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Sökning: LAR1:lu > Högskolan i Jönköping > Fritt online

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1.
  • Adanko, Carina, 1970-, et al. (författare)
  • LED-belysning och brukaren
  • 2014
  • Rapport (övrigt vetenskapligt)abstract
    • Ljusforskning är om något diversifierad och omfattar teorier och metoder från skilda discipliner som teknik, medicin och samhällsvetenskap. Det finns också en förväntan att erhållna forskningsresultat skall kunna appliceras direkt i verkliga miljöer. I och med introduktionen av LED har många tidigare studier som behandlat glödlampor, lysrör och andra ljuskällor inaktualiserats. Ny kunskap - och ny forskning - krävs.En inventering av aktuell humanrelaterad LED-forskning genomfördes under 2013. Med utgångspunkt i detta material har föreliggande forskningsöversikt sammanställts. Totalt omfattar denna drygt 400 artiklar, som redovisas under följande rubriker: Den biologiska klockan; Flimmer och dimring av LED; Energibesparing: dagsljus och ljusstyrning; Färgåtergivning; Bländning och slutligen; Upplevda ljuskvaliteter.Såväl bakomliggande teoretiska resonemang som det aktuella kunskapsläget redovisas i de olika avsnitten. Efter varje avsnitt ges också referenser till relevanta forskningspublikationer. Samtliga publikationer har försetts med två eller flera svenska nyckelord, som anger publikationens innehåll. Publikationerna har sedan delars in i kategorier enligt avsnitten ovan. Efter varje avsnitt redovisas de publikationer på vilka texten baserar sig, med nyckelord. I ett slutavsnitt redovisas samtliga LED-publikationer i alfabetisk ordning efter författare och med nyckelord.
2.
  • Agren, Susanna, et al. (författare)
  • The Unsteady Mainstay of the Family: Now Adult Children's Retrospective View on Social Support in Relation to Their Parent's Heart Transplantation.
  • 2014
  • Ingår i: Nursing Research and Practice. - Hindawi Publishing Corporation. - 2090-1429. ; 2014
  • Tidskriftsartikel (refereegranskat)abstract
    • The needs for support among children with a seriously ill parent, who is waiting for heart transplantation, are unknown today. The aim was to describe now adult children's experiences of social support in relation to a parent's heart transplant during childhood. Nine females and four males were interviewed. The median age for the children was 18 at the transplantation and their parents had been ill before for 18 months (median) and on waiting list for 161 days (mean). Three categories emerged: health care professionals' approaches, family and friends' approaches, and society approaches. Our results show that there was lack of support for children of heart transplantation patients. Support in the shape of information was in most cases provided by the sick or healthy parent. It is of great clinical importance to develop psychosocial support programs for children with a seriously ill parent waiting for heart transplantation (before, during, and after surgery).
3.
  • Ahlström, Gerd, et al. (författare)
  • A comprehensive rehabilitation programme tailored to the needs of adults with muscular dystrophy
  • 2006
  • Ingår i: Clinical Rehabilitation. - 0269-2155. ; 20:2, s. 132-141
  • Tidskriftsartikel (refereegranskat)abstract
    • OBJECTIVE: To assess if activities of daily living (ADL), coping and quality of life could be improved in adults with muscular dystrophy through a comprehensive rehabilitation programme. DESIGN: Quasi-experimental, controlled clinical study comparing patients with similar age and disease aspects. SETTING: Two different counties in Sweden, being either study or control setting. SUBJECTS: The study group comprised 37 adults (21 women, 16 men; mean age 50 years), while the control group comprised 39 people (25 women, 14 men; mean age 46 years). INTERVENTIONS: Four rehabilitation sessions tailored to different medical, physical and psychosocial needs of the patients, comprising a total of 10 days over a period of 18 months. MAIN MEASURES: ADL, the Mental Adjustment to Cancer Scale measuring coping strategies, the Sickness Impact Profile measuring health-related quality of life, the Hospital Anxiety and Depression Scale, and the Psychosocial Well-being Questionnaire. RESULTS: No significant differences were found between groups with regard to the outcome measures. There was increased dependence on others in ADL after 18 months in both groups, but it was more pronounced in the control group. Furthermore, a clear trend was observed in the data with regard to coping patterns, the control group using more coping strategies such as 'Helplessness/hopelessness' (P= 0.057), 'Anxious preoccupation' (P = 0.085) and 'Fatalistic' (P= 0.073) when being compared to the study group. CONCLUSIONS: No apparent effects on ADL were found from the rehabilitation programme, although there was a tendency of reduction of maladaptive coping patterns in the study group. This initial study may provide the rationale and basis for a randomized controlled trial.
4.
  • Ahlström, Gerd, et al. (författare)
  • Assessment of coping with muscular dystrophy a methodological evaluation.
  • 1994
  • Ingår i: Journal of Advanced Nursing. - 0309-2402. ; 20:2, s. 314-323
  • Tidskriftsartikel (refereegranskat)abstract
    • There is no published research on coping with muscular dystrophy among adults. In the present study, two questionnaires, the Reaction to the Diagnosis of Cancer Questionnaire (RDCQ) and the Mental Adjustment to Cancer scale (MAC), were modified in order to measure coping with muscular dystrophy (MD). A total of 60 people (16-64 years) with diagnosed MD answered the questionnaires in two interviews including semi-structured questions. The replies to these questions were analysed by two independent judges on the basis of the RDCQ and MAC categories for coping. The purpose was twofold: to investigate if cancer-coping categories could be used for the classification of interview answers concerning coping with MD, and to gain knowledge about specific coping with MD. Analysis indicated that 82% of replies to semi-structured questions concerned with emotion/appraisal-focused coping with MD can be described by means of RDCQ and MAC categories. Eight new categories were developed to classify the remaining 18%: Anticipation, Creation of new life values, Minimization, Establishment of control over everyday life, Secretiveness, Fear, Social comparison and Coping with heredity. In addition, 997 replies were classified to represent problem-focused coping. The judges reached good agreement with respect to the proportions of replies in the respective coping categories. However, kappa (kappa) values were within the range of fair to good agreement.
5.
  • Ahlström, Gerd, et al. (författare)
  • Coping with illness-related problems and quality of life in adult individuals with muscular dystrophy.
  • 1996
  • Ingår i: Journal of Psychosomatic Research. - 0022-3999. ; 41:4, s. 365-376
  • Tidskriftsartikel (refereegranskat)abstract
    • Illness-related problems and coping were examined in 60 individuals with muscular dystrophy (MD) identified in a population survey of the county of Orebro, Sweden. In addition, the extent to which coping is related to quality of life (QoL) was investigated as was the impact of impairment and disability on the relation between coping and QoL. Emotion/appraisal-focused coping was utilized by respondents more than twice as often as problem-focused coping. High QoL was significantly correlated to "Stoic acceptance" and "Tried alternative treatment." Low QoL was associated with "Helpless/hopeless," "Anxious preoccupation," "Minimization," "Social comparison," "Establishment of control over everyday life," "Performs the task with the aid of an appliance" and "Accepts help or leaves it to others." When measures of impairment and disability were included in the analysis, the impact of these measures explained the association between coping and physical QoL by 16% to 43%.
6.
7.
  • Ahlström, Gerd, et al. (författare)
  • Disability and quality of life in individuals with muscular dystrophy.
  • 1996
  • Ingår i: Scandinavian Journal of Rehabilitation Medicine. - 0036-5505. ; 28:3, s. 147-157
  • Tidskriftsartikel (refereegranskat)abstract
    • In the county of Orebro, Sweden, 32 individuals with myotonic disorders and 25 with other types of muscular dystrophy were examined. Disability was assessed with functional tests and standardized observations of muscle function (mainly based on those proposed by Dr. Brooke), a new self-administered questionnaire regarding the Activities of Daily Living (ADL) and the ADL staircase (based on Katz ADL index). The results of the different tests of disability were highly correlated. The Sickness Impact Profile and the Kaasa test were used for assessing the quality of life, and no significant differences were found between the groups of muscular dystrophy. In an explanatory factor analysis three main factors of disability were found. The factors "walk and move" and "finger function" were fair to good associated with the quality of life. This study offers an approach for research on the consequences of muscular dystrophy using established as well as new methods.
8.
  • Ahlström, Gerd, et al. (författare)
  • Disability and quality of life in individuals with postpolio syndrome.
  • 2000
  • Ingår i: Disability and Rehabilitation. - 0963-8288. ; 22:9, s. 416-422
  • Tidskriftsartikel (refereegranskat)abstract
    • PURPOSE: The purpose of the study is to investigate disability and quality of life in individuals with the characteristic symptoms of postpolio syndrome. METHOD: Disability is assessed by means of the self-report activities of daily living instrument, and quality of life by means of Kaasa's questionnaire and the quality of life profile. RESULTS: The 39 subjects have on average lived with polio sequelae for 52 years. Their main difficulties are with moving, lifting and carrying. This means restricted mobility, sedentary activities and a need to prioritize. Half of them feel that polio has lessened their possibilities in life, and a quarter have still not accepted the limitations polio has involved. Nevertheless the majority report a high level of psychosocial well-being, and almost a quarter say that living with polio has meant personal development and strength. We found a significant correlation between on the one hand disability with regard to ambulation, arm strength and finger strength on the self-report ADL, and on the other hand the number of negative problems on the quality of life profile (0.33-0.45). CONCLUSION: The latter instrument needs further testing before its validity can be determined with certainty.
9.
  • Ahlström, Gerd, et al. (författare)
  • Encounters in close care relations from the perspective of personal assistants working with persons with severe disability.
  • 2010
  • Ingår i: Health & Social Care in the Community. - Wiley-Blackwell. - 0966-0410. ; 18:2, s. 180-188
  • Tidskriftsartikel (refereegranskat)abstract
    • Abstract In Sweden adults with major and sustainable disabilities can be granted publicly financed support in the form of personal assistance after assessment and decision-making in accordance with government rules. The purpose of the present study was to explore more deeply the encounters in close care relations between personal assistants and disabled persons of working age, as well as the prerequisites for and obstacles to the success of such encounters, this from the perspective of the personal assistants. Thirty-two personal assistants (22- to 55-year old) who worked for 32 persons with serious neurological diseases living at home were interviewed. The transcribed unstructured interviews were qualitatively analysed using latent content analysis. The analyses resulted in five main themes: Perceptive awareness, Entering into the other's role, Mutuality, Handling the relationship and Personal difficulties facing the assistant. These themes illustrated that a prerequisite for the encounter's being meaningful is that the assistant should be able to observe and understand the unique needs of the disabled person. The assistant must furthermore be able to put herself/himself into the other person's position. It is also important that the personal chemistry between the assistant and the disabled person should be good. Being able to share feelings and interests with the functionally impaired person provides the assistant with positive emotional confirmation of a good relationship. A distressing dilemma the assistant faces is that of distinguishing between the working relationship and the personal friendship. In this borderline area are found experiences, feelings and events that the assistant may view as negative or even unacceptable. This study contributes to the understanding of the complexity underlying the daily community care of disabled persons with an extensive need for care and assistance.
10.
  • Ahlström, Gerd, et al. (författare)
  • Epidemiology of neuromuscular diseases, including the postpolio sequelae, in a Swedish county.
  • 1993
  • Ingår i: Neuroepidemiology. - 0251-5350. ; 12:5, s. 262-269
  • Tidskriftsartikel (refereegranskat)abstract
    • The epidemiology of neuromuscular diseases was studied in the county of Orebro, Sweden (study population 270,000). Several different sources of data were utilized, compared and validated. On the prevalence of day (January 1, 1988) 474 patients were identified. The rate per 100,000 population was 92 for the postpolio sequelae (PPS) and 84 for the other neuromuscular diseases (motor neuron disease 9, hereditary neuropathies 9, myoneural disorders 16, myotonic disorders 19, muscular dystrophies 20 and myositis 11). Of the patients with the PPS, 80% reported late-onset symptoms. On the basis of an expanded survey including all medical records in one health care district, the prevalence of the PPS was estimated to be 186/100,000 population.
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