| Project/Area Number |
11307057
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Clinical nursing
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| Research Institution | St.Luke's Collage of Nursing |
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Principal Investigator |
KOMATSU Hiroko St.Luke's Collage of Nursing, Department of Nursing, Professor, 看護学部, 教授 (60158300)
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| Co-Investigator(Kenkyū-buntansha) |
HAYASHI Naoko St.Luke's Collage of Nursing, Department of Nursing, Lecturer, 看護学部, 講師 (30327978)
TONOSAKI Akiko St.Luke's Collage of Nursing, Department of Nursing, Lecturer, 看護学部, 講師 (20317621)
IBA Noriko St.Luke's Collage of Nursing, Department of Nursing, Lecturer, 看護学部, 講師 (00258980)
IIOKA Yukiko St.Luke's Collage of Nursing, Department of Nursing, Assistant, 看護学部, 助手 (40275318)
NAKAYAMA Yukiko St.Luke's Collage of Nursing, Department of Nursing, Assistant, 看護学部, 助手 (30338579)
橋爪 可織 聖路加看護大学, 看護学部, 助手 (20338578)
片桐 和子 聖路加看護大学, 看護学部, 助手 (80317627)
酒井 禎子 聖路加看護大学, 看護学部, 助手 (60307121)
高見沢 恵美子 聖路加看護大学, 看護学部, 助教授 (00286907)
南川 雅子 聖路加看護大学, 看護学部, 講師 (10255961)
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| Project Period (FY) |
1999 – 2002
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| Project Status |
Completed (Fiscal Year 2002)
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| Budget Amount *help |
¥28,340,000 (Direct Cost: ¥23,300,000、Indirect Cost: ¥5,040,000)
Fiscal Year 2002: ¥7,800,000 (Direct Cost: ¥6,000,000、Indirect Cost: ¥1,800,000)
Fiscal Year 2001: ¥14,040,000 (Direct Cost: ¥10,800,000、Indirect Cost: ¥3,240,000)
Fiscal Year 2000: ¥2,500,000 (Direct Cost: ¥2,500,000)
Fiscal Year 1999: ¥4,000,000 (Direct Cost: ¥4,000,000)
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| Keywords | cancer day care / beast cancer / post operative chemotherapy / outpatient setting / self-learning / support group / quasi-experimental research / がんデイケアモデル / がん患者 / がん医療システム / がんとの共生 / がんケアモデル |
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| Research Abstract |
The purpose of this research was to develop and evaluate a Cancer Day Care, Model (CDCM) as a new care system which helps patients living with cancer. In this final year of the research, clinical trials were conducted for further refinement and practical application of the model. The following outcomes were obtained. (1)After continual refinement, the CDCM was developed into a practical care program that included self learning materials (e.g. booklets, a log book, and video tapes), and a patients' support group program. (2)The program was examined for its relevance and appropriateness by a panel of oncology nurses, and members of a group of breast cancer patients, and modified. (3)As the preparation of the program operation, we collaborated with the outpatient sector of the research partner hospital for the program would be applied safely and efficiently, and held an educational workshop for nurses involved with the operation of the program. (4)The quasi experimental design research was conducted to test the program effects. To control exogenous variables, subjects were limited to those breast cancer patients receiving postoperative chemotherapy using epirubicin hydrochloride and cyclophosphamide in outpatient setting. To avoid contamination of data from both samples, data were collected first from the control group. Then, the program was provided to the experimental group by the nurses, who attended the educational workshop. As an immediate effect of the program, depression score was significantly reduced for the experimental group compared to the control group. For future research, we recommend further development and application of this CDCM that will more fully accommodate the background and preference of a wider group of cancer patients.
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