Assessment of Brain Activity Change in Computerized Cognitive Rehabilitation Program in the Elderly between dementia and healthy

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0003328

Enrollment

Registered

2018-11-09

Start date

2018-09-12

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Others(Computerized Cognitive Rehabilitation Program) : &lt

cognitive impairment group &gt

The cognitive impairment group receives a total of 20 computerized cognitive rehabilitation treatments for 30 minutes and 5 times a week for 4 weeks using a tablet version of the computerized cognitiv

Better Cog&quot

. &lt

Normal control group&gt

The normal control group does not receive treatment.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: <Common> 1.Adults over 65 <Cognitive Impairment Group> 1. Subjects with K-MMSE(Korea-Mini Mental Stare Examination) score less than 24 2. Subjects between CDR 0.5-2 points, mild cognitive impairment and mild / moderate dementia <Normal control group> 1. Subjects with K-MMSE(Korea-Mini Mental Stare Examination) score more than 24 2. Subjects between CDR 0-0.5 points, normal and mild cognitive impairment *CDR 0.5 Dementia suspects are classified as mild cognitive impairment according to SNSB(Seoul-Neuropsychological Screening Battery) scores. If one or more of the five domains of the SNSB %ile score is less than 15%ile, it is classified as a mild cognitive disorder.

Exclusion criteria

Exclusion criteria: 1.Subjects with Hearing impairment 2.Subjects with visual impairment 3.Subjects with Claustrophobia 4.Subjects with a history of brain surgery 5.Severe dementia with a CDR of 2 points or more 6.Moderate to severe aphasia 7.Mental illnesses other than dementia 8.Subjects with trembling due to Parkinson's disease and other diseases 9. Subjects with nervous or musculoskeletal disorders that can not operate the touch screen by themselves 10.Subjects who have started taking medications for dementia within the last 3 months or who have changed their medication 11. Subjects who can not take MRI due to a medical device implanted in the body, such as artificial heartbeat, cerebrovascular surgery

Design outcomes

Primary

Measure	Time frame
Seoul Neuropsychological Screening Battery;Korea Mini Mental State Examination;Clinical Dementia Rating;Change of Brain blood flow (by NIRS);Change of Brain activity (by fMRI)	—

Secondary

Measure	Time frame
Barthel-ADL;K-IADL	—

Countries

Korea, Republic of

Contacts

Public ContactYOO SU WON

Chungbuk National University Hospital

sw1181@naver.com+82-43-269-8706

Outcome results