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Cognitive Behavioral Therapy for people with mild cognitive impairment, mild dementia and the family-caregiver in Japan.

Not Applicable
Conditions
mild dementia, and mild cognitive impairment
Registration Number
JPRN-UMIN000022297
Lead Sponsor
ippon Medical School
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

CBT for patient 1. Less than 19 points of HDS-R and MMSE. 2. Patients who cannot continue the intervention due to concurrent psychiatric disorders (ex. schizophrenia, bipolar disorder, alcohol / drug related disorder, A cluster personality disorder, etc.) 3. Patients who have a history of epilepsy and whose EEG has not been normalized. 4. Patients who have too severe cognitive dysfunctions to do CBT sessions. 5. Physical disease that may interfere psychological treatment. 6. Patients who have already received CBT or currently receive it. 7. Patients who are judged by the principal investigator due to other reasons, such as difficulty in understanding the procedure of the study or intervention protocol due to illiteracy or intellectual problem, and etc. CBT for family-caregiver 1. With a history of any physical diseases that may interfere psychological treatment and any psychiatric disorders, such as . schizophrenia, bipolar disorder, alcohol / drug related disorder, A cluster personality disorder, etc. 2. People who are given one month to live due to any severe physical diseases. 3. Expected difficult cases, due to having a full schedule, lack motivation, illiteracy, or severe cognitive disorder. 4. People who having a structured psychological therapy (except for supportive therapy). 5. People who are judged by the principal investigator due to other reasons, such as in pregnancy, difficulty in understanding the procedure of the study or intervention protocol due to illiteracy or intellectual problem, and etc.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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