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No description available.

Bakgrund: Vårdnadsbelastning och stress är vanligt bland anhörigvårdare till personer med demens eller långvarig sjukdom. Minfulness-Based Stress Reduction (MBSR) är en tänkbar fysioterapeutisk intervention för denna grupp. Syfte: Att genomföra en systematisk litteraturstudie i syfte att kartlägga effekt, risk för snedvridning och tillförlitlighet med MBSR som behandlingsmetod för stress och vårdnadsbelastning för anhörigvårdgivare. Metod: En systematisk litteraturöversikt av randomiserade kontrollerade studier genomfördes i databaserna PubMed och PsychInfo. TestEx användes för att bedöma kvaliteten av de utvalda artiklar och tillförlitligheten granskades med granskningsmallen Bedömning av den sammanvägda tillförlitligheten i systematiska översikter. Resultat: Åtta artiklar inkluderades i denna studie och deltagarna var alla anhörigvårdgivare till vuxna personer med långvarig sjukdom. Sju undersökte vårdnadsbelastning och fem undersökte stress. Ingen signifikant skillnad observerades på vårdnadsbelastning. Stress minskades signifikant i tre av fem studier. Kvalitetsgranskning med TextEx resulterade i fyra artiklar med hög kvalitet och fyra med låg. Av de fyra med hög kvalitet gick två att sammanväga för tillförlighet, men dessa bedömdes ha mycket låg tillförlighet. Konklusion: Resultatet baseras på två studier som kunde sammanvägas med kontrollgruppen “ingen behandling”. Dessa visade mycket låg tillförlitlighet för att MBSR hade effekt på stress och vårdnadsbelastning. / Objective: Caregiver burden and stress are common challenges faced by family caregivers of individuals with dementia or chronic illness. Additionally, Mindfulness-Based Stress Reduction (MBSR) is a potential physiotherapeutic intervention for this group. Aim: To assess the effectiveness, risk of bias, and reliability of MBSR as a method of treatment for stress and caregiver burden among informal caregivers. Method: A systematic literature review of randomized controlled trials was conducted using the databases PubMed and PsychInfo. TestEx was used to assess the quality of the chosen studies, and reliability was evaluated using the template to assess the reliability of the results. Results: Eight articles were included in this study and the participants were informal caregivers to adults with chronic illness. Seven investigated caregiver burden, while five examined stress. No significant difference was observed in caregiver burden. However, stress was significantly reduced in three out of five studies. The quality assessment using TestEx resulted in four articles being classified as high quality, and four as low quality. Among the high-quality articles, two could be combined for reliability assessment, but they were deemed to have very low reliability. Conclusion: The results are based on two studies that could be combined with the control group “no treatment”. These studies showed very low reliability regarding MBSR as a treatment of stress and caregiver burden for informal caregivers.

Made available in DSpace on 2016-06-02T19:45:57Z (GMT). No. of bitstreams: 1 DissLZMA.pdf: 788184 bytes, checksum: 487fa9a5ccb31dc3ce033b97c8610d15 (MD5) Previous issue date: 2007-06-15 / Universidade Federal de Sao Carlos / Considering the highest increasing of the elderly population in our country and simultaneously the increasing of morbidity rate of chronic-degenerative disease, in general, there are people seeking to be in attendance, at day centre or hospital; these people are dependents on and when come back home, need familial caregivers. The caregivers are the fundamental importance to keep the patient in his community, to prevent and treat the problems caused by the stress factors among them must contribute to reduce or to postpone the hospitalization of caregivers. Besides, the improvement on quality of life could give the caregivers do better help to patients by influencing positively on the chronic disease course. So, this research try to undestand the reality of the caregivers lifes who s relatives are chronic illnesses pacientes. With this knowlege, implement and evaluate the effectiveness of an intervention proposal with caregivers. The objective of this intervention is to attenuate the happened stress conditions of the care activities. The research will use interview with caregivers at USE, at Federal University at S.Carlos; this interview will be taped and latter, a transcription to analyze the content of answers and to elaborate the intervention plan, in that case, a course. The course will consist of informative aspect about disease and daily life activities, as well as, formative aspect about self knowledge. A quality of life instrument named Caregiver Burden Scale will be given to caregivers. After the intervention (course) the Scale will be give once more to verify the date and to check the efficacy of intervention. / Intervenção: suporte para cuidadores de doentes crônicos através do ensino. Considerando-se o acelerado aumento da população idosa em nosso país e simultaneamente o aumento do índice de morbidade de doenças crônico-degenerativas em geral, temos observado cada vez mais o aumento do número de pessoas buscando atendimento, tanto em nível ambulatorial quanto hospitalar, estas pessoas são muitas vezes dependentes e quando retornam para suas casas precisam receber cuidados de algum membro da família, o cuidador. Sendo os cuidadores de fundamental importância para manter o paciente na comunidade, a prevenção e o tratamento dos problemas (produzidos pelo impacto de fatores estressantes) entre os cuidadores podem contribuir para se reduzir ou protelar a institucionalização. Além do mais, a melhora na qualidade de vida dos cuidadores possibilita-lhes prestar melhor assistência aos pacientes, influenciando positivamente o curso da doença crônica. Assim, esta pesquisa tem como objetivo identificar a realidade de cuidadores de pacientes portadores de doenças crônicas e, a partir deste reconhecimento, implementar e avaliar a eficácia de uma proposta de intervenção junto a cuidadores que objetiva atenuar as condições estressantes advindas das práticas de cuidado. Utilizará para tanto, entrevistas com cuidadores familiares, abordados em uma Unidade Saúde Escola (USE), estas entrevistas serão gravadas e posteriormente transcritas para análise do conteúdo e elaboração da intervenção, no caso um curso, onde serão abordados aspectos informativos sobre a patologia e as atividades desempenhadas no cotidiano, assim como, aspectos formativos como o autoconhecimento; também nesta primeira fase será aplicado um instrumento de qualidade de vida denominado Caregiver Burden Scale. Após a intervenção o instrumento será aplicado novamente para ser possível um confronto de dados e verificar a eficiência da intervenção.

No description available.

Caring for a family member who is ill can be a draining experience (Cooper et al., 2006; Daire, 2002; Zarit et al, 1980). Providing care for a family member that is living with HIV/AIDS is potentially even more stressful because of social meanings associated with HIV/AIDS infection (Stajduhar, 1998) and the contagious nature of the HIV virus (Powell-Cope & Brown, 1992). Research indicates that most caregivers are female (Bunting, 2001; Songwathana, 2000). In Africa women bear the brunt of the burden of providing care for family members who are living with HIV/AIDS (Mushonga, 2001; Olenja, 1999). This study examined coping factors and caregiver burden among female caregivers (N=116) of a family member living with HIV/AIDS in Kenya. Coping factors were derived from a principal components factor analysis of the fourteen scales on the Brief Cope (Carver, 1997). Caregiver burden was measured using the Zarit Caregiver Burden Inventory. Multiple regression analysis was used to investigate the relationships between caregiver burden and coping factors. Post–hoc multiple regression analyses further investigated the relationship between caregiver burden and caregiver demographic characteristics. The relationship between caregiver burden and care recipient characteristics was also investigated. The principle components factor analysis of the Brief Cope yielded five coping factors that were labeled: Social support, Hope, Acceptance, Planning, and Disposition. The regression analysis that was conducted to investigate the relationships between these five coping factors and caregiver burden indicated a significant inverse relationship between Hope and caregiver burden. The post-hoc analyses investigating the relationship between various caregiver and care recipient characteristics indicated a significant relationship between the caregiver's age and caregiver burden, and education level and caregiver burden. An increase in age correlated with a decrease in caregiver burden. An increase in education level correlated with reduced caregiver burden. Implications of the findings for research and practice are discussed.

Personality characteristics of spousal and adult children and active potential caregivers of persons with Alzheimer's Disease were studied in order to better predict caregiver burden and aspects of well-being. Contrary to prediction, no differences were found between spouse and adult children active caregivers on measures of well-being. Additionally, adult children potential caregivers indicated feeling less control over their lives than spouse potential caregivers. When social desirability was controlled, active caregivers reported greater fluctuations in affect than did potential caregivers. As predicted, personality characteristics of individuals were found to have the biggest role in determining which individuals experience stress or burden.

Stroke är den tredje vanligaste dödsorsaken i Sverige och risken för att insjukna ökar med stigande ålder. Vid stroke har personen drabbats antingen av en infarkt eller av en blödning i hjärnan. Restsymtomen efter en stroke kan uttrycka sig på olika vis. Vanligaste symtomen är domningar eller förlamningar i ansikte, armar och ben. Rehabilitering efter en stroke kan ta lång tid och efter sjukhusvistelsen är det ofta närstående som tar det största ansvaret för omvårdnaden av personen som drabbats av stroke. Syfte med studien var att undersöka närståendes upplevelser och erfarenheter av att vårda en person som drabbats av stroke. Litteraturöversikten genomfördes genom kritisk granskning och analys av kvalitativa och kvantitativa vårdvetenskapliga artiklar, enligt analysmodellen av Friberg (2006). Litteratursökningen gjordes i databaserna Cinahl och Pubmed. I resultatet framträdde två huvudteman : Förändrad livsvärld och Upplevelser och erfarenhet med hälso- och sjukvårdspersonal. Resultatet visade att närstående upplevde en stor livsförändring där rutiner och livsmönster ändrades och anpassades efter personen som drabbats av stroke. Det gjorde att närstående upplevde att det inte fanns tid för egna intressen. Närstående upplevde både psykisk- och fysisk ohälsa som stress, depression, ångest, högt blodtryck, magsmärtor och sömnsvårigheter. Många närstående upplevde att informationen från hälso- och sjukvårdspersonalen var otillräcklig. Det medförde att närstående kände sig osäkra på att vårda den som drabbats av stroke. Sjuksköterskor har möjlighet att påverka närståendes upplevelser genom att bemöta dem på ett respektfullt och lyhört sätt. Det handlar också om att de kan identifiera informationsbehovet för att ge adekvat information som kan stilla närståendes oro. / Program: Sjuksköterskeutbildning

Psychosocial support from family is important in outpatient treatment programs for individuals with depressive disorder. The purpose of this phenomenological study was to explore the lived experiences and perceptions of parents of patients with depressive disorder regarding intensive outpatient treatment. The research question was what are the experiences and perceptions of parents of patients with depression regarding their role as caretakers in intensive outpatient treatment? The conceptual framework was a biopsychosocial framework and family systems theory. Content analysis was used to analyze data provided from interviews with parent participants (n = 8). Many participants reported high levels of involvement with various forms of support. They maintained positive relations with professionals, were involved in patient socialization, and facilitated adherence to patients' treatment plans. The results of this study indicated that family caregivers experienced ambivalent emotions toward their roles and patients. Findings also indicated experiences of exhaustion, strong emotions about the burden of having to support the patient, and concern for their own and the rest of the family's well-being. Future researchers should study these aspects further. Researchers, clinical practitioners, and policy makers must increase efforts to support those who help family members suffering from depression to intensify the search for effective ways to reduce the toll on those caregivers. Because of these findings, researchers could expand literature to illuminate the decisions and practices of psychotherapists, leading to improvements in intensive treatment programs for both patients and their caretakers. This study impacts social change by providing insights to aid policy makers in ensuring that outpatients receive the best treatment program available and that their primary caretakers are psychologically prepared and healthy.

Caregivers (CG) often neglect their own self-care which may have deleterious effects if CG have a chronic illness, such as diabetes. Care demands have been linked to CG health, although the mechanisms are unclear. The purpose of this study was to examine the relationships of CG stress, depressive symptoms, and diabetes self-care practices on CG physical health (PH) and glycemic control (GC) in an underrepresented group of Hispanic CG with diabetes. A correlational design was used in a non-random sample of 42 Hispanic CG with diabetes (Type I or II) recruited from two health centers serving the uninsured. CG had diabetes for ≥ 6 months, were on average 48.0 (± 11.4) years old, 73.8% female, and 54.8 % with < 8th grade education. Care recipients were on average 53.9 (± 14.0) years old, 54.8 % male, and were functionally independent. Standard questionnaires for perceived caregiving stress (Caregiver Burden Scale), depressive symptoms (CES-D), diabetes self-care practices (Diabetes Care Profile), PH (PCS of the SF12v2) and CG characteristics were administered in person. GC was measured using the glycosylated hemoglobin A1c (HgbA1c). Statistical analysis included correlations, t-tests, and multiple linear regression. On average CG had poor GC (HgbAlc M = 9.0, ± 2.12), but rated their PH better than others with diabetes. CG with high stress had more depressive symptoms (M = 23.75 ± 12.75) than CG with lower stress (M = 15.75 ± 12.01; t (40) = 2.00, p = .026). Almost half (40.5%) had depressive symptoms indicating possible clinical depression. The hypothesized models of caregiver stress, depressive symptoms, and self-care practices were not associated with CG PH (p > .05) or GC (p >.05); however, more persons in the household was associated with poor GC. This study provided support for the influence of CG stress on psychological health in the experience of Hispanic CG with diabetes. The findings of high levels of depressive symptoms and poor GC suggest the need for health care professionals to assess the psychological health of Hispanic CG and better educate them about the importance of GC for prevention of serious health problems.