Syftet med studien var att undersöka hur manliga elitfotbollspelare (1) upplever stress under sin rehabilitering samt (2) vilka typer av strategier de använder sig av för att minska den upplevda stressen under sin rehabilitering. Elitfotbollspelarna (N=11) med en medelålder på 22 år besvarade en semistrukturerad intervjuguide gällande stress och coping under rehabilitering. Intervjuerna analyserades genom tematisk innehållsanalys. Resultatet visade att elitfotbollspelare upplever störst press och stress från sig själva och att det sociala nätverket är en viktig del för att handskas med upplevd stress. Resultatet visade även att positiv inställning är en viktig komponent för att få ett bra rehabiliteringsutfall. Resultatet från studien diskuterades i relation till relevant litteratur samt fyra utvalda teorier som tar upp de centrala begreppen i studien. / The purpose of this study was to examine how male elite soccer players (1) experience stress during their rehabilitation, and (2) what types of coping strategies they use to reduce the perceived stress during their rehabilitation. Elite soccer players (N = 11) with a mean age of 22 years responded to a constructed interview guide about current stress and coping during rehabilitationperiod. The interviews were analyzed by qualitative content analysis. The results showed that elite soccer players are experiencing the greatest pressure from themselves and to the social network is an important part to deal with the resulting pressure. The results also showed that positive attitudes are an important part leading to adaptive rehabilitation outcome. Results of the study were discussed in relation to relevant literature, and four selected theories that address the key concepts in the study

Syftet med studien är att belysa sjuksköterskors bedömningssituationer inom prehospital vård. Metod: I studien medverkar fyra män och fyra kvinnor med olika lång arbetslivserfarenhet inom prehospital vård. Alla arbetar i en region i mellan Sverige. Datainsamlingen genomfördes med hjälp av intervjuer. Intervjuerna analyserades med hjälp av kvalitativ innehålls analys. Resultat: Resultatet visar att bedöma sker utifrån tecken och symtom (vad sjuksköterskan ser, vad sjuksköterskan lyssnar till, vad erfarenheten säger, vad beslutstödet anger) och genom att skapa en god relation (förklara och informera, lugn skapar trygghet, delaktighet och samförstånd). Sammanfattning: Sjuksköterskan som är arbetsverksam inom ambulanssjukvården har så ofta som det är möjligt ett öppet sinne för att kunna göra rätt bedömning och beslut. Sjuksköterskan söker stöd från riktlinjer, och ibland även hos läkare. Men mest av allt söker de stöd från sin arbetslivserfarenhet. / Aim: The aim of this study was to enlighten nurses assessment situations in prehospital care.Method: Four men and four women participated in the study, all with a various length of experience from prehospital emergency care. All the interviewed participants are working in a region in the middle of Sweden. Interview data was analyzed with content analysis. Result: The results show that the assessments are based on signs and symptoms (what the nurse sees, what the nurse listens to, what experience tells, what decision support sets) and by creating a good relationship (explain and inform, calm creates confidence, participation and consensus) Summary: The nurse in the prehospital field performs assessments independently and uses an open mind to make correct assessments and decisions. They use their lived experiences to evaluate and to improve their ability to perform assessments. The nurse seeks support from guidelines, sometimes even physicians but most importantly they seek support from their lived experiences. They also try to improve the assessment capability of patients as often as possible.

ABSTRACT MEDIA, POLITICS AND SLANTED NEWS COVERAGE DURING THE ELECTION PERIODS &ndash / CASE STUDY OF NEWS ON AKP &Ccedil / AgLAYAN, Eda M.S. in Media and Cultural Studies Supervisor : Prof. Dr. RaSit KAYA May, 2010, 107 pages This thesis aims to study the attitude of media towards AKP (Adalet ve Kalkinma Partisi - Justice and Development Party) during the 2002 and 2007 general legislative elections in Turkey. Three national newspapers were selected in the scope of analysis: H&uuml / rriyet, Sabah an Yeni Safak in two months period before 2002 General Elections and 2007 General Elections (September, 1- October, 31 2002, June, 1 &ndash / July, 21 2007). Media are assumed to have a defining role on the formation of opinions due to the fact that the events of the external world to our immediate experiences is continuously interpreted and disseminated through them. Under these considerations, it is frequently claimed that world of politics is one of the most effected institutions. So, during the election periods campaigns are designed and carried out to direct opinions by means of media. Main question of the thesis is whether national daily newspapers were favorable to AKP, both before 2002 general elections when it was elected as first political party and before 2007 general elections when it was the ruling party. AKP news coverage of the selected newspapers in the defined periods were examined through qualitative content analysis. Selected newspapers&rsquo / news slant are revealed by way of reading AKP news critically to determine their dominant tone, gauging how much space they occupied in the newspapers and considering attitudes of the newspapers towards other political parties. Keywords: Media, Liberal Media Theory, News Slant, Qualitative Content Analysis

<p>The general aim of this thesis was to study the transition process from dependency towards anatomy and psychological empowerment among teenagers with type 1 diabetes. Thirty-two teenagers (18 female/14 male) aged 13-17 took part in conversational interviews. The interviews followed a semi-structured question guide. Data comprised 31 tape recorded interviews (one informant did not want to be tape recorded). The research design was based on a phenomenological and life world perspective including two different analysis methods.</p><p>The transition towards autonomy among teenagers with type 1 diabetes was elucidated in a phenomenological approach (paper I). Through the teenagers’ narratives about their daily life experiences with type 1 diabetes there emerged the over-riding theme “Hovering between individual actions and support of others”. This theme illustrates the main problem related to diabetes management - duality in dependence and independence. The themes “growth through individual self-reliance” and “growth through confirmation of others” seem to facilitate the transition process from dependency towards autonomy. Experiences of the Empowerment Education Programme (EEP) were studied by a qualitative content analysis (paper II). From the teenagers’ descriptions the over-riding theme was formulated as “Sense of community”, and this covered the categories of social fellow feeling, collaborative learning, and community of interests. A synthesis of the findings illustrates that individual self-reliance, confirmation of others, and sense of community are closely related to individual inner resources, trust in others, and the feeling of belonging, which are all suggested as specific goals of empowerment and fulfilment of psychological empowerment. A model was created to explain the relation between psychological empowerment and growth through individual self-reliance, confirmation of others, and sense of community. Professional nursing care might start from the unique situation and context the individual experiences and exists in. Social meetings with like-minded youth were highly appreciated among the teenagers. The teenagers showed their willingness to transform themselves towards becoming more independent in self-management, and the teenage years may be the right period to empower and coach the teenagers towards autonomy and prepare them for adulthood living with type 1 diabetes.</p>

No description available.

Background Inner strength has been described as an important phenomenon in association with disease management, health, and ageing. To increase the knowledge of the phenomenon of inner strength, a meta-theoretical analysis was performed which resulted in a model of Inner Strength where inner strength comprises four interrelated and interacting dimensions; connectedness, creativity, flexibility, and firmness. The model was used in this thesis as a theoretical framework. Aim The overall purpose of this thesis was to develop and validate an inner strength scale, describe inner strength among an older population, and elucidate its significance for experience of health, despite disease and adversities. Methods The studies had quantitative approaches with cross-sectional designs (I-III) and a qualitative approach with narrative interviews (IV). Studies I-IV was part of the GErontological Regional DAtabase (GERDA) Botnia project. In study I, the participants (n = 391, 19-90 years old) were mostly from northern Sweden. In studies II and III, the participants (n = 6119, 65, 70, 75 and 80 years old) were from Sweden and Finland, and in study IV the participants (n = 12, 67-82 years old) were from Västerbotten County. Data was analysed using principal component analysis and confirmatory factor analysis (CFA), various statistics, structural equation modelling, and qualitative content analysis. Results In study I, the Inner Strength Scale (ISS) was developed and psychometrically tested. An initial 63-item ISS was reduced to a final 20-item ISS. A four-factor solution based on the four dimensions of inner strength was supported, explaining 51% of the variance, and the CFA showed satisfactory goodness-of-fit. In study II, ISS scores in relation to age, gender and culture showed the highest mean ISS score among the 65-year-olds, with a decrease in mean score for every subsequent age (70, 75, and 80 years). Women had slightly higher mean ISS scores than men, and there were minor differences between the regions in Sweden and Finland. In study III, a hypothesis was proposed and subsequently supported in the results where inner strength was found to partially mediate in the relationship between disease and self-rated health. The bias-corrected bootstrap, estimating the mediating indirect effect was significant and the test of goodness-of-fit was satisfactory. In study IV, from the narratives of inner strength it was found that inner strength comprised feelings of being connected and finding life worth living. Having faith in oneself and one’s possibilities and facing and taking an active part in the situation were also expressed. Finally, coming back and finding ways to go forward in life were found to be essential aspects of inner strength. Conclusions The newly developed ISS is a reliable and valid instrument that captures a broad perspective of inner strength. Basic data about inner strength in a large population of old people in Sweden and Finland is provided, showing the highest mean ISS score among the 65-year-olds. Inner strength among old people is a resource for experience of health, despite disease and adversities. This thesis contributes to increase knowledge of the phenomenon of inner strength and provide evidence for the importance of inner strength for old people’s wellbeing. Increased knowledge of the four dimensions of inner strength; connectedness, creativity, flexibility and firmness, is proposed to serve as an aid for health care professionals in their efforts to identify where the need of support is greatest and to find interventions that promotes and strengthen inner strength. / Bakgrund Inre styrka har beskrivits som ett viktigt fenomen associerat till att hantera sjukdom, till hälsa och åldrande. För att öka kunskapen om fenomenet inre styrka genomfördes en metateoretisk analys som resulterade i en Inre Styrka modell där inre styrka omfattar fyra samverkande dimensioner; samhörighet, kreativitet, flexibilitet och fasthet. Modellen har använts i denna avhandling som ett teoretiskt ramverk. Syfte Det övergripande syftet med denna avhandling var att utveckla och testa en skala som mäter inre styrka, beskriva inre styrka i en population av äldre, och att belysa dess betydelse för upplevelsen av hälsa, trots sjukdom 0ch motgångar. Metod Studierna som genomfördes hade kvantitativ ansats med tvärsnittsdesign (I-III) och kvalitativ ansats med narrativa intervjuer (IV).  Alla studier var en del av GErontologiska Regionala DAtabas (GERDA) Botnia projektet. Deltagarna i studie I (n= 391, 19-90 år) var mestadels från norra delarna av Sverige. I studierna II och III var deltagarna (n=6119, 65, 70, 75 och 80 år) från Sverige och Finland. I studie IV var deltagarna (n=12, 67-82 år) från Västerbotten. Data analyserades med hjälp av principalkomponentanalys och konfirmatorisk faktor analys (CFA), varierande statistik, strukturell ekvationsmodellering, och kvalitativ innehållsanalys. Resultat I studie I utvecklades och testades Inre Styrka Skalan (ISS). En inledande 63 frågors ISS reducerades till en slutlig 20 frågors ISS. Baserad på de fyra dimensionerna av inre styrka bekräftades en fyrafaktors lösning med 51 % förklaringsgrad och CFA visade ett tillfredställande goodness-of-fit. I studie II beskrevs inre styrka i relation till ålder, kön och kultur. Det högsta totala ISS medelvärdet skattades bland 65-åringarna med lägre medelvärden för varje efterföljande ålder (70, 75 och 80 år). Kvinnor skattade ett något högre totalt ISS medelvärde än män och det var inte några större skillnader mellan regionerna i Sverige och Finland. I studie III bekräftades den hypotes som lagts fram, att inre styrka kan mediera i relationen mellan sjukdom och upplevelsen av hälsa. Bias-corrected bootstrap visade en signifikant indirekt effekt i relationen mellan sjukdom och upplevelsen av hälsa, medierad av inre styrka, och test av modellens goodness-of-fit var tillfredsställande. I studie IV, utifrån berättelserna om inre styrka visade det sig att inre styrka omfattar känslor av samhörighet och att finna livet värt att leva. Att ha tillit till sig själv och sina möjligheter, och att kunna möta och ta aktiv del i situationen beskrevs också. Slutligen, att komma igen och hitta vägar att gå vidare i livet var viktiga aspekter av inre styrka.  Slutsatser Den nyutvecklade Inre Styrka Skalan är ett reliabelt och valitt instrument som fångar ett brett perspektiv av inre styrka. Basdata om inre styrka i en stor population äldre i Sverige och Finland har presenterats, och visar det högsta ISS medelvärdet bland 65-åringarna. Inre styrka bland äldre är en resurs för upplevelsen av hälsa, trots sjukdom och motgångar. Denna avhandling bidrar till att öka kunskapen om fenomenet inre styrka och ger evidens för att inre styrka har en viktig betydelse för äldres välbefinnande. Ökad kunskap om de fyra dimensionerna av inre styrka; samhörighet, kreativitet, flexibilitet, och fasthet, föreslås kunna vara en hjälp för vårdpersonal i deras arbete att identifiera var behovet av stöd är störst och att sätta in insatser som främjar och stärker inre styrka. / GErontologiska Regionala DAtabas (GERDA) Botnia projektet

Introduction: Patient participation is important for improving outcomes and respecting selfdetermination and legal aspects in care. Heart failure is a chronic condition that puts high demands on self-care and patient participation. Patients often need advanced care due to deterioration of their heart failure symptoms, and one option is to provide care as home-care. There is limited knowledge of how patients with heart failure and their partners view participation in home-care. Aim: The overall aim of this thesis was to describe different perspectives of participation in structured heart failure home-care among patients with heart failure and their partners. Methods: All patients in this thesis received structured heart failure home-care, according to a model aiming to facilitate care, where safety, participation, and gaining knowledge about the illness and treatment, are in focus. Study I had a prospective pre-post longitudinal design including 100 patients with heart failure receiving home-care. Data was collected by selfadministered questionnaires. Study II had a descriptive design. Nineteen patients receiving home-care were interviewed, and data was analysed using qualitative content analysis. Study III had a descriptive and explorative design. Data was collected by video-recorded observations of 19 home visits and analysed by qualitative content analysis. Study IV had a parallel convergent mixed-method design including 15 partners of patients receiving structured home-care. Data was collected by interviews and self-administered questionnaires. Datasets were first analysed separately and then together. Results: Better self-care behaviour was significantly associated with all measured aspects of participation. Participation by received information increased significantly during the 12-month follow-up (I). Patients’ descriptions of participation included communication between patients and health care professionals, access to care, active involvement in care, a trustful relation with health care professionals, and options for decision-making(II). Observed care encounters revealed that participation was made possible by; (i) interaction, including exchange of care-related information, care-related reasoning, and collaboration, (ii) an enabling approach, including the patient expresses own wishes and shows an active interest, and the nurse is committed and invites to a dialogue (III). Partners scored fairly positive for their participation in care and they performed different levels of caregiving tasks. Descriptions of participation included; adapting to the caring needs and illness trajectory, mastering caregiving demands, interacting with care providers, and gaining knowledge to comprehend the health situation. The mixed-method results showed both convergent results and expanded knowledge (IV). Conclusions: Structured heart failure home-care facilitated participation both for patients and their partners. Patient participation with regard to received information improved significantly after receiving home-care. Aspects of patient participation were consistently associated with better self-care behaviour. Patients’ and partners’ descriptions revealed many aspects of participation, and observed home visits revealed how interaction and an enabling approach underpinned participation.

The overall aim of this thesis was to explore and describe women’s recovery after a first myocardial infarction (MI) from an organisational, a relational and an individual perspective. In this thesis a longitudinal, explorative and descriptive design combining both quantitative (papers I-II) and qualitative (papers III-IV) methods has been used. Data was collected from healthcare professionals at 18 acute hospitals (paper I), which on two occasions answered a questionnaire dealing with cardiac rehabilitation efforts. From these 18 hospitals, 240 women who had suffereda first MI (paper II) were consecutively chosen to answer a questionnaire on three occasions on the subject of social support and social network. Descriptive and inferential statistics were used to analyse data over time. Paper III and IV had an exploratory and descriptive design based on an inductive, qualitative content analysis approach. Interviews were conducted with 20 cardiac rehabilitation nurses (CRN) (paper III) and with 26 women suffering a first MI (paper IV). The results showed that patients with MI, and their next of kin, were offered a well-functioning cardiac rehabilitation on both measurement occasions. None of the hospitals offered a CRP that was specifically designed for women (paper I). The women perceived that the extent of general support, support from relatives, and professional support changed positively over time (paper II). The CRNs experienced that women’s recovery was influenced by their ability to cope with the stresses of life, if they wanted to be involved in their own personal care and how they related to themselves, and their opportunities to receive support (paper III). Women experienced that ability to approach the new perspective of life depended on how they embraced the three dimensions; behaviour, i.e. women’s acting and engaging in various activities, social i.e. how women receive and give support in their social environment, and psychological i.e. their way of thinking, reflect and appreciate life (paper IV). In conclusion, the four studies show that women’s recovery after a first MI is depending on factors emerging from an organisational, a relational and an individual perspective. Using knowledge from these three perspectives the possibility of a holistic approach to women’s recovery process to health will increase and the risk of a reductionist thinking will decrease.

The objective of this research was to study how two newspapers in Sweden, Aftonbladet and Expressen are creating an image of the Stockholm suburb Rinkeby. The method used to do the study was qualitative content analysis. Ten articles were chosen, five off either newspaper and were found on the internet homepages of the newspapers on 15 November of 2013 and 27 January of 2014. Several theories were used in the study. Agenda setting theory, a media theory that explains the power of media, Figuration theory developed by Norbert Elias that deals with power struggles between different groups in society. Labeling theory explains how society, by labeling someone a “criminal” may accept it as an own identity and become one. Mats Franzén theory of power and how it can be understood thru discourse, context and resources. While studying the subject I realized that for long time the suburbs of Sweden have been portrayed in a negative context, especially “famous” suburbs like Rinkeby. The suburbs’ are constructed by the media as very dangerous places, with young people (often males) running wild and engaging in destructive behavior.

The Swedish health care system does not offer care on equal terms for all its end-users. Discrimination toward patients can take the form substandard communication toward women or foreign born patients. Discrimination is also embedded in the organizational context. Health care is under pressure to increase efficiency and quality of care at the same time. There is a risk that demands for equality will be pushed aside. This thesis aims to contribute to our understanding of how discrimination is expressed in interpersonal- and organizational communication within health care, and highlight educational implications for health care practices. This thesis is comprised of three empirical studies and one conceptual study. In the first study, critical discourse analysis (CDA) is used to categorize gender patterns in communication between health care workers and patients, and finds that both patients and health care workers reproduced the gender order. Open questions created a setting less prone to be limited by gender stereotypes. In the second study, CDA is used and complemented with Linell’s dialogic perspective in order to explore whether patients who were native speakers of Swedish were constructed differently than those who were not, in patient-physician consultations. Findings indicated that the non-native speakers actually were model, participative patients according to patient-centered care. Notwithstanding this they were met by argumentation, whereas the more amenable native patients were met by accommodating responses. In the third study, qualitative content analysis is used to analyze how health care workers talked about patients in their absence. The results revealed that communication about patients who were perceived as not acting according to socially accepted gender norms contained negative and disparaging statements. The final study focused on Clinical Microsystems, a New Public Management-based model for multi-professional collaboration and improvement of health care delivery. Drawing on theories of New Public Management, gender, and organizational control, this study argues that the construction of innovative and flexible health care workers risks reproducing the gender order. The thesis concludes that gender and ethnic stereotypes are reproduced in health care communication, and that an efficiency-inspired organizational and institutional discourse may be an impediment to equal care. This calls for focus on learning about communication for prospective and existing health care workers in a multicultural health care context.