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A Genetic Study for Alzheimer Dementia: Case-control Study

A Genetic Study for Alzheimer Dementia: Case-control Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06330155
Enrollment
20
Registered
2024-03-26
Start date
2024-03-26
Completion date
2026-12-31
Last updated
2024-04-04

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

Conditions

Alzheimer Dementia (AD)

Brief summary

The purpose of this study is to find out the difference in genetic test results between Alzheimer's dementia patients and healthy subjects. The investigators want to identify genes that are importantly related to Alzheimer's dementia.

Interventions

None listed

Sponsors

MinYoung Kim, MD, PhD
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Inclusion Criteria: Alzheimer's dementia patient * Adult patients over 60 years old * Patients with a Alzheimer's dementia patient * Total Korean version of mini-mental state examination (K-MMSE) score less than 24 * Total Clinical Dementia Rating (CDR) over 0.5 2. Inclusion Criteria: healthy subjects * Adult healthy over 60 years old * Total Korean version of mini-mental state examination (K-MMSE) over 24 * Total Clinical Dementia Rating (CDR) is 0 3.

Exclusion criteria

* Those with severe medical conditions such as unstable conditions of the cardiovascular system, digestive system, respiratory system, endocrine system, etc., who are in poor general condition * In the case of a person with impaired consent (MMSE less than 10 points), if not accompanied by a guardian * Other cases where the researcher determines that participation in this clinical trial is not appropriate (Patients who are participating in other studies or have participated in other studies within the past 30 days can also participate in this study.)

Design outcomes

Primary

MeasureTime frameDescription
genetic analysisBaseline5cc blood collection for genetic testing

Secondary

MeasureTime frameDescription
Measurement of Korean version of mini-mental state examination (K-MMSE)screening, BaselineK-MMSE is a measurement of cognitive level. Any score of 24 or more (out of 30) indicates a normal cognition. Below this, scores can indicate severe(≤9 points), moderate (10-18 points) or mild (19-23 points) cognitive impairment(MCI). The raw score may also need to be corrected for educational attainment and age.
Measurement of Clinical Dementia Rating (CDR)screening, BaselineCDR is a rating scale for staging patients diagnosed with dementia. The CDR evaluates cognitive, behavioral and functional aspects of Alzheimer disease and other dementias. It is calculated on the basis of testing six different cognitive and behavioral domains such as memory, orientation, judgment and problem solving, community affairs, home and hobbies performance, and personal care. The CDR is based on a scale of 0-3: no dementia (CDR = 0), questionable dementia (CDR = 0.5), MCI (CDR = 1), moderate cognitive impairment (CDR = 2) and severe cognitive impairment (CDR = 3)
Measurement of Geriatric Depression Scale (GDSd)BaselineGDS is a 30-item self-report assessment used to identify depression in the elderly. One point is assigned to each answer and the cumulative score is rated on a scoring grid. The grid sets a range of 0-9 as normal, 10-19 as mildly depressed, and 20-30 as severely depressed.

Contacts

Primary ContactMinYoung Kim, MD, PhD
kmin@cha.ac.kr82-31-780-6281

Outcome results

None listed

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