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Sökning: hsv:(SAMHÄLLSVETENSKAP) hsv:(Sociologi) > Högskolan Dalarna > Marie Cederschiöld högskola

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1.
  • Knezevic, Zlatana, fil.dr. 1984-, et al. (författare)
  • De/gendering Violence and Racialising Blame in Swedish Child Welfare – What Has Childhood Got to Do with It?
  • 2023
  • Ingår i: Journal of Gender-Based Violence. - : Bristol University Press/Policy Press. - 2398-6808 .- 2398-6816. ; 50
  • Tidskriftsartikel (refereegranskat)abstract
    • This article is a critical interrogation of how gender and power figure in Swedish child welfare policy and the discourses on violence in intimate relationships vis-à-vis children exposed to violence. Drawing on feminist violence research, critical childhood studies, and intersectional perspectives, we identify a differentiation with racialised undertones in the understanding of violence as a social problem when related to children’s exposure. While predominately gender-neutral discourses of social heredity and epidemiology run through the material for the seemingly ‘universal’ child, forms of violence ascribed to the presumed cultural Others link to gender, structural power, and sexuality. The article concludes that gendered articulations of violence are restricted yet pivotal if children’s exposure is to be linked to issues of inequality and power. However, when gendering interlinks with racialisation, problematic differentiations of violence, childhoods, and children are produced.
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3.
  • Eriksson, Maria, 1969-, et al. (författare)
  • Taking children exposed to intimate partner violence seriously? : developments in BBIC from 2006 to 2015
  • 2016
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
    • To improve child protection investigations the framework for assessment ”BBIC – Barns Behov I Centrum” [Children’s needs in the centre] was introduced in Sweden just after the new millennium, with the first full training resource published in 2006. There is a lack of research in Sweden about child protection work in cases of intimate partner violence generally and as regards BBIC specifically. However, a number of different sources indicate that there is a need for improvement of the BBIC system when it comes to this group of children at risk. For example, the national inspections of the local authorities’ work with abused women and children exposed to intimate partner violence carried out so far point to serious problems in child protection practice. Since BBIC was introduced the system has been amended and revised several times. A major revision was carried out in 2015. An important question is what these revisions may mean for the handling of cases of intimate partner violence. The aim of the paper is to map and assess how the issue of children’s exposure to violence has been addressed in the different versions of BBIC between 2006 and 2015. Surveying training resources and other documents from the last decade, we outline how there has been a gradual and partial inclusion of the issue of children’s exposure to violence over time, and discuss to what extent these amendments constitute a shift in perspective and emphasis major enough to be likely to impact positively on practice.
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4.
  • Stier, Jonas, et al. (författare)
  • Leadership culture and the position of girls and young women within elite gymnastics
  • 2015
  • Ingår i: Differences, Inequalities and Sociological Imagination. - 9788073302726 ; , s. 243-243
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
    • Mainstream discourse on sport and young people brings positive aspects, such as enjoyment, development and health promotion to the fore. Sport is also presumed to be secure. Drawing on a study of leadership culture within Swedish elite gymnastics, the paper examines how coaches and gymnasts approach issues such as food and diet, weight and weight control, injuries and pain, sport relationships (coach-gymnast, coach-gymnast-parents, coach-sport association, etcetera), knowledge and competence, as well as the relationship between leadership culture and policy documents such as the National guidelines for elite gymnastics and the UN convention on the rights of the child. The analysis brings the gendering practices of the coaches – often an adult man - to the fore and indicates that girls and young women are subjected to more control, verbal abuse, and stricter demands on both obedience and diet than boys and young men. Boys and young men seem to be treated more democratically and receive more positive feedback and social support. These results are discussed in relation to the intersection of age and gender inequality, as well as constructions of both gender and the child, for example, how the treatment of girls and young women is associated with a well-established notion that female gymnasts need a child-like body to be able to perform at the elite level. Furthermore, prevailing conceptions of the optimal body of a successful gymnast is discussed, particularly in the light of the pubertal development of girl's' and boys' bodies.
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5.
  • Jegermalm, Magnus, 1962-, et al. (författare)
  • Links between informal caregiving and volunteering in Sweden : a 17-year perspective
  • 2013
  • Ingår i: European Journal of Social Work. - : Informa UK Limited. - 1369-1457 .- 1468-2664. ; 16:2, s. 205-219
  • Tidskriftsartikel (refereegranskat)abstract
    • This article analyses informal caregiving and volunteering in organizations over 17 years in Sweden, with a focus on links between these two forms of unpaid activities. The discussion is based on results from a national survey that was repeated four times in the period 1992–2009. Links were found between the different types of activities. In all four studies a substantial group of the population was involved both in informal caregiving and volunteering. This group of ‘active citizens’ are commonly also engaged in informal social networks. This ‘double active’ group had increased over time and they provide a substantial amount of hours of involvement. Patterns outlined in this article demonstrate that unpaid activities represent a multifaceted phenomenon, and that the boundaries between informal caregiving and volunteering as forms of engagement may be more fluid than has previously been acknowledged. The results challenge the literature in which informal caregiving is viewed as a major obstacle to volunteering. At the same time, however, informal caregiving in general was found to be increasing. There might be reasons to be cautious about the possible risk that too much pressure on citizens for informal caregiving might jeopardize the type of double involvement that is outlined in this article.
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6.
  • Eriksson, Maria, et al. (författare)
  • Barn som offer och aktörer
  • 2008
  • Ingår i: Sociologisk forskning. - : Sveriges sociologförbund. - 0038-0342 .- 2002-066X. ; 45:2, s. 81-86
  • Tidskriftsartikel (refereegranskat)
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7.
  • Ewertzon, Mats, 1956- (författare)
  • Familjemedlem till person med psykossjukdom : bemötande och utanförskap i psykiatrisk vård
  • 2012
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • This thesis focused on the situation of family members of persons with psychotic illness, particular on their experience of the approach of the healthcare professionals and of their feelings of alienation regarding the professional care of their family member. A further aim was to explore how siblings who have participated in a support group for siblings experienced their situation.A questionnaire was developed that enabled the aims of this thesis to be investigated (I). Seventy family members from various parts of Sweden participated, and data were collected via the questionnaire developed in study I (II-III). Thirteen siblings who previously had participated in a support group participated in follow-up focus groups interviews (IV).The questionnaire developed was shown to be reliable and valid in these studies (I). In many cases, the participants had experienced an approach from professionals that indicated that they did not experience openness, confirmation and cooperation, and that they felt powerless and socially isolated in relation to the care. There was also found to be a certain degree of association between how the participants experienced the approach and whether they felt alienation (II). The majority of the participants considered openness, confirmation, and cooperation to be important aspects of professional’s approach. The result also identified a low level of agreement between the participants’ experience and what they considered to be significant in the professional’s approach (III). The findings revealed the complexity of being a sibling of an individual with psychotic illness. Participating in a support group for siblings can be of importance in gaining knowledge and minimizing feelings of being alone (IV).Although the psychiatric care services in Sweden have been aware of the importance of cooperating with family members, the results indicated that there is a need for further research in this area. 
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8.
  • Ayoub, Maria, 1990-, et al. (författare)
  • The Family Talk Intervention in Pediatric Oncology : Potential Effects Reported by Parents
  • 2024
  • Ingår i: Children. - : MDPI. - 2227-9067. ; 11:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Childhood cancer impacts the family system and has psychosocial consequences for all family members. For the parents, the ill child, and the siblings to be able to adjust to this challenging situation, the whole family needs access to psychosocial support. However, only a few such family interventions in pediatric oncology have been evaluated. The aim of this study was to explore the potential effects of a family-centered intervention, the Family Talk Intervention (FTI), in pediatric oncology from the parents' perspectives. Methods: A concurrent mixed methods design was used for this study. Data were derived from a pilot study of 26 families recruited from one pediatric oncology center in Sweden. This study focused on questionnaire and interview data from 52 parents. Results: After participation in FTI, the parents felt more satisfied with the conversations within the family about the illness. FTI also contributed to strengthened family togetherness, including more open communication and improved family relations, as described by the parents. Parents further expressed that they felt more empowered in their parenting role following FTI. Conclusions: The findings regarding FTI's ability to improve family communication and family relations, thus strengthening family togetherness in families with childhood cancer, are promising. This provides motivation for a large-scale study of FTIs in pediatric oncology.
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9.
  • Jegermalm, Magnus, et al. (författare)
  • Carers in Sweden : The public support they receive, and the support they desire
  • 2013
  • Ingår i: Journal of Care Services Management. - : Maney Publishing. - 1750-1679 .- 1750-1687. ; 7:1, s. 17-25
  • Tidskriftsartikel (refereegranskat)abstract
    • This article describes and analyses public support for Swedish unpaid carers, now mandated by law, and also the support that they desire, using surveys conducted in 2008, 2009, and later. Few carers helping someone in a different household – the large majority of the carers – received any support aimed directly at them, such as access to support groups, training, relief service, or financial support. Yet, most carers did not desire any support for themselves. They mostly wanted public services for the cared-for person, all of which may also indirectly support carers. Intra-household carers – about a tenth of all carers – have vastly larger care commitments than other carers. Some of them desire support for themselves, usually relief services of financial support. Three out of 10 of these carers used any public support, despite the new (2009) legislation that only a minority of carers know about. There is a wide gap between policies and their implementation, but also some reluctance among carers to use public support for themselves. The relationship between carers and the state is unclear in Sweden and this reflects on the aims and the forms of support. Stereotypes about ‘typical’ carers may have impeded adequate forms of support.
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10.
  • Jegermalm, Magnus (författare)
  • Carers in the Welfare State : On Informal Care and Support for Carers in Sweden
  • 2005
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • The general aim of this dissertation is to describe and analyse patterns of informal care and support for carers in Sweden. One specific aim is to study patterns of informal care from a broad population perspective in terms of types of care and types of carer. A typology of four different care categories based on what carers do revealed that women were much more likely than men to be involved at the ‘heavy end’ of caring, i.e. providing personal care in combination with a variety of other caring tasks. Men were more likely than women to provide some kind of practical help (Study I).Another aim is to investigate which support services are received by which types of informal caregiver. Relatively few informal caregivers in any care category were found to be receiving any kind of support from municipalities or voluntary organizations, for example training or financial assistance (Study II).The same study also examines which kinds of help care recipients receive in addition to that provided by informal carers. It appears that people in receipt of personal care from an informal caregiver quite often also receive help from the public care system, in this case mostly municipal services. However, the majority of those receiving personal, informal care did not receive any help from the public care system or from voluntary organizations or for-profit agencies (Study II).The empirical material in studies I and II comprises survey data from telephone interviews with a random sample of residents in the County of Stockholm aged between 18 and 84.In a number of countries there is a growing interest among social scientists and social policymakers in examining the types of support services that might be needed by people who provide informal care for older people and others. A further aim of the present dissertation is therefore to describe and analyse the carer support that is provided by municipalities and voluntary organizations in Sweden. The dissertation examines whether this support is aimed directly or indirectly at caregivers and discusses whether the Swedish government’s special financial investment in help for carers actually led to any changes in the support provided by municipalities and voluntary organisations. The main types of carer support offered by the municipalities were payment for care-giving, relief services and day care. The chief forms of carer support provided by the voluntary organizations were support groups, training groups, and a number of services aimed primarily at the elderly care recipients (Study III).Patterns of change in municipal carer support could be discerned fairly soon. The Swedish government’s special allocation to municipalities and voluntary organisations appears to have led to an increase in the number of municipalities providing direct support for carers, such as training, information material and professional caregiver consultants. On the other hand, only minor changes could be discerned in the pattern of carer support services provided by the voluntary organizations. This demonstrates stability and the relatively low impact that policy initiatives seem to have on voluntary organizations as providers (Study IV).In studies III and IV the empirical material consists of survey data from mail questionnaires sent to municipalities and voluntary organizations in the County of Stockholm.In the fields of social planning and social work there appears to be a need to clarify the aims of support services for informal carers. Should the support be direct or indirect? Should it be used to supplement or substitute caregivers? In this process of reappraisal it will be important to take the needs of both caregivers and care recipients into account when developing existing and new forms of support. How informal caregivers and care recipients interact with the care system as a whole is undeniably a fertile field for further research.
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