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Establishment of registry to apply dementia integrative medical service model

Establishment of registry to apply dementia integrative medical service model

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0009174
Enrollment
40
Registered
2024-02-15
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

None listed

Interventions

None listed

Sponsors

Wonkwang University Jangheung Integrative Medical Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult men and women aged 55 to 90 years old 2) Those diagnosed with major neurocognitive disorder due to Alzheimer's disease or major neurocognitive disorder due to vascular disease according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) 3) A person who decides to participate voluntarily or through the will of a legal representative and signs a consent form

Exclusion criteria

Exclusion criteria: - patient 1) Those with a history of malignant tumor within 5 years of the screening visit 2) People with dementia caused by causes other than Alzheimer's disease or vascular dementia, that is, degenerative brain diseases such as Parkinson's disease, Huntington's disease, frontotemporal dementia, Creutzfeldt-Jakob disease, etc. 3) Those with systemic conditions that cause dementia, such as hypothyroidism, vitamin B12 or folic acid deficiency, niacin deficiency, hyperkalemia, neurosyphilis, human immunodeficiency virus disease, etc. 4) Those with a history of major psychiatric disorders diagnosed by DSM-5, such as schizophrenia, delusional disorder, depression, bipolar disorder, alcohol or substance abuse disorder, etc. 5) Those with a history of neurological disorders such as epilepsy, focal brain damage, or head trauma 6) People with gastrointestinal, endocrine and cardiovascular diseases that cannot be controlled by diet or drug treatment 7) Persons with a seriously unstable medical condition (based on the judgment of the attending physician based on the results of clinical laboratory tests, electrocardiogram tests, chest x-rays, vital signs, etc.) 8) Those who participated in another clinical trial within 3 months before the start of the study 9) Those who are not suitable for participation in this clinical trial according to the judgment of the researcher

Design outcomes

Primary

MeasureTime frame
GQOL-D

Secondary

MeasureTime frame
Cognitive evaluation, daily living ability evaluation, neuropsychiatric behavior test, depression-related test, quality of life scale(MMSE, GDS, S-GDpS, NPI-Q, Barthel-ADL, S-IADL, EQ-5D, EQ-VAS, HRV );Economic evaluation;Safety evaluation(Adverse effect)

Countries

Korea, Republic of

Contacts

Public ContactDoeun Lee

Wonkwang University

dolee0210@gmail.com+82-61-860-7777

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026