<p>The aim with the literature study was to describe how persons with dementia and health care workers in the geriatric care experiences soft massage and to describe the derived effects for persons with dementia. Scientific articles were sampled from the databases: Medline (Pub Med), Cinahl and Psyc INFO. The main results of the study are presented in three parts: how persons with dementia experiences soft massage, health care workers experiences of giving soft massage and the health care workers descriptions on derived effects on persons with dementia. The results showed that persons with dementia experienced a positive reaction to soft massage and the health care workers did no longer feel helpless in their care service towards persons with dementia. The studies showed that soft massage decreased agitation, wandering, pain and sleeplessness. Not all persons with dementia was receptive to soft massage, therefore an ethical awareness was required by the health care workers.</p>

Thesis (Ph. D.)--University of Texas at Austin, 2006. / Vita. Includes bibliographical references.

The aim with the literature study was to describe how persons with dementia and health care workers in the geriatric care experiences soft massage and to describe the derived effects for persons with dementia. Scientific articles were sampled from the databases: Medline (Pub Med), Cinahl and Psyc INFO. The main results of the study are presented in three parts: how persons with dementia experiences soft massage, health care workers experiences of giving soft massage and the health care workers descriptions on derived effects on persons with dementia. The results showed that persons with dementia experienced a positive reaction to soft massage and the health care workers did no longer feel helpless in their care service towards persons with dementia. The studies showed that soft massage decreased agitation, wandering, pain and sleeplessness. Not all persons with dementia was receptive to soft massage, therefore an ethical awareness was required by the health care workers.

Thesis (Ph. D.)--University of Oregon, 2003. / Typescript. Includes vita and abstract. Includes bibliographical references (leaves 150-160). Also available for download via the World Wide Web; free to University of Oregon users.

Not available / text

No description available.

Diagnosis with a serious chronic illness is a powerful lived experience that touches all aspects of the individual’s life and which necessitates great adaptation across the lifespan. Ambiguity is a lived dimension of illness that is often expressed in illness stories, capturing the new state between health and illness which has also been described as a ‘liminal’ or in-between state of being (Little, Jordens, Paul, Montgomery & Philipson, 1998). Health care providers hold socially prescribed roles in which they are expected to be professionally competent and immune to personal illness. The lived experiences of health care providers who have been diagnosed with serious chronic illness were explored in this study to better attempt to describe the phenomenon. Six health care providers from various professional backgrounds participated in the research. A semi-structured interview guided the conversation between the researcher and the participant. The participants were encouraged to tell the story of what has happened to them and to reflect on the impact to their lives and practice. Participants were also asked to reflect on their perceived level of support and preparedness via their professional training, and to share any recommendations they might have for others going through this experience. The data gathered were found to be rich in both depth and detail. The data were analyzed using van Manen’s interpretive phenomenological method. Significant statements created formulated meanings or categories, which became organized around eight themes. The themes formed several clusters. The theme clusters were then developed into a recognizable pattern of sub-themes which helped to further 7 describe the essence of the experience of health care providers living with serious, chronic illness. The findings of the research were found to be consistent with the literature that describes the lived experience of seriously ill health care providers as liminal in essence. Based on the research findings recommendations for social work practice, administration and policy, educational training reform and future research were outlined.

Syftet med föreliggande studie var att redogöra för hälso- och sjukvårdspersonalens följsamhet till hygienföreskrifter avseende handhygien och de faktorer som påverkar detta. Metod: Artiklar söktes via CINAHL, Pubmed och Scopus. Sökord som användes i olika kombinationer var: hand hygiene, adherence, hygiene guidelines, health care workers, compliance, hand disinfection, infection control, nursing, nurse och hand cleansing. Tretton vetenskapliga artiklar erhölls. Vidare gjordes en manuell sökning ifrån inkluderade artiklars referenslistor och genererade två artiklar som ingick i resultatet. Resultat: Resultatet visade att hälso- och sjukvårdspersonalens följsamhet till hygienföreskrifter avseende handhygien var låg. Vidare framkom av resultatet att det fanns sju kategorier av faktorer som påverkade följsamheten till hygienföreskrifterna. Dessa var: utbildning och kunskap, arbetsbelastning och tidsbrist, tillgänglighet, hudproblem och handskar. Slutsats: Följsamheten till hygienföreskrifter avseende handhygien är låg. Kontinuerlig utbildning i kombination med ökad tillgänglighet och minskad arbetsbelastning är de viktigaste förutsättningarna för att öka följsamheten till hygienföreskrifter gällande handhygien.

Diagnosis with a serious chronic illness is a powerful lived experience that touches all aspects of the individual’s life and which necessitates great adaptation across the lifespan. Ambiguity is a lived dimension of illness that is often expressed in illness stories, capturing the new state between health and illness which has also been described as a ‘liminal’ or in-between state of being (Little, Jordens, Paul, Montgomery & Philipson, 1998). Health care providers hold socially prescribed roles in which they are expected to be professionally competent and immune to personal illness. The lived experiences of health care providers who have been diagnosed with serious chronic illness were explored in this study to better attempt to describe the phenomenon. Six health care providers from various professional backgrounds participated in the research. A semi-structured interview guided the conversation between the researcher and the participant. The participants were encouraged to tell the story of what has happened to them and to reflect on the impact to their lives and practice. Participants were also asked to reflect on their perceived level of support and preparedness via their professional training, and to share any recommendations they might have for others going through this experience. The data gathered were found to be rich in both depth and detail. The data were analyzed using van Manen’s interpretive phenomenological method. Significant statements created formulated meanings or categories, which became organized around eight themes. The themes formed several clusters. The theme clusters were then developed into a recognizable pattern of sub-themes which helped to further 7 describe the essence of the experience of health care providers living with serious, chronic illness. The findings of the research were found to be consistent with the literature that describes the lived experience of seriously ill health care providers as liminal in essence. Based on the research findings recommendations for social work practice, administration and policy, educational training reform and future research were outlined.

Thesis (MHlthSc(OccTh))--University of South Australia, 1999