Home-based Cognitive Monitoring in MCI

Status Recruiting

Clinical Trial Summary

This study is an observational study to confirm usefulness of a home-based cognitive monitoring in non-demented patients with high-risk of dementia

Clinical Trial Description

We prospectively enroll subjects who were diagnosed as mild cognitive impairment based on neuropsychological tests battery, brain MRI, and routine blood labs including thyroid function tests, vitamine B12 & folate levels, and syphilis screening to rule out other secondary causes of dementia. We undergo peripheral blood-based amyloid beta levels and regular home-based cognitive monitoring (every 3 months) to investigate whether amyloid-positive MCIs progress rapidly using home-based cognitive monitoring during 6 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04350801
Study type	Observational
Source	Asan Medical Center
Contact	YunJeong Hong, MD,PhD
Phone	820318203933
Email	hyj2009@hanmail.net
Status	Recruiting
Phase
Start date	December 1, 2019
Completion date	December 30, 2020

View Details

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