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Träfflista för sökning "WFRF:(Svensson Tommy 1950 ) "

Sökning: WFRF:(Svensson Tommy 1950 )

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1.
  • Biong, Stian, et al. (författare)
  • Metaphors of a shifting sense of self in men recovering from substance abuse and suicidal behavior
  • 2008
  • Ingår i: Journal of Psychosocial Nursing and Mental Health Services. - : SLACK, Inc.. - 0279-3695 .- 1938-2413. ; 46:4, s. 35-41
  • Tidskriftsartikel (refereegranskat)abstract
    • The purpose of this descriptive study was to explore and interpret men's experience of sense of self within the context of recovery from substance abuse and suicidal behavior. A secondary analysis of data from a previous study of four young Norwegian men revealed how a shifting sense of self was constructed through the use of metaphors. The analysis identified three themes related to the participants' sense of self: The Meaning of Being Isolated, The Meaning of Being Close to the Point of No Return, and The Meaning of Still Being on the Edge. By acknowledging metaphorical expressions as a source of important knowledge, this study reflects on how mental health professionals can use metaphors in the recovery process. As part of the treatment alliance and therapeutic communication, we suggest that metaphors may aid the assessment of suicidal ideation, promote a sense of a more active self, and signal acceptance and recognition of subjectivity.
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2.
  • Björklund, Anita, et al. (författare)
  • A longitudinal study on the transformation of 15 occupational therapist students'paradigms into occupational therapists' paradigms
  • 2006
  • Ingår i: Australian Occupational Therapy Journal. - : Wiley. - 0045-0766 .- 1440-1630. ; 53:2, s. 87-97
  • Tidskriftsartikel (refereegranskat)abstract
    • Background and Aim: This study describes the transformation of 15 occupational therapist students'paradigms into occupational therapists'paradigms according to Törnebohm's theory of paradigms over a period of 6 years. This research particularly considers the paradigm components world view and field of action view in Törnbohm's sense. Method: Qualitative data were collected using essay questions on three occasions: First week and last semester at the Occupational Therapy Programme at the School of Health Sciences, Jönköping, Sweden, and after 3 years of occupational therapy practice. A content analysis of the collected materials was performed. Conclusion: The transformation of the informants'views could be characterised as comprising three different perspectives: A 'public'view in 1995, a 'theoretical' view in 1998 and an 'experiential/contextual' view in 2001. © 2006 The Authors Journal compilation © 2006 Australian Association of Occupational Therapists.
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  • Björklund, Anita, et al. (författare)
  • Holistic and biomedical concepts of health : A study of health notions among Swedish occupational therapists and a suggestion for developing an instrument for comparative studies
  • 2006
  • Ingår i: Scandinavian Journal of Occupational Therapy. - : Informa UK Limited. - 1103-8128 .- 1651-2014. ; 13:3, s. 141-150
  • Tidskriftsartikel (refereegranskat)abstract
    • The objectives of this study were to inquire into notions of health among a group of 439 Swedish occupational therapists and to test a model derived from a qualitative study by Björklund & Svensson with a representative sample of occupational therapists in Sweden. The data were collected through a questionnaire and were analyzed using descriptive statistics, cluster analysis, and confirmatory factor analysis. The means and ranking of the health notions showed that Swedish occupational therapists most frequently hold holistic notions of health, and to a lesser extent biostatistical ones. Most Swedish occupational therapists indicate that being clearly conscious of one's health notions is important both to themselves and to their profession. The test of the model provides a step towards developing an instrument for measuring notions of health that clearly distinguishes between holistic and biomedical ones and that could possibly be used for comparative studies.
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6.
  • Bülow, Per, et al. (författare)
  • Att vara sin sjukdom : Om psykiskt funktionshinder och åldrande
  • 2008. - 1
  • Ingår i: Att åldras med funktionshinder. - Lund : Studentlitteratur. ; , s. 165-193
  • Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
    • Vi har hittills haft begränsad kunskap om funktionshindrade människors liv över tid och om innebörden i att leva med funktionshinder under många år. Vad innebär det att åldras med funktionshinder? Hur gestaltar sig "äldreblivandet" om man redan har betydande funktionsnedsättningar sedan tidigare i livet och kanske tvingats lämna arbetslivet långt före gängse pensionsålder? Hur är det att, som en till åren kommen förälder, fortfarande vara den som hjälper sitt vuxna, funtionshindrade barn? Hur ser den formella och informella omsorgssituationen ut? Det är frågor som den här boken belyser och den fyller därmed ett viktigt kunskapsbehov. Boken utgår från ett livsloppsperspektiv. Den centrala frågan är sålunda hur livet idag gestaltar sig för funktionshindrade människor som vuxit upp och levt under vissa historiska villkor. Här ryms även ett anhörigperspektiv där denna fråga studeras på motsvarande sätt. Bokens sex kapitel diskuterar de här frågorna med olika tonvikt och med utgångspunkt från både fysiskt och psykiskt funktionshindrades förhållanden. Samtliga författare bedriver forskning med anknytning till bokens huvudfråga. Att åldras med funktionshinder riktar sig främst till högskolestuderande inom samhälls- och beteendevetenskap, socialt arbete, social omsorg och vård, liksom till yrkesverksamma inom fältet. Den kan också vara värdefull för en intresserad allmänhet.
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  • Fredriksen, Sven-Tore D., et al. (författare)
  • Body, strength and movement - Intensive care patients' experience of body
  • 2008
  • Ingår i: International Journal of Qualitative Studies on Health and Well-being. - : Informa UK Limited. - 1748-2623 .- 1748-2631. ; 3:2, s. 77-88
  • Tidskriftsartikel (refereegranskat)abstract
    • This study is about intensive care patients' experience of strength, body and movement during critical illness in an intensive care unit. The aim of the study is to inquire and understand the ways the body and its experience appear when the phenomena of strength and movement are altered. The data were collected through in-depth interviews with seven patients and analysed from a phenomenological-hermeneutical point of view. The findings showed a body that refuses to cooperate and is often marginally able to cope with the situation at all. It showed relational bonding between the patients and health personnel and/or significant others where the patients were overlooked and at the same time dependent on the same persons. They were waving between life and death through dimension of existence, which is contrasted to earlier experiences. They showed feeling responsible for the family through a role in to reduce their fears. At the same time, they are in a continuous struggle for life in which they balance between vague hope and a situation so challenging that the only thing left is grim humour. They showed progressing and expectations where the slightest changes in the situation in a positive direction create a hope in them.
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10.
  • Gustafsson Stolt, Ulrica, 1965-, et al. (författare)
  • Information and informed consent in a longitudinal screening involving children : a questionnaire survey
  • 2005
  • Ingår i: European Journal of Human Genetics. - : Springer Science and Business Media LLC. - 1018-4813 .- 1476-5438. ; 13, s. 376-383
  • Tidskriftsartikel (refereegranskat)abstract
    • This empirical study explores participants' perceptions of information and understanding of their children's and their own involvement in a longitudinal screening, the ABIS Study. ABIS (All Babies In Southeast Sweden) is a multicentre, longitudinal research screening for Type 1 diabetes and multifactorial diseases involving 17 005 children and their families. For this study, a random selection of mothers was made, using perinatal questionnaire serial numbers from the ABIS study. In total, 293 of these mothers completed an anonymous questionnaire (response rate 73.3%). Our findings from the questionnaire indicate a marked difference between the reported satisfaction with and understanding of the information provided on the one hand and the significant lack of knowledge of some of the aims and methods of the ABIS screening on the other, namely concerning high-risk identification of involved children, potential prevention and future questionnaires. Two questions evoked by our results are: (1) what information is required for participants in longitudinal studies involving children? and (2) how do we ensure and sustain understanding, and thus in a prolonging, informed consent in these studies? This study underlines the importance of an increased understanding of the ethical issues that longitudinal research on children raise and the need to discuss how information and informed consent strategies should be analysed and designed in longitudinal studies.
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