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

Not Applicable

Completed

• Conditions: Mental and behavioural disorders

• Registration Number: KCT0008315
• Lead Sponsor: Hallym University Medical Center- Chuncheon

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-02-28
• Last Update Posted: 4 April 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 96

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

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

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
CERAD test total score

Secondary Outcome Measures

Name	Time	Method
CERAD Subcategory Score, MMSE-DS, CDR sum of boxes, CGI, NPI, GDeS