment studies, including drugs, within 3 months before the start of the clinical trial (week 0\)
- •6\. Those who cannot undergo tests (e.g. fMRI) conducted during the clinical trial period
- •7\. Cancer patients (systemic cancer including brain tumor)
- •8\. Drug/alcohol abuser
- •9\. Other subjects deemed unsuitable by researchers to participate in clinical trials
结局指标
主要结局
未指定
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