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Shanghai Mild Cognitive Impairment Cohort Study

Completed
Conditions
Mild Cognitive Impairment
Registration Number
NCT01552265
Lead Sponsor
Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan
Brief Summary

This study was planned 1) to identify individuals with Mild Cognitive Impairment (MCI) who convert to Alzheimer's Disease (AD), and 2) to explore factors associated with the conversion.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
400
Inclusion Criteria
  1. Cognitive concern reflecting a change in cognition reported by the patient or informant or clinician
  2. Mini-Mental State Examination (MMSE) scores between 18-30 (inclusive)
  3. Clinical Dementia Rating (CDR) =0.5; Memory Box score must be at least 0.5
  4. Objective memory loss* as evidenced by Auditory Verbal Learning test (AVLT-HS)
  5. Essentially preserved activities of daily living based on Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL)
  6. Not-demented, as defined by '"All-cause Dementia" (see 3.4. All-cause Dementia)
  7. Willing to and able to undergo all test procedures including neuroimaging, and agree to longitudinal follow up
  8. Written informed consent for the participation of this study including repeated neuropsychological tests and MRI scans
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to Conversion from MCI to "Probable AD Dementia"3 years
Secondary Outcome Measures
NameTimeMethod
Changes in Neuropsychological examinationsbaseline, annual and 3 years
Time to Conversion from MCI to "Possible AD Dementia" or "Probable AD Dementia"3 years
Overall survival3 years
Changes in MRIbaseline, annual and 3 years
Time to Conversion from MCI to "All-cause Dementia"3 years

Trial Locations

Locations (1)

Department of Neurology, Huashan Hospital, Fudan University

🇨🇳

Shanghai, Shanghai, China

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