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Clinical Trials/KCT0005243
KCT0005243
Active, not recruiting
未知

Investigations of the effectiveness of computer-assisted cognitive intervention program for elderlies with cognitive decline

Gachon University0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Gachon University
Enrollment
60
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients with mild cognitive impairment according to Petersen's criteria (Petersen et al., 1999\) or mild neurocognitive disorder according to DSM\-5
  • 2\. Participants with subjective cognitive decline (Jessen et al. 2014\)
  • 3\. Age \= 60
  • 4\. MMSE \= 20
  • 5\. Individuals with no major lesion on Brain MRI such as intracranial haemorrhage, cerebral, cerebellar, or brainstem infarction, hydrocephalus, traumatic brain injury, severe white matter hyperintensity, tumours, multiple sclerosis, or vasculitis.
  • 6\. Individuals who voluntarily agreed to participate in the study

Exclusion Criteria

  • 1\. major psychiatric disorders such as major neurocognitive disorder, schizophrenia, bipolar disorder, and depressive disorder other than mild cognitive disorder and mild neurocognitive disorder
  • 2\. history of neurodegenerative disorders including Creutzfeldt\-Jakob disease, Pick’s disease, Huntington’s disease, Parkinson’s disease, inflammation associated with human immunodeficiency viruses, and syphilis
  • 3\. vascular major neurocognitive disorder according to DSM\-5
  • 4\. history of cerebral infarction within 1 year of the screening
  • 5\. participation of other clinical trial including pharmacotherapy within 3 months of the screening
  • 6\. participants who are not possible to undergo brain MRI or interview.
  • 7\. current major cancer including brain tumor
  • 8\. drug or medication abuser
  • 9\. Subjects deemed inappropriate by researchers to participate in the study

Outcomes

Primary Outcomes

Not specified

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