Sökning: "professional caregivers"

Visar resultat 11 - 15 av 50 avhandlingar innehållade orden professional caregivers.

  1. 11. A moral endeavour in a demoralizing context: Psychiatric inpatient care from the perspective of professional caregivers

    Författare :Sebastian Gabrielsson; Stefan Sävenstedt; Malin Olsson; Rolf Adolfsson; Ulla Hällgren Graneheim; Luleå tekniska universitet; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Nursing; Inpatient care; Psychiatry; focus group; Qualitative methods; Concept development; Person-centred care; Content Analysis; Interviews; Medicine; Medicin; Nursing; Omvårdnad;

    Sammanfattning : Patients in psychiatric care experience a need for and expect to develop interpersonal relationships with professional caregivers and to be respected and listened to. Despite demands for care to be person-centred and recovery-oriented, patients experience that psychiatric inpatient care fails to meet their expectations. LÄS MER

  3. 12. Assessment in Evidence-Based Practice : Psychometric Properties, Clinical Utility and Professional Co-operation from Different Perspectives of the Home Observation for Measurement of the Environment in Sweden

    Författare :Johan Glad; Karin Sonnander; Ulla Jergeby; Carina Gustafsson; Laura Ferrer-Wreder; Uppsala universitet; []
    Nyckelord :SAMHÄLLSVETENSKAP; SOCIAL SCIENCES; HOME Inventory; Social work assessment; Assessment instruments; Clinical utility; Evidence-based practice; Psychometric properties; Professional co-operation; Medicinsk vetenskap; Medical Science;

    Sammanfattning : The overall aim of the present thesis was to explore and compare professional co-operation in child welfare investigations, explore the psychometric properties, and describe the clinical utility from different perspectives of a translated Swedish version of the standardized assessment instrument the Home Observation for Measurement of the Environment (the HOME Inventory). Social workers in Sweden, Denmark, Britain, Germany, and Texas (USA) co-operated with different professionals around a fictitious child welfare case. LÄS MER

  4. 13. Paradoxer i välfärden : När anhöriga blir lösningen på demensomsorgens utmaningar

    Författare :Emme-Li Vingare; Ulla Melin Emilsson; Lottie Giertz; Marjaana Seppänen; Linnéuniversitetet; []
    Nyckelord :SAMHÄLLSVETENSKAP; SOCIAL SCIENCES; family caregivers; dementia care; welfare paradoxes; familisation; systems; functions; anhöriga; demensomsorg; välfärdsparadoxer; familisering; system; funktioner; Socialt arbete; Social Work;

    Sammanfattning : This thesis addresses dementia care in Sweden and the function family caregivers are given. The aim of the thesis is to analyse critically the system of municipal eldercare and the function of family caregivers in this system, and in various types of organisations. LÄS MER

  5. 14. Vårdandets Tao : En fenomenologisk studie om vårdrelationer i Kina

    Författare :Judy Chow; karin Dahlberg; Jan Bärmark; Växjö universitet; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; care; caring; professional- relations; relationship; nurse-patient relationship; China; cross-cultural care study; Lifeworld; ethics; cargiver; patient.; vård; vårdande; vårdrelation; Kina; etik; fenomenologi; Tao; Vårdvetenskap; systematiska vårdvetenskap; Caring sciences; Vårdvetenskap; Vårdvetenskap; Caring Science;

    Sammanfattning : This thesis researches the phenomenon ‘caring relationship’. The empirical studies in this thesis were carried out in China with the aim to describe the caring relationship in China through the lifeworld experiences of professional caregivers and patients. The result of this study will later on relate to a study of Swedish caring relationships. LÄS MER

  7. 15. Consequences for family members of being informal caregivers to a person with advanced cancer

    Författare :Catarina Sjölander; Jönköping University; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES;

    Sammanfattning : Aim: The overall aim is to generate knowledge about consequences of informal caregiving for the family members of patients diagnosed with advanced cancer, over a one-year period, including the family members’ health, health-related quality of life, health care utilization, and associated costs. Furthermore, the family members’ management of their stressful daily life and the meanings of social support networks in the early stage will be explored in order to get deeper understanding. LÄS MER