Hostname: page-component-848d4c4894-pjpqr Total loading time: 0 Render date: 2024-06-27T20:42:24.607Z Has data issue: false hasContentIssue false
  • English
  • Français

Services for Schizophrenic Patients and Their Families: What They Say They Need

Published online by Cambridge University Press:  16 June 2009

Amanda M. Reid ,
C. Mandy Lang  and
Tara O'Neill
Amanda M. Reid
Affiliation:
Harrogate District Hospital
C. Mandy Lang
Affiliation:
High Royds Hospital, West Yorkshire
Tara O'Neill
Affiliation:
High Royds Hospital, West Yorkshire
Get access Rights & Permissions [Opens in a new window]

Extract

The effects of education and stress reduction groups for the relatives of schizophrenic patients and their perception of services available to them is presented. 76% of relatives refused invitation to groups because they were overburdened. Those attending the groups said that they found them beneficial but measurable improvements were slight. Relatives' perception of the shortfalls of the services and the difficulties faced differed from that of patients. As the majority of patients turn to their relatives for help and support, rather than approaching hospital services directly, relatives were better able to identify service shortfalls. Patients' perceived needs included employment and increased income, which are not amenable to direct hospital intervention. Relatives were able to express needs that could be addressed by services. Both patients and relatives were able to identify the main difficulties faced, though there was a difference in emphasis.

Type
Clinical Section
Information
Behavioural and Cognitive Psychotherapy , Volume 21 , Issue 2 , April 1993 , pp. 107 - 113
Copyright
Copyright © British Association for Behavioural and Cognitive Psychotherapies 1993

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Birchwood, M., Smith, J., MacMillan, F., Hogg, B., Prasad, R., Harvey, C. and Bering, S. (1989). Predicting relapse in schizophrenia: the development and implementation of an early signs monitoring system using patients and families as observers, a preliminary investigation. Psychological Medicine 19, 649–656.CrossRefGoogle ScholarPubMed
Cochrane, R. (1980). A comparison of the symptom rating test and the Langner 22 item scale for use in epidemiological surveys. Psychological Medicine 10, 115–175.Google Scholar
Goldman, H. (1982). Mental illness and family burden: a public health perspective. Hospital and Community Psychiatry 33, 555–560.Google Scholar
Holden, D. and Lewine, R. (1982). How families evaluate mental health professionals, resources and effects of illness. Schizophrenia Bulletin 8, 626–633.Google Scholar
Kellner, R. and Sheffield, B. (1973). A self rating scale of distress. Psychological Medicine 3, 88–100.CrossRefGoogle ScholarPubMed
Pasamanick, B., Scarpitti, F. and Dinitz, S. (1967). Schizophrenics in the Community. New York: Appleton-Century-Crofts.Google Scholar
Smith, J. and Birchwood, M. (1985). Understanding Schizophrenia. Birmingham: Health Promotion Unit, West Birmingham Health Authority.Google Scholar
Smith, J. and Birchwood, M. (1987). Specific and non-specific intervention with families living with a schizophrenic relative. British Journal of Psychiatry 150, 645–652.CrossRefGoogle ScholarPubMed
Tarrier, N. (1991). Behavioural psychotherapy and schizophrenia: past, the present and the future. Behavioural Psychotherapy 19, 121–130.CrossRefGoogle Scholar
Tarrier, N. and Barrowclough, C. (1986). Providing information to relatives about schizophrenia: some comments. British Journal of Psychiatry 149, 458–463.CrossRefGoogle ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.