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As the baby boomer generation ages, and as advanced medical techniques keep people alive longer, the need for family caregivers will grow. Researchers have determined that the health of family caregivers is generally poorer that noncaregivers. Also, the type of family relationship has been determined to influence health outcomes. This study examined how caregiving parents and caregiving adult children compared with regard to caregiving variables and health outcomes. Social support was then assessed to determine if a mediating effect existed between the predictors and health outcomes. Using data from the MIDUS II survey, the health outcomes of self-identified caregiving parents and caregiving adult children was studied in light of the predictor variables of type of relationship, provision of activities of daily living, length of time caregiving, and family demands. Multiple regression analysis was used to determine the relation between the predictors and health outcomes. Mediation tests were administered to assess if social support mediated between the significant predictors and health outcomes. The type of family relationship influenced health outcomes with caregiving parents demonstrating poorer health than caregiving adult children. Caregiving parents had lower self-rated health and higher numbers of chronic conditions than caregiving adult children. Perceived family demands were associated with increased number of chronic conditions for both caregiving adult children and caregiving parents. No significant influence was found between provision of activities of daily living or length of time caregiving with health outcomes. Similarly, no mediation effect of social support was found between the significant predictor variables and health outcomes. Using the stress process model, this study examined caregiving predictor variables and health outcomes for caregiving parents and caregiving adult children. Caregiving parents were found to demonstrate poorer self-rated health and more chronic health conditions that caregiving adult children. Unlike many previous studies, perceived family demands was found to have a strong association with the number of chronic health conditions for both groups of caregivers. / Graduation date: 2012

Thesis--University of Oklahoma. / Bibliography: leaves 71-73.

Thesis (M.S.)--University of Michigan, 1992.

Thesis (M.N.)--Memorial University of Newfoundland, 1998. / Bibliography: leaves 123-132.

Thesis (M.S.)--University of Michigan, 1992.

With the increasing elderly population and longer life expectancies, smart wearable technologies are playing an important role in facilitating caregivers to monitor elderly people remotely. Aifloo’s wristband is one smart wristband which can collect various data, predict activities and detect abnormalities to enable elderly people to live independently at home. However, too much information and poor visualizations will cause huge difficulties for caregivers to interpret the data. Six caregivers were interviewed in this study to investigate what data is relevant to monitor elderly people and how they interpret the different designed displays. The main results show that alarms, fall incidents and medication compliance are the most important. Besides, caregivers place a greater emphasis on holistic views of data and they want to highlight abnormal behaviors and alerts. In the end, design guidelines for the information system to present data meaningfully and intuitively are generated. / Med ett ökande antal äldre och en ökande medellivslängd kommer smart, bärbar teknologi att spela en större roll i äldrevården för att övervaka de äldre. Aifloos armband är en smart teknologi som kan samla in olika former av data, förutsäga aktiviteter och upptäcka avvikande och onormala beteenden, vilket kan användas av äldre som bor självständiga i sena egna hem. Stora mängder data, och dåliga visualiseringar av dem, orsakar svårigheter för vårdgivare att tolka datan. I den här studien har sex vårdgivare intervjuats för att utforska vilken data som är relevant för dem, och hur de kan tolka information ifrån en grupp olika gränssnitt. Studiens resultat visar att alarm, fallolyckor och översikt över hur de äldre efterföljer sina medicinska recept är viktigast. Vårdgivarna lägger en större vikt vid att förstå datan holistiskt, och de vill synliggöra avvikande beteendemönster och varningar. Slutgiltligen presenteras riktlinjer för hur IT-system kan designas för att presentera data på ett meningsfullt och intuitivt vis.

"June 2002" / Bibliography: p. 347-360. / xiii, 360, [200] p. : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (M.Med.Sc.)--University of Adelaide, Dept. of Public Health, 2002

Submitted by Noeme Timbo (noeme.timbo@metodista.br) on 2017-04-24T18:37:50Z No. of bitstreams: 1 ANA LUIZA DIAS.pdf: 998026 bytes, checksum: 04c1ef7903cb5ba7c64bf646198de914 (MD5) / Made available in DSpace on 2017-04-24T18:37:50Z (GMT). No. of bitstreams: 1 ANA LUIZA DIAS.pdf: 998026 bytes, checksum: 04c1ef7903cb5ba7c64bf646198de914 (MD5) Previous issue date: 2016-03-18 / Cancer is the main pathology responsible for deaths among children and adolescents in Brazil and the estimate shows that there is a growing incidence of new cases year after year. The treatment for this chronic disease is long, painful and distressing and the possibility of death follows the patient and family all the time in this process. Besides, the health care network in many regions of our country is not prepared to provide the necessary services for this population, therefore, children and caregivers are transferred to cancer centers of reference which are often indeed far from their homes. Therefore, the objectives of this study are aimed at the description of the health beliefs of caregivers of children with cancer welcomed by support houses of São Paulo and to understand the influence that this health beliefs have on the role of caregiver. 10 women were interviewed, mostly mothers of infants aged from 04 to 13 years who were under treatment for cancer or in remission and control period. The collected data were analyzed according to the research model in "health beliefs" which assesses the impact of the diagnosis, susceptibility, severity, benefits, barriers, self-efficacy and expectations for the future according to the perception of each caregiver. The results show that from diagnosis until the last visit of the control period anguish, anxiety, insecurity and fear are present in the routine of these women and the distance of their homes, the extended family and their everyday activities is a factor that significantly aggravates the intense suffering that this experience cause. From these results it is recommended that more psychosocial care from multidisciplinary teams of support houses and health care network in order to lessen the emotional burden and reduce the psychological damage caused by cancer and their processing. It is expected that changes in this area allow families a better living with the disease and the inevitable transfer to oncology centers, as well as re-establish basic aspects of quality of life of children cancer patients caregivers. / O câncer é a principal patologia responsável por óbitos entre crianças e adolescentes do Brasil e a estimativa mostra que haverá uma crescente incidência de novos casos ano após ano. O tratamento para esta doença crônica é longo, doloroso e angustiante e a possibilidade de morte segue o paciente e a família o tempo todo neste processo. Além disso, a rede de assistência à saúde de muitas regiões do nosso país não está preparada para prestar os serviços necessários para esta população, sendo assim, crianças e acompanhantes são transferidos para centros oncológicos de referência que muitas vezes ficam deveras distantes de seus lares. Portanto, os objetivos deste estudo visam à descrição das convicções de saúde das cuidadoras de crianças com câncer acolhidas por casas de apoio da cidade de São Paulo, bem como à compreensão da influência que estas convicções de saúde exercem no papel de cuidador. Foram entrevistadas 10 mulheres, em sua grande maioria mães, de infantes com idade entre 04 e 13 anos que estavam sob o tratamento contra o câncer ou em período de remissão e controle. Os dados levantados foram analisados de acordo com o modelo de pesquisa em “convicções de saúde” que avalia o impacto do diagnóstico, a suscetibilidade, a severidade, os benefícios, as barreiras, a eficácia própria e as expectativas para futuro segundo a percepção de cada cuidador. Os resultados apontam que desde o diagnóstico até a última consulta do período de controle a angústia, a ansiedade, a insegurança e o medo estão presentes na rotina destas mulheres. Também, o distanciamento de seus lares, dos familiares e de suas atividades corriqueiras é um fator que agrava significantemente o sofrimento intenso que esta experiência causa. Diante destes resultados recomenda-se mais atenção psicossocial das equipes multidisciplinares das casas de apoio e da rede de assistência à saúde com o propósito de diminuir a carga emocional e reduzir os danos psíquicos causados pelo câncer e seu respectivo tratamento. Espera-se que mudanças neste âmbito possibilitem às famílias um melhor convívio com a doença e a inevitável transferência para outros centros de atendimento, bem como restabeleça aspectos fundamentais da qualidade de vida de cuidadores de pacientes oncológicos infantis.

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