| Project/Area Number |
24591717
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Psychiatric science
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| Research Institution | Kagawa University |
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Principal Investigator |
NAKAMURA Yu 香川大学, 医学部, 教授 (70291440)
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| Co-Investigator(Kenkyū-buntansha) |
SHINNO Hideto 香川大学, 医学部, 客員教授 (10393430)
IMAI Hideki 香川大学, 医学部附属病院, 助教 (00558512)
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| Project Period (FY) |
2012-04-01 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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| Keywords | 認知症 / ADL / 全般臨床評価 / 抗認知症薬 / 介護者 / 臨床評価 |
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| Outline of Final Research Achievements |
To access the change of the clinical symptoms of AD patients, it is necessary to obtain much information of good quality from their caregivers. However, the information obtained from a single family caregiver has many problems. Then, we investigated where those problems are laying. It is concluded that it is necessary to get more information not only from a major caregiver but also from the other caregivers such as other family members and professional caregivers on the ADLs such as bathig, watching, excretion, short trip, dental care, dressing, taking medicines, leisure and house keeping.
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