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Home-based Cognitive Monitoring in MCI

Usefulness of a Home-based Cognitive Monitoring in Non-demented Patients With High-risk of Dementia: a Prospective Observational Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04350801
Enrollment
40
Registered
2020-04-17
Start date
2019-12-01
Completion date
2020-12-30
Last updated
2020-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Impairment

Keywords

mild cognitive impairment, blood amyloid beta, home-based cognitive monitoring

Brief 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

Detailed 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.

Interventions

DIAGNOSTIC_TESThome-based cognitive monitoring

a newly developed home-based cognitive monitoring (about 3-5 minutes per test; total score ranges from 0\ 30; higher score indicates better cognition)

Sponsors

Asan Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* persistent cognitive complaints * aged 50 years old or older * below -1.0 standard deviation in any domain of detailed neuropsychological tests battery named SNSB (Seoul neuropsychological screening battery) * no ADL (activities of daily living) limitation * subjects who agreed to participate

Exclusion criteria

* dementia patients * other structural brain disorders such as hydrocephalus, hemorrhage, or tumors * other neurological disease such as Huntington's disease, Parkinson's disease, or epilepsy

Design outcomes

Primary

MeasureTime frameDescription
home-based cognitive monitoring score3 months (at baseline, 3 months from baseline, 6 months from baseline)a 3-5 minutes brief cognitive testing (range 0\ 30, higher score means better outcome) using telephone

Secondary

MeasureTime frameDescription
Hippocampal atrophy gradeat baselinebaseline brain MRI markers for hippocampal atrophy using Scheltens' visual rating scale (range 0\ 4, higher score means more hippocampal atrophy)
Number of lacunesat baselinenumber of lacunes using manual counting on brain MRI (no limit)
Number of microbleedsat baselinenumber of microbleeds using manual counting on brain MRI (no limit)

Countries

South Korea

Contacts

Primary ContactYunJeong Hong, MD,PhD
hyj2009@hanmail.net820318203933

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026