The purpose of the current study was to examine delinquent pre-adolecents. It was hypothesized that both predictor variable [exposure to community violence (number of events; preception of events) and stressful life events (number of events)] would impact delinquent behavior (violent thoughts, violent behaviors, and promiscuity).

This study explores stress levels among a population of Master of Social Work (MSW) students enrolled at California State University, San Bernardino (CSUSB). It is hypothesized that student stress is related to curriculum, finances, gender, and social roles.

Introduktion: Traumatisk hjärnskada är en av det ledande orsakerna till mortalitet och morbiditet globalt. Traumatisk hjärnskada graderas som mild, måttlig eller svår skada. Prognosen kan variera beroende på allvarlighetsgraden, långvarig medvetslöshet samt storleken på primär och sekundär skada. De förlorade eller nedsatta funktioner som hjärnskadan medfört kan i olika grad påverka individers livssituation. Syfte: Syftet med denna studie var att beskriva hur individer med en traumatisk hjärnskada upplever sin livssituation tiden efter den akuta fasen av skadan. Metod: En kvalitativ systematisk litteraturstudie med beskrivande design. Studiens resultat baserades på 10 vetenskapliga originalartiklar från databaserna PubMed och CINAHL. Resultat: Fyra huvudkategorier identifierades: komplikationer, ett annat liv, mötet med hälso- och sjukvården samt vardagen med traumatisk hjärnskada. De mest framträdande komplikationerna var fysiska, kognitiva och psykosociala svårigheter. En förändrad självbild och att acceptera skadan gav upphov till känslan av ett annat liv efter skadan. Information, kommunikation och stöd var viktiga delar i mötet med hälso- och sjukvården. Vardagen med traumatisk hjärnskada omfattade närståendes betydelse, arbetsliv och återhämtning vilket var viktiga delar för en fungerande vardag. Slutsats: Individer som drabbats av traumatisk hjärnskada upplever i olika grad att livet förändras efter skadan. Hur komplikationer inverkar på livet, känslan av ett annat liv, mötet med hälso- och sjukvården samt vardagen med traumatisk hjärnskada var dominerande upplevelser som alla påverkade och kunde förändra individens livssituation. Upplevelserna av en förändrad livssituation kan bidra till känslan av att inte fylla sin funktion i livet vilket kan resultera i en minskad känsla av sammanhang. För att tillmötesgå dessa individer och optimera förutsättningarna krävs god information, kommunikation, förståelse och planering från hälso- och sjukvården och samhället.  Nyckelord: traumatisk hjärnskada, vuxna, livsavgörande händelser, känsla av sammanhang, kvalitativ systematisk litteraturstudie / Introduction: Traumatic brain injury is a worldwide leading cause of death and disability. Traumatic brain injuries can be graded as mild, moderate and severe. The prognosis can vary depending on severity, length of unconsciousness and the size of the primary and/or secondary trauma. The reduced or lost functions that the brain injury brings can to various extents influence individuals’ life situation. Purpose: The purpose of this study was to describe how individuals with a traumatic brain injury experience their life situation following the acute phase of the injury.  Method: Qualitative systematic literature study with a descriptive design. The result of the study is based on 10 scientific original articles from the databases PubMed and CINAHL. Results: Four main categories were identified: Complications, Another life, Encounter with healthcare and Daily life with traumatic brain injury. The most prominent complications were physical, cognitive and psychosocial difficulties. A changed self-perception and to accept the injury contributed to the sense of another life after the injury. Information, communication and support were crucial factors in the encounter with healthcare. Daily life with traumatic brain injury included the importance of relatives, working life and recovery which were important factors for a functional daily life. Conclusion: Individuals with traumatic brain injury experience life changes in varying degrees after the injury. Important aspects of the individuals’ life situation included: impact of complications, a feeling of a different life, encounters with healthcare and perceptions of daily life. The experiences of life changes may contribute to a feeling of not being able to fulfill life's duties. That may result in a lower sense of coherence. Adjustment and improvement of the conditions for these individuals require adequate information, communication, understanding and planning from healthcare and society.  Keywords: traumatic brain injury, adults, life change events, sense of coherence, qualitative systematic literature study Introduction: Traumatic brain injury is a worldwide leading cause of death and disability. Traumatic brain injuries can be graded as mild, moderate and severe. The prognosis can vary depending on severity, length of unconsciousness and the size of the primary and/or secondary trauma. The reduced or lost functions that the brain injury brings can to various extents influence individuals’ life situation. Purpose: The purpose of this study was to describe how individuals with a traumatic brain injury experience their life situation following the acute phase of the injury.  Method: Qualitative systematic literature study with a descriptive design. The result of the study is based on 10 scientific original articles from the databases PubMed and CINAHL. Results: Four main categories were identified: Complications, Another life, Encounter with healthcare and Daily life with traumatic brain injury. The most prominent complications were physical, cognitive and psychosocial difficulties. A changed self-perception and to accept the injury contributed to the sense of another life after the injury. Information, communication and support were crucial factors in the encounter with healthcare. Daily life with traumatic brain injury included the importance of relatives, working life and recovery which were important factors for a functional daily life. Conclusion: Individuals with traumatic brain injury experience life changes in varying degrees after the injury. Important aspects of the individuals’ life situation included: impact of complications, a feeling of a different life, encounters with healthcare and perceptions of daily life. The experiences of life changes may contribute to a feeling of not being able to fulfill life's duties. That may result in a lower sense of coherence. Adjustment and improvement of the conditions for these individuals require adequate information, communication, understanding and planning from healthcare and society.  Keywords: traumatic brain injury, adults, life change events, sense of coherence, qualitative systematic literature study

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Bakgrund: Diabetes typ 2 har utvecklats till en global folksjukdom och utgör cirka 90 % av all diabetes. Kända orsaker till att insjukna i T2D är ärftlighet, ålder och dåliga levnadsvanor. En stor del av behandlingen består av egenvård och patienten har eget ansvar över sin sjukdom. För att kunna utföra egenvård på rätt sätt krävs det att patienter har kunskap om hur kost, motion och andra faktorer påverkar deras blodsockernivåer. Utmaningar och svårigheter som patienter upplever vid utförande av egenvård kommer att styra deras behov av kunskap samt stöd och därför är det viktigt att som sjuksköterska ha en förståelse om detta.   Syfte: Denna studies syfte var att beskriva patienter med diabetes typ 2 upplevelser av sin egenvård.  Metod: Systematisk litteraturöversikt som utgick från 14 vetenskapliga studier med kvalitativ ansats. Den analysmetod som användes var innehållsanalys. Resultat: Tre kategorier och 7 subkategorier kunde synliggöras. De tre kategorierna var Upplevelser av inre faktorer som hindrar genomförandet av egenvård, Upplevelser av inre faktorer som främjar genomförandet av egenvård samt Upplevelser av yttre faktorer som påverkar genomförandet av egenvård.  Konklusion: För att kunna erbjuda personcentrerad vård måste sjuksköterskan ha en förståelse för de hinder som patienter upplever vid utförandet av egenvård. Resultatet i denna studie visade att många patienter saknade kunskap om kosthållning och motion vilket inverkade negativt på deras sjukdomshantering. Patienter upplevde även utmaningar i att hantera de känslor som var vanligt förekommande samt de utökade krav som sjukdomen bidrog till. Faktorer som främjade genomförandet av egenvård var motivation, självinsikt samt acceptans och patienter upplevde att omgivningen hade en stor påverkan på deras förmåga att göra livsstilsförändringar. I och med komplexiteten på sjukdomen är det viktigt att behandlingen utformas och anpassas efter varje patients individuella behov och önskemål. / Background: Type 2 diabetes has developed into a global public disease and may account for about 90 percent for all diagnosed cases of diabetes. Known causes of T2D disease are heredity, older age and unhealthy lifestyle behaviors. Self-management is an important part of diabetes treatment and the patients have a responsibility over their illness. To be able to manage self-care in the right way requires that patients have knowledge about how diet, exercise and other factors affect their blood sugar levels. The challenges and difficulties that patients experience while managing self-care will control their need for knowledge and support and that is why it is important for nurses to have an understanding of these issues. Aim: The aim of this study was to describe how patients with type 2 diabetes experience their self-management.  Method: Systematic literature review based on 14 scientific studies with a qualitative approach. The analysis method used was content analysis. Result: Three categories and seven subcategories were identified and presented in this study. The three categories were Experiences of internal factors that hinder the implementation of self-care, Experiences of internal factors that promote the implementation of self-care and Experiences of external factors that affect the implementation of self-care.   Conclusion: To be able to offer patient centered care nurses need an understanding of the obstacles that patients experience when practicing self-care. The result of this study showed that a lot of patients lacked knowledge about nutrition and physical exercise which had a negative effect on their self-management behaviors. Patients also experienced challenges in dealing with common emotions and the increase of requirements that came along with the disease. Supporting factors that promoted self-care were motivation, self-perception and acceptance and patients experienced that the social environment had a major impact on their ability to make lifestyle changes. As a result of the complexity of the disease it is important that treatment is designed and adapted to every patient’s individual needs and wishes.

by Kwong Lai-king. / Thesis (M.A.Ed.)--Chinese University of Hong Kong, 1991. / Bibliography: leaves 106-119. / ACKNOWLEDGEMENTS --- p.ii / LIST OP TABLES --- p.vi / LIST OF FIGURES --- p.vii / ABSTRACT --- p.viii / Chapter CHAPTER ONE： --- INTRODUCTION / Chapter 1. --- Background of the Problem: Adolescents in Hong Kong --- p.1 / Chapter 2. --- Purposes of the Study --- p.9 / Chapter 3. --- Significance of the Study --- p.10 / Chapter CHAPTER TWO： --- REVIEW OF RELATED LITERATURE / Chapter 1. --- Definition of Stress --- p.12 / Chapter 2. --- Life Events and Stress --- p.14 / Chapter 3. --- Adolescents and Stress --- p.23 / Chapter 4. --- Life Events and Stress Symptoms --- p.34 / Chapter 5. --- Type A/B Behaviour Pattern and Stress --- p.36 / Chapter 6. --- Adolescents' Coping Strategies When Facing Stressful Life Events --- p.39 / Chapter CHAPTER THREE： --- METHOD / Chapter 1. --- Framework of the Study --- p.46 / Chapter 2. --- Definition of Terms --- p.48 / Chapter 3. --- Null Hypotheses --- p.49 / Chapter 4. --- Sample --- p.49 / Chapter 5. --- Instruments --- p.50 / Chapter 6. --- Procedures --- p.57 / Chapter 7. --- Data Analysis --- p.59 / Chapter CHAPTER FOUR： --- RESULTS AND DISCUSSION / Chapter 1. --- Characteristics of the Sample in the Main Study --- p.62 / Chapter 2. --- Reliabilities of Instruments --- p.65 / Chapter 3. --- Major Life Events Happened to Form 6 students --- p.67 / Chapter 4. --- stress Symptoms Experienced by Form 6 students --- p.76 / Chapter 5. --- Type A/B Behaviour Pattern of Form 6 students --- p.80 / Chapter 6. --- Ways of Coping of Form 6 students --- p.83 / Chapter 7. --- "Relationship among Life Events, Stress, Type A/B Behaviour Pattern and Ways of Coping" --- p.87 / Chapter 8. --- Limitations of the Present Study --- p.94 / Chapter CHAPTER FIVE： --- SUMMARY AND RECOMMENDATION / Chapter 1. --- Summary of Findings --- p.95 / Chapter 2. --- Importance of Findings --- p.97 / Chapter 3. --- Recommendation --- p.103 / BIBLIOGRAPHY --- p.106 / APPENDICES --- p.120 / Chapter Appendix A: --- Life Events Checklist --- p.120 / Chapter Appendix B: --- Modified Life Events Checklist (Translated version) --- p.121 / Chapter Appendix C: --- Type A Questionnaire --- p.122 / Chapter Appendix D: --- General Health Questionnaire --- p.123 / Chapter Appendix E: --- Ways of Coping --- p.125 / Chapter Appendix F: --- Test Battery (Translated version) --- p.126

The results of this study revealed that despite the childhood sexual abuse event, the victims were able to change their views in a positive direction with regard to the benevolence of the world and people as they marched through life and presumably experienced positive events.

The family is a miniature society, where a child is afforded the opportunity to develop, form relationships and create his/her own identity. The child's development does not always take place without certain challenges. Different internal and external factors influence a child's development. Certain external factors, for instance a child with disabilities, can have a negative or positive influence on the child. The aim of this study is to determine the influence of the child with Cerebral Palsy on the social and emotional development of siblings. The research will be done using the idiographic method. The results show that the child with Cerebral Palsy does have an influence on the emotional and social development of siblings. / Educational Studies / M.Ed. (Inclusive Education)

As a result of the Zimbabwean socio-economic and political crisis many have joined the Diaspora leaving their children behind in the care of others. Qualitative research in the form of in-depth semi-structured interviews carried out with seventeen adolescent Zimbabwean Diaspora orphans evidenced a number of emerging themes that illuminate how these adolescents view their situation, such as symptomology of depression, feelings of abandonment and rejection, conflicting feelings, lack of social support, the importance of communication, role changes and additions, materialism, challenges presented by relationships with caregivers, and vulnerability to sexual abuse and molestation. Most of the themes do not appear to be country specific but are shared by adolescent Diaspora orphans world-wide. Defence and coping mechanisms employed by these adolescents to cope with parental absence were also identified. Recommendations aimed at optimising their integration in society and suggestions for further research in this field conclude this study. / Psychology / M.A. (Psychology)

published_or_final_version / Social Work / Master / Master of Social Work