KCT0008861
Not yet recruiting
未知
A randomized, prospective single center clinical trial to compare the cognitive improvement effects of electroacupuncture and computerized cognitive rehabilitation for mild cognitive impairment
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Dongshin University
- Enrollment
- 64
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. an elderly aged between 55 and 85 years
- •2\. impaired memory lasting for at least 3 months meeting the diagnostic criteria for MCI
- •3\. Global Deterioration scale score of 2 or 3
- •4\. Korean version of Mini\-Mental State Examination(K\-MMSE) score of 20–23
- •5\. Korean version of Montreal Cognitive Assessment scale (MoCA\-K) score of 0\-22
- •6\. Geriatric Depression Scale (GDS) score of 0\-18
- •7\. at least six years of education or adequate Korean language proficiency for reliable study assessments
- •8\. voluntary provision of informed consent.
Exclusion Criteria
- •1\. Diagnosis of vascular dementia according to the NINDS\-AIREN criteria or diagnosis of AD according to the NINCDS\-ADRDA criteria
- •2\. a history of structural brain lesions that could cause cognitive decline, such as congenital mental retardation, stroke, traumatic brain injury, or intracranial space\-occupying lesions
- •3\. presence of a serious illness (e.g., Huntington disease, Parkinson's disease, cancer, central nervous system, liver, cardiovascular, and kidney diseases, and multiple sclerosis)
- •4\. a history of brain diseases confirmed on brain magnetic resonance imaging or computed tomography within 12 months
- •5\. history of treatment for drug or alcohol dependency or mental illness (schizophrenia, serious anxiety, or depression) within 6 months prior to screening
- •6\.current treatment for MCI, such as Korean medicine treatment, medication, or cognitive training within 4 weeks before screening
- •7\. difficulties in undergoing outcome measurement due to visual and hearing impairments
- •8\. unfitness for electroacupuncture (e.g., blood\-clotting abnormalities such as hemophilia, scalp infection, and presence of a pacemaker)
- •9\. pregnancy or breastfeeding
- •10\. A people who is participating in other trials or has participated in other trials within 8 weeks prior to screening
Outcomes
Primary Outcomes
Not specified
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