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Effectiveness for lifestle modification in mild cognitive disorders by using digital health service

Effectiveness for lifestle modification in mild cognitive disorders by using digital health service

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008315
Enrollment
96
Registered
2023-03-22
Start date
2020-10-28
Completion date
Unknown
Last updated
2023-04-04

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

Conditions

None listed

Interventions

Behavioral : Allocate 1:1 to multidomain intervention/control group. Random assignment is performed 1:1 by performing random assignment (block Randomization) for each group using a random number table

Sponsors

Hallym University Medical Center- Chuncheon
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age: over 40 years old 2. The patient or guardian complains of cognitive impairment 3. A selective neuropsychological test confirmed that cognitive function including memory decreased compared to age and education years 4. No hindrance to daily life 5. Must not have dementia according to the judgment of the clinician. 6. Subjects or their legal representatives voluntarily decide to participate in the study and give written consent after listening to a detailed explanation of the study and fully understanding it

Exclusion criteria

Exclusion criteria: 1. Subjects who have been found to have neurological abnormalities that may cause memory impairment through medical examination 2. Those with a history of Axis 1 psychiatric disorders including past intellectual disability, schizophrenia, alcoholism, and bipolar disorder 3. Those who have undergone cerebrovascular surgery such as brain surgery or carotid artery surgery 4. Those with neurological symptoms that are evidence of cerebrovascular disease 5. A person with a history of loss of consciousness for more than 1 hour or a brain injury accident that resulted in hospitalization 6. Those who currently have the uncontrolled convulsive disease 7. Any advanced severe, progressive, or unstable disease that could put the patient at risk 8. Hearing or vision impairment that may interfere with the performance of the requirements of the clinical trial 9. A person who is judged not suitable for research according to the judgment of the researcher

Design outcomes

Primary

MeasureTime frame
CERAD test total score

Secondary

MeasureTime frame
CERAD Subcategory Score, MMSE-DS, CDR sum of boxes, CGI, NPI, GDeS

Countries

Korea, Republic of

Contacts

Public ContactHayeong Choi

Hallym University Medical Center- Chuncheon

hy_choi@kangwon.ac.kr+82-33-240-5174

Outcome results

None listed

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