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Nursing Research and Practice
Volume 2012 (2012), Article ID 568242, 14 pages
Research Article

Psychosocial Well-Being in Persons with Aphasia Participating in a Nursing Intervention after Stroke

1Department of Nursing Science, Faculty of Medicine, Institute of Health and Society, University of Oslo, P.O. Box 1130 Blindern, 0318 Oslo, Norway
2Department of Nursing and Mental Health, Faculty of Public Health, Hedmark University College, P.O. Box 400, 2418 Elverum, Norway
3Institute of Public Health, University of Århus, Nordre Ringgade 1, 8000 Århus C, Denmark
4Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, P.O. Box 1171 Blindern, 0318 Oslo, Norway
5Department of Geriatric Medicine, Oslo University Hospital, P.O. Box 4956 Nydalen, 0424 Oslo, Norway

Received 19 March 2012; Accepted 10 May 2012

Academic Editor: Kim Usher

Copyright © 2012 Berit Arnesveen Bronken et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The psychosocial adjustment process after stroke is complicated and protracted. The language is the most important tool for making sense of experiences and for human interplay, making persons with aphasia especially prone to psychosocial problems. Persons with aphasia are systematically excluded from research projects due to methodological challenges. This study explored how seven persons with aphasia experienced participating in a complex nursing intervention aimed at supporting the psychosocial adjustment process and promoting psychosocial well-being. The intervention was organized as an individual, dialogue-based collaboration process based upon ideas from “Guided self-determination.” The content addressed psychosocial issues as mood, social relationships, meaningful activities, identity, and body changes. Principles from “Supported conversation for adults with aphasia” were used to facilitate the conversations. The data were obtained by participant observation during the intervention, qualitative interviews 2 weeks, 6 months, and 12 months after the intervention and by standardized clinical instruments prior to the intervention and at 2 weeks and 12 months after the intervention. Assistance in narrating about themselves and their experiences with illness, psychological support and motivation to move on during the difficult adjustment process, and exchange of knowledge and information were experienced as beneficial and important by the participants in this study.