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A Study on the Application of Standard Clinical Pathways of Korean Medicine in Neurocognitive Disorders

A Prospective Observational Study on the Application of Standard Clinical Pathways of Korean Medicine in Neurocognitive Disorders

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0009952
Enrollment
30
Registered
2024-11-27
Start date
2024-10-14
Completion date
Unknown
Last updated
2024-12-09

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

Daejeon Korean Medicine Hospital of Daejeon University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Men and women aged 50 to 85 2) Clinically diagnosed with Alzheimer's disease, a major neurocognitive disorder due to vascular disease, or mild neurocognitive disorder (based on DSM-5 criteria) 3) Participants who have provided written consent themselves or through their legal representative for clinical research

Exclusion criteria

Exclusion criteria: 1) Individuals with cognitive impairment due to neurodegenerative diseases such as Parkinson's disease, Huntington's disease, frontotemporal dementia (FTD), or Creutzfeldt-Jakob disease. 2) Individuals with a history of systemic diseases that lead to dementia, including but not limited to hypothyroidism, vitamin B12 or folic acid deficiency, niacin deficiency, neurosyphilis, or HIV-related neurocognitive disorders known to cause or contribute to cognitive decline. 3) Individuals with a history of major mental illnesses diagnosed under DSM-5, including but not limited to schizophrenia, delusional disorder, bipolar disorder, or substance-related disorders (including alcohol and other substances). 4) Individuals with a history of neurological disorders such as epilepsy, focal brain damage, or head trauma. 5) Individuals with gastrointestinal, endocrine, or cardiovascular diseases that are difficult to manage or not adequately controlled through diet or medication. 6) Individuals deemed to be in a serious and unstable health condition by the attending clinician, based on clinical pathology tests, electrocardiogram (EKG) results, chest X-ray, vital signs, and other related medical evaluations. 7) Individuals considered unsuitable for participation in this clinical study according to the researcher’s judgment.

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment-Korean version(MoCA-K);Korean-Dementia Rating Scale(K-DRS)

Secondary

MeasureTime frame
Heart Rate Variability (HRV);Clinical Dementia Rating Scale(CDR);Global Deterioration Scale(GDS);Short-form Geriatric Depression Scale(SGDS);Korean version of Instrumental Activity of Daily Living(K-IADL);Neuropsychiatric Inventory–Questionnaire(NPI-Q);Pattern Identifications Tool for Cognitive Disorders(PIT-C);The 5-level EuroQol-5 Dimension(EQ-5D-5L);Clinical pathway applicability indicators

Countries

Korea, Republic of

Contacts

Public ContactMira Hur

Daejeon Korean Medicine Hospital of Daejeon University

relaxom9@dju.kr+82-42-470-9544

Outcome results

None listed

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