Client-centred rehabilitation: client perspectives

被引:266
作者
Cott, CA
机构
[1] Univ Toronto, Fac Med, Dept Phys Therapy, Toronto, ON M5G 1V7, Canada
[2] Univ Toronto, Grad Dept Rehabil Sci, Toronto, ON M5G 1V7, Canada
[3] Univ Hlth Network, Toronto Western Res Inst, Arthrit Community Res & Evaluat Unit, Toronto, ON, Canada
[4] Univ Toronto, Dept Publ Hlth Sci, Toronto, ON, Canada
关键词
D O I
10.1080/09638280400000237
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Purpose: The purpose of this research is to understand the important components of client-centred rehabilitation from the perspective of adult clients with long-term physical disabilities. Method: Focus groups were conducted with adult clients who had completed at least one course of rehabilitation in the publicly-funded rehabilitation system in Ontario. Data were analysed using an iterative inductive approach. Results: The major theme underlying all of the participants' comments was the need for better transitions between rehabilitation programs and the community. Participants felt ill-prepared for community living and the emotional challenges of living with a long-term condition and, once discharged from rehabilitation, felt isolated and had difficulty finding out about and accessing community services. Conclusions: The findings demonstrate that client-centred rehabilitation encompasses much more than goal-setting and decision-making between individual clients and professionals. It refers to a philosophy or approach to the delivery of rehabilitation services that reflects the needs of individuals and groups of clients. This entails a shift from an acute-illness, curative model to one that acknowledges the long-term nature of the career of chronic illness or disability. Definitions of evidence that is deemed credible need to be broadened beyond expert, 'scientific' evidence to include multiple dimensions of evidence including the expertise of the client.
引用
收藏
页码:1411 / 1422
页数:12
相关论文
共 63 条
[1]  
Albrecht G.L., 1992, The disability business: Rehabilitation in America
[2]  
[Anonymous], 1988, Living the Chronic Illness: The Experiences of Patients and Their Families
[3]  
[Anonymous], SYMBOLIC INTERACTION
[4]  
[Anonymous], CLIN REHABIL
[5]  
Barney G., 1967, Awareness of Dying, DOI DOI 10.4324/9780203793206
[6]  
Blumer H., 1969, Symbolic Interactionism: Perspective and Method
[7]   The role of the nurse in Patient-Focused Care: Models of competence and implications for education and training [J].
Burchell, H ;
Jenner, EA .
INTERNATIONAL JOURNAL OF NURSING STUDIES, 1996, 33 (01) :67-75
[8]   THE SOCIOLOGY OF CHRONIC ILLNESS - A REVIEW OF RESEARCH AND PROSPECTS [J].
BURY, M .
SOCIOLOGY OF HEALTH & ILLNESS, 1991, 13 (04) :451-468
[9]  
Bury M, 1982, Sociol Health Illn, V4, P167, DOI 10.1111/1467-9566.ep11339939
[10]  
Cardol M, 2002, DISABIL REHABIL, V24, P970, DOI 10.1080/09638280210151996