| Project/Area Number |
23530938
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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 |
Clinical psychology
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| Research Institution | Fukuyama University |
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Principal Investigator |
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| Project Period (FY) |
2011 – 2013
|
| Project Status |
Completed (Fiscal Year 2013)
|
| Budget Amount *help |
¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2012: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2011: ¥520,000 (Direct Cost: ¥400,000、Indirect Cost: ¥120,000)
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| Keywords | レアシンドローム / プラダウイリー症候群 / 質的研究 / 障害受容 / FGI |
|---|
| Research Abstract |
This study was designed to investigate the nature of such burden that parents who have children with Prada-Willi syndrome are experiencing every day. Findings suggest that parents of children with rare diseases are not given sufficient information about disease conditions, and helping services are considered patchy in community settings. While families felt being isolated in their community, participating parents support group reflects perceived benefits, especially development and delivery of suggestions for effective treatments for children's problem behaviors. However, it was clear from the discussions that support from psychological professionals about rare conditions may obviously be scant and, therefore, there is an urgent need for establishing support system for rare diseases in community settings.
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