Cognitive Function Training Using Smartphone Applications for Patients with Mild Cognitive Impairment

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008311

Enrollment

Registered

2023-03-22

Start date

2022-12-02

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 1:1:1 to multidomain intervention group and sharm control/waitlist control group. Random assignment is randomly assigned 1:1:1 using a random number table generated by Excel.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: A) Adult men and women aged 18 years or older B) Patients or guardians complain of memory loss C) Through neuropsychological tests, cognitive ability, including memory, is reduced compared to age and education level. D) Maintain overall cognitive function E) No hindrance to daily life F) It should not be dementia according to the judgment of the clinician G) Subjects or their legal representatives voluntarily decide to participate in the study and give written consent after listening to a detailed explanation of this study and fully understanding it

Exclusion criteria

Exclusion criteria: a) any advanced, severe, progressive or unstable disease that could put the patient at risk; B) Any medical or other neurological disease that can explain cognitive decline (e.g., abnormal thyroid function test, vitamin B12 or folic acid deficiency, post-traumatic disease, Huntington's disease, multiple sclerosis, cerebral palsy, encephalitis, meningitis, etc. - diseases affecting the central nervous system) c) any other DSM-V Axis I diagnosis, including primary neurodegenerative dementia other than depression, schizophrenia, or bipolar disorder D) Those who currently have uncontrolled convulsive disease E) A person who has a history of loss of consciousness for more than 1 hour or a brain injury accident that resulted in hospitalization within 3 years F) Hearing or vision impairment that may interfere with the performance of the requirements of the clinical trial G) Those who are judged not to be suitable for research according to the judgment of the researcher

Design outcomes

Primary

Measure	Time frame
ADAS-Cog 13 total points	—

Secondary

Measure	Time frame
ADAS-Cog 13 score by domain, ADCS-ADL-MCI score , K-MMSE 2, CDR, GDeS	—

Countries

Korea, Republic of

Contacts

Public ContactHayeong Choi

Hallym University Medical Center- Chuncheon

hy_choi@kangwon.ac.kr+82-33-240-5000

Outcome results