Дисертації з теми "Dementia support"
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Dawood, Eman Salah. "Dementia caregiving impact of location of residence on stress, coping, social support and health /." Diss., Online access via UMI:, 2007.
Знайти повний текст джерелаBennett, Claire. "Developing a tool to support diagnostic delivery of dementia." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/45188/.
Повний текст джерелаAlwin, Jenny. "Assessment of Support Interventions in Dementia : Methodological and Empirical Studies." Doctoral thesis, Linköping : Department of Medical and Health Sciences, Linköping University, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-54312.
Повний текст джерелаEngström, Maria. "A Caregiver Perspective on Incorporating IT Support into Dementia Care." Doctoral thesis, Uppsala University, Department of Public Health and Caring Sciences, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7267.
Повний текст джерелаAim: The overall aim of the present thesis was to describe and evaluate IT support in dementia care from the perspectives of staff and relatives. More specifically, it was to examine staff members’ satisfaction with work, life satisfaction and sense of coherence before and after increased IT support, to describe staff members’ opinions and perceptions of IT support during the process of implementation, to describe relatives’ opinions of IT support and to compare relatives’ perceptions of their irritations with care and life satisfaction before and after increased IT support. In addition, three questionnaires were further developed and tested among staff working in elderly care, and then used in the staff evaluation. Methods: A quasi-experimental design with baseline assessments and follow-ups and experimental and control groups was used in two studies to investigate the outcomes of IT support. A descriptive design was used to study staff views on IT support, and a correlative design was used in the methodological study. Participants were 33 staff members and 22 relatives in the evaluation, 14 staff members in the descriptive study and 299 staff members in the methodological study. Data collection methods were questionnaires and group interviews. The IT support consisted of passive passage alarms, fall detectors, sensor-activated night-time illumination of the lavatory, movement detectors, email communication, an Internet website and additional computers. Findings and conclusions: Staff job satisfaction and perceived quality of care increased in the experimental group. The relatives were generally positive about the IT support, and the experimental group showed a decrease in practical/logistical irritations. Staff described ‘moving from fear of losing control to perceived increase in control and security’ and ‘constant struggling with insufficient/deficient systems’. Conclusions are that IT support can be a resource in dementia care as perceived by caregivers if IT support is incorporated into the care system.
Lindgren, Helena. "Decision support in dementia care : developing systems for interactive reasoning." Doctoral thesis, Umeå : Datavetenskap Computing Science, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1138.
Повний текст джерелаBennasar, Mohamed. "Clinical decision support system for early detection and diagnosis of dementia." Thesis, Cardiff University, 2014. http://orca.cf.ac.uk/73073/.
Повний текст джерелаO'Rourke, G., C. Pentecost, den Heuvel E. van, C. Victor, Catherine Quinn, A. Hillman, R. Litherland, and L. Clare. "Living with dementia during the COVID-19 pandemic: coping and support needs of community-dwelling people with dementia and their family carers. Research findings from the IDEAL COVID-19 Dementia Initiative (IDEAL-CDI)." Older People and Frailty Policy Research Group, 2021. http://hdl.handle.net/10454/18452.
Повний текст джерелаWe interviewed people with dementia and carers from the IDEAL cohort to find out how the COVID-19 lockdown and continuing restrictions affected those living with dementia. Some people with dementia coped well, while others coped with difficulty or were only just coping. The additional stress of COVID-19 exacerbated pre-existing coping difficulties. For many, social isolation increased anxiety. Some felt that lack of activity or lack of social contact caused a decline in their abilities to manage everyday tasks. Confusion about COVID-19 rules or difficulty remembering what to do led to anxiety when leaving the house. People felt that members of the public might not understand their particular needs. While some carers felt they were coping well, others experienced stress when having to leave the home because the person with dementia might not be safe if left alone. Some experienced increased strain in the caring relationship compounded by an uncertainty about future availability of respite. Some were concerned about the complex health needs of the person with dementia alongside COVID-19 risk and lack of personalised information. Both people with dementia and carers talked about the importance of access to safe outdoor space. People were anxious about how others would react or behave towards them regarding keeping a distance if they went out. Being connected to friends, family and wider community or support groups was important to help combat the effects of isolation. People from BAME communities worried about their increased vulnerability to the virus. A lack of trust in Government guidance and in health care services added to their anxiety. However, some benefitted from strong community and faith group involvement. What might be helpful for people with dementia? • Reablement to help regain or maintain skills • Personalised health advice regarding managing COVID-19 risk and the opportunity to ask questions. • Identification of people with dementia who live alone and an assessment of their needs. What might be helpful for carers? • Needs assessment in regard to respite. • Novel forms of respite care that incorporate social distancing. What might be helpful for both carers and people with dementia? • Access to COVID-safe outdoor spaces. • Continuation and expansion of ‘just checking’ services. • Support to get online and use the internet. • Communication and information through non-digital means. • Community COVID-19 ‘dementia awareness’ initiatives. What might be helpful for people from Black and minority ethnic groups? • Addressing concerns about their increased risk of COVID-19. • Directing information and support through existing community and faith groups.
This report presents independent research funded by the National Institute for Health Research Policy Research Unit in Older People and Frailty.
Ottenby, Anki. ""När jag väl har friheten…" : - en kvalitativ studie om anhörigas upplevelse av stöd." Thesis, Stockholm University, Department of Social Work, 1998. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-26251.
Повний текст джерела
With this study I wanted to capture the experience of support and increase the knowledge of what it means for women who are living with a husband who suffers from dementia. To do so I conducted four interviews and used an informal questionnaire. The result shows that there are four key words that can symbolize what the women experience as support: communica-tion, freedom, understanding and knowledge. The women’s experience of support range from meaningful and secure to not satisfying and complicated. Living with a husband who suffers from dementia has made their lives very different from before. But even if they sometimes are in a tough situation they want to take care of their husbands. Being able to go away a few hours or half a day once a week, can sometimes be enough and gives the women a sense of satisfaction. On the other hand it is not certain that the support offered is what the women need or that it is satisfactory for the husband. The link between the women’s experience of support and that of their husband is strong. And if the husband is not pleased nor will the wife be.
Egdell, Valerie. "The changing landscape of informal dementia : mapping the sites, stages and support." Thesis, University of Newcastle Upon Tyne, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.512135.
Повний текст джерелаMarshall, Ann. "Coping in early dementia : findings of a new type of support group." Thesis, University of Surrey, 1999. http://epubs.surrey.ac.uk/712/.
Повний текст джерелаTzimoula, X. M. "Social support and psychological health of family carers of people with dementia." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1418834/.
Повний текст джерелаBartels, Lucy. "Understanding positive experiences of professional caregivers who support people living with dementia." Thesis, University of Hull, 2017. http://hydra.hull.ac.uk/resources/hull:15912.
Повний текст джерелаDokos, Malinda K. "The Role of Social Support in Dementia Care Facilities: Staff Member Perspectives." DigitalCommons@USU, 2019. https://digitalcommons.usu.edu/etd/7648.
Повний текст джерелаAndersson, Liza, and Lovisa Axelsson. "Att vara närstående till en äldre person med demenssjukdom : En litteraturstudie med kvalitativ ansats." Thesis, Högskolan Väst, Avdelningen för omvårdnad - grundnivå, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-10624.
Повний текст джерелаBackground: Dementia not only affects the individual patient, but also healthcare professionals and the relatives. It is an increasing incurable disease that affects the mind of the afflicted person. He or she will experience difficulties with either expressing oneself, recognizing daily things, performing tasks that he or she previously were able to managed or the ability to plan, initiate or complete various tasks. Aim: The aim of this study was to illuminate experiences of being a relative of an older person afflicted of dementia. Method: A literature based study was performed, analyzing 10 qualitative articles. Results: The results consist of two main themes, relatives experiences of support, with two subthemes, support in the care relationship and support from others in the same situation. The second theme progression of the disease and its affects on relations and feelings, with three subthemes, the partners behavioral change, a new kind of relationship and impact of the disease on feelings. These highlight significant experiences the relatives go through in relation to the disease. Support was something that may be given in different ways and the need for support was necessary. The behavioral change that comes with the disease, results in a new form of relationship with the affected. Feelings of sadness, guilt and shame were constantly present. Conclusion: The results shows that the relatives need support through the entire disease progression when the behavior of the affected changes and a new relationship is formed. When accepting the disease, the relatives found it easier to deal with life in general. Nurses need to have the means to respond to these relatives and to know how they experience their situation, to be able to support them in the best possible way.
Kjällman, Alm Annika. "Long-Term Ongoing Structured Support in Early Stage of Dementia: A Family Affair." Doctoral thesis, Mittuniversitetet, Avdelningen för omvårdnad, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:miun:diva-22673.
Повний текст джерелаDementia disorders affect more than 35 million people around the world, which will double every twenty years. Dementia is a global disruption of intellectual functioning; there is a decrease of memory ability and other intellectual abilities such as orientation, visuospatial- perceptive ability, language, thinking, executive abilities, problem solving, apraxia and agnosia. These symptoms are often followed by behavioral changes and changes in the personality, such as loss of initiative, emotional instability, irritation, apathy, coarse social behaviour and mood changes. The most frequent symptoms were apathy, depression, irritability, and agitation. About 25, 000 persons are diagnosed with dementia each year in Sweden. Today, estimates are that 160, 000 persons in total are suffering from dementia in Sweden. In Sweden, most diagnoses are done in the primary health care setting by general practitioners and are based on the person´s own history, interviews with next of kin and an Mini Mental Score Evaluation- Swedish Revision (MMSE-SR) along with blood work and a brain scan to rule out any other diseases. After diagnosis the next of kin often have many questions about the coming lifestyle changes and ways to handle the personality changes that the person suffering from dementia may go through. Previous studies show that in many cases these questions are left unanswered, because it is difficult to get a follow up with a physician and there are few countries where support after diagnose is common. In 2009, the Swedish Parliament passed a new law that states that support is to be given to persons caring for people with chronic illnesses, elderly people, or people with functional disabilities. There was, however, no detailed description of the extent or kind of services to be provided, and the municipalities had extensive freedom in implementing the legislation. In the autumn of 2013 the Swedish National Health Board therefore, issued guidelines where eight to ten meetings during a three- to six-month period with information and social support were recommended.A municipality in northern Sweden have a long term ongoing support to persons with dementia and their next of kin since 2006. A close collaboration with the geriatric clinic and private health centers has resulted in support being offered within 4-6 weeks after diagnose. The overall aim of this thesis was to explore experiences of living with dementia both as a sufferer and as a next of kin; and being part of a long-term ongoing support group, the longest for four years. Interviews were done with persons with dementia and their next of kin. Results showed that couples who had been the longest in a support group felt great comfort and support. They experienced that their knowledge about the disorder was good and that they could prepare for the changes to come. Results also showed that to be an adult child of a person with dementia disease means being burdened with the responsibility to act on behalf of the diseased parent despite a deep sense of grief and loss, which leads to frustration with the situation. Relationships within the family can sometimes change when a family member is affected by dementia. Sometimes for the better; where the family rallied to support the affected member and sometimes for worse; where the relationships were strained when pressure became too much. The persons with dementia who participated in the support groups experienced a great sense of coherence and felt that life was manageable, comprehensible and meaningful. Their healthy partners experienced less comprehensibility and manageability and the adult children more meaningfulness. The results of the thesis have founded a model for support called PER-model®; Pedagogical, Emotional and Relationship based model of support.
Furlini, Linda. "Living with chronic dementia from the caregiver perspective : a case for educational support." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=85161.
Повний текст джерелаMcKechnie, I. V. "The impact of an online support forum for carers of people with dementia." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1410117/.
Повний текст джерелаWherton, Joseph P. "Exploring the requirements for technology to support people with dementia in the home." Thesis, University of York, 2008. http://etheses.whiterose.ac.uk/14201/.
Повний текст джерелаWebster, Gemma. "Multimedia profiles as external personalities to support people with dementia and their carers." Thesis, University of Dundee, 2011. https://discovery.dundee.ac.uk/en/studentTheses/f68f7545-c3af-427d-b4fe-96633824208a.
Повний текст джерелаGolden-Kreutz, Deanna Maria. "Social networks, support perceptions, and depressive symptomatology in dementia family caregivers and noncaregivers /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487844948077746.
Повний текст джерелаFOX, MARY VYN. "SOCIAL SUPPORT AND PSYCHOLOGICAL DISTRESS AMONG SPOUSE CAREGIVERS OF DEMENTIA PATIENTS (ALZHEIMER'S DISEASE)." Diss., The University of Arizona, 1986. http://hdl.handle.net/10150/188184.
Повний текст джерелаEarnheart, Kristie. "Cardiovascular Problems as a Predictor of Later Cognitive Decline: Moderating Effect of General and Spousal Social Support." Thesis, University of North Texas, 2006. https://digital.library.unt.edu/ark:/67531/metadc5377/.
Повний текст джерелаGideon, Clare A. "SOCIAL ENVIRONMENTS OF DEMENTIA CAREGIVERS: RELATIONSHIPS BETWEEN SOCIAL SUPPORT, NEGATIVE SOCIAL INTERACTIONS, AND CAREGIVER EMOTIONAL DISTRESS." online version, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1158541315.
Повний текст джерелаAlbinsson, Lars. "A Palliative Approach to Dementia Care : Leadership and organisation, existential issues and family support." Doctoral thesis, Uppsala University, Department of Public Health and Caring Sciences, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2930.
Повний текст джерелаThe main purpose of this thesis was to apply the WHO and NHS palliative care approach to dementia care.
Thirty-one staff-members in mid-Sweden (studies I and II) and 20 next-of- kin (study IV) were interviewed. In study III, 316 staff-members from dementia care and 121 staff-members from palliative cancer care responded to a questionnaire about family support. The interviews were tape-recorded and analysed with a qualitative phenomenographic (I and II) and a hermeneutic approach (IV). The questionnaires (III) were analysed using qualitative and quantitative content analysis.
The staff-members stated almost unanimously that daily leadership was lacking, and consequently clear goal formulations and care planning were rare (I). Proper teamwork between the doctor and the staff who worked on a daily basis with the patients was absent (I). With respect to existential issues, education and staff discussions were lacking (II). The staff were at a loss concerning how to deal with these issues. Nevertheless, these issues are central to family-members who have to deal with an existential crisis (IV). Important questions emerged about obligation and guilt, faithfulness, responsibility, and paying back what you once received. Existential isolation could be identified e.g. in the reversal of roles experienced as "being a parent to your parent" and in the burden of "visiting a living dead person".
There were no routines for bereavement visits. The type of support suggested for dementia family members is partly similar to support in palliative cancer care, but it also differs in other respects such as feelings of guilt because the early signs of the disease are misunderstood, the need for respite because of the long trajectory of dementia diseases, and the occurrence of anticipatory grief because in the late phase family members can no longer make any contact at all with the patient (III).
A palliative approach can improve the quality of life for the dementia patient and for the family. It can be used as a basis for a clear goal formulation. Some of the suggestions listed in this thesis for improving the quality of care are more a reflection of the need for a change in attitudes rather than the need for substantial budget increases.
Nasrollahzadeh, Yalda. "Support group for caregivers of older adults affected by dementia| A grant proposal project." Thesis, California State University, Long Beach, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=1523109.
Повний текст джерелаThe purpose of this study was to explore how caregivers of patients with dementia are physically and mentally affected by their increase in responsibilities. The purpose of this project was to locate a potential funding source and write a grant to obtain funding for a caregiver support group for the Calabasas, CA community and its surrounding areas.
Caregiver intervention programs have been identified as a critical area of research by the Alzheimer's Association. Silverado Senior Living is a national organization that serves patients with dementia. The program consists of two support groups offering structure and flexibility through cognitive behavioral practices and a continuous feedback.
If funded and implemented, this program would add value to the body of research that exists for caregivers and drive awareness and change to current policy. In addition, Silverado would better serve its community and act as a model program for other Silverado locations.
The actual submission and/or funding of this grant was not a requirement for the successful completion of the project.
Bajaj, Preeta. "Physical environmental cues that support activities of residents with dementia in special care units." [Gainesville, Fla.] : University of Florida, 2003. http://purl.fcla.edu/fcla/etd/UFE0001080.
Повний текст джерелаChung, Yin-kwan Carol. "Stress, appraisal, coping and perceived social support as predictors of mental health outcomes of spouse-caregivers of persons withdementia." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1998. http://hub.hku.hk/bib/B29697888.
Повний текст джерелаThunberg, Julia. "Vårdpersonalens behov av stöd i sitt arbete med vårdtagarna i demensboende." Thesis, Uppsala universitet, Sociologiska institutionen, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-216137.
Повний текст джерелаDenna studie skall undersöka om vårdpersonalen, som arbetar med vårdtagare med demensproblematik, är i behov av stöd och på vilket sätt de då ser att detta i så fall ska utformas. Tidigare forskningsresultat visar att det finns väldigt många faktorer inom äldreomsorgen, som påverkar vårdpersonalen. Att arbeta med människor i denna beroendeställning kräver väldigt mycket av vårdpersonalen, både psykiskt och fysiskt. För att undersöka om vårdpersonalen anser sig ha ett behov, och i så fall på vilket sätt de ser att detta ska utformas, gjordes en kvalitativ studie. Studien delades upp i olika former av intervjuer. Det genomfördes två enskilda intervjuer och en fokusgruppintervju. Intervjuerna gjordes med sjuksköterska och chefen för demensboendet. Fokusgruppen genomfördes med fyra av demensboendets undersköterskor. Resultatet påvisar att det finns ett behov av stöd för vårdpersonalen. Ett arbete på ett äldreboende, med inriktning för vårdtagare med demensproblematik innebär dagligen svårigheter, vissa mer svårhanterliga än andra. De mer svårhanterliga utmaningarna, som sker på demensboendet, behöver vårdpersonalen hjälp att hantera. Stödet får gärna vara utformat i både interna och externa former, som till exempel stöd mellan kollegor och handledning. Det framkommer även av vårdpersonalen att de behöver ett stöd i sitt arbete trots flera års erfarenhet. Behovet av kontinuerlig kompetensutveckling ligger, enligt vårdpersonalen, i att varje vårdtagare har olika behov. Det kan ses som liknande behov, men det är aldrig helt lika.
LIU, YU. "Impact of Family Caregiving upon Caregivers of Elders with Dementia in China." Diss., The University of Arizona, 2010. http://hdl.handle.net/10150/193869.
Повний текст джерелаAtcha, Maaria. "Access to dementia diagnosis and support in a diverse South Asian community : a qualitative study." Thesis, Lancaster University, 2018. http://eprints.lancs.ac.uk/127056/.
Повний текст джерелаChristie, Julie. "'I try to forget about the dementia' : realising the resilience of the person ageing with dementia in social work practice." Thesis, University of Stirling, 2016. http://hdl.handle.net/1893/24422.
Повний текст джерелаPennington, Sarah C. E. "A longitudinal investigation into the effect of social support on depression and anxiety in dementia caregivers." Thesis, University of East Anglia, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.426812.
Повний текст джерелаLett, Judy. "Utilization and evaluation of formal support services among informal caregivers of non-institutionalized elderly with dementia." Thesis, McGill University, 1994. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=55508.
Повний текст джерелаResults indicated that formal support service users cared for demented elderly who had greater ADL/IADL functional limitations, reported more burden, tended to be husbands, tended not to live with the care recipient, reported less informal support, and tended to live in the Prairie region. They also tended to perceive their health to be better than a year ago. Service users' reports indicated that utilization of in-home services was considerably greater than that of out-of-home services. Out-of-home respite and caregiver support groups had the largest number of barriers to use. The most common barriers identified for all services included cost and perceived lack of effectiveness.
Edwards, Angela Catherine. "An Evaluation of a Specialist Multi-Agency Home Care Support Service for Older People with Dementia." Thesis, University of Nottingham, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.517848.
Повний текст джерелаPenny, Katherine Elizabeth. "The use of Telecare to support people with dementia to remain living in their own homes." Thesis, University of Southampton, 2018. https://eprints.soton.ac.uk/422201/.
Повний текст джерелаDouglas, Lorraine. "Stress, coping and self-efficacy : designing an intervention to support informal caregivers of people with dementia." Thesis, Heriot-Watt University, 2017. http://hdl.handle.net/10399/3352.
Повний текст джерелаMay, Auriel Adele. "A person-centred AAC intervention to support interpersonal interaction in persons with dementia : an exploratory study." Thesis, University of Pretoria, 2020. http://hdl.handle.net/2263/78801.
Повний текст джерелаThesis (PhD)--University of Pretoria, 2020.
Sponsor 1: National Institute for the Humanities and Social Sciences (NIHSS), in collaboration with the South African Humanities Deans Association (SAHUDA). Opinions expressed in this report and conclusions arrived at are those of the author and are not necessarily to be attributed to the NIHSS and SAHUDA. Sponsor 2: Andrew W. Mellon Foundation
Centre for Augmentative and Alternative Communication (CAAC)
PhD
Unrestricted
Elliott, Ryan M. "The effect of prolonged support group attendance on depression among family caregivers to patients with dementia." Online version, 1999. http://www.uwstout.edu/lib/thesis/1999/1999elliott.pdf.
Повний текст джерелаNordström, Sanne, and Rebecka Persson. "Stöd när minnet sviker : Stöd för person med demenssjukdom." Thesis, Högskolan i Halmstad, Sektionen för hälsa och samhälle (HOS), 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-22195.
Повний текст джерелаProblem: The research on support for people who have received themedical diagnosis of dementia is inadequate. Also, how different care teamswith nurses may use the support, prescribe independently and get prescribeddependent care measures need to be identified and developed. Whatkind of support is offered directly to and how can the nurse supportpeople with dementia diagnosis.Aim: The aim was to highlight the support for people with dementia.Method: The study was conducted as aliterature review and was based on 15 scientific articles. These were reviewed,analyzed and categorized in order to find support for people with dementia. Results and Conclusion: The results revealedsix categories that generate support for persons with the medical diagnosis ofdementia: ”Needs and support”, ”Subjective experience of support for peoplewith dementia”, ”Support-groups and compounds”, ”Education of caregivers”,”Tools” and ”Surrounding and environment”. Implication: Further research concerningsupport for people with dementia from a subjective perspective is needed for abetter understanding of what support is for people with dementia.
Abika, Angela, and Evakajsa Jönsson. "Hur gör jag för att orka? : Stöd till närstående som vårdar en demenssjuk i hemmet." Thesis, Högskolan i Borås, Akademin för vård, arbetsliv och välfärd, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-11975.
Повний текст джерелаRussell, Alexandra. "Using life story boards to engage clinical support workers in person-centred care with people living with dementia in an NHS Inpatient Dementia Care Unit : a thematic analysis." Thesis, University of East Anglia, 2016. https://ueaeprints.uea.ac.uk/60986/.
Повний текст джерелаHamal, Pragya. "Evidenced-Based Support Services for Informal Caregivers of Individuals with Dementia in the United States, India, and Nepal." Bowling Green State University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1403796240.
Повний текст джерелаJude, Caroline. "Depression, anxiety and social support of caregivers for people with dementia living at home or in residential care." Thesis, University of East Anglia, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327202.
Повний текст джерелаBrooks, Deborah Jane. ""Bereavement without death": Improving psychosocial support of spousal family carers of people with dementia following placement into residential care." Thesis, Queensland University of Technology, 2020. https://eprints.qut.edu.au/201748/1/Deborah_Brooks_Thesis.pdf.
Повний текст джерелаSmith, Hinders Julie Ann. "Unmet Support Needs of Informal Caregivers of Older Adults." ScholarWorks, 2019. https://scholarworks.waldenu.edu/dissertations/6375.
Повний текст джерелаSiverth, Emelie, and Sandra Levisson. "Sjuksköterskors stöd till anhöriga som vårdar personer med demens : En litteraturöversikt." Thesis, Jönköping University, HHJ, Dep. of Nursing Science, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-6567.
Повний текст джерелаUppskattningsvis lever 24 miljoner personer med en demenssjukdom idag, en siffra som förväntas öka. En demenssjukdom innebär ett lidande för personer med demens eftersom de som drabbas får svårigheter att sköta sitt dagliga liv. En demenssjukdom innebär också ett lidande för anhöriga. Över hela världen utför anhöriga den största delen av omvårdnaden för personer med demens. Anhöriga till personer med demens bär ofta ett stort ansvar och upplever sig psykiskt belastade, övergivna och i behov av stöd. Syftet med den här studien var att undersöka sjuksköterskors stöd till anhöriga som vårdar personer med demens. Studien genomfördes som en litteraturöversikt där 14 vetenskapliga studier granskades och analyserades. Huvudfynden visar att sjuksköterskorna gav både individbaserat och gruppbaserat stöd genom individuella behovsbedömningar, emotionellt och socialt stöd, samt stöd genom undervisning och information. Oavsett vilken typ av stödåtgärd som användes tycktes uppmärksamheten på och engagemanget för anhöriga vara det viktigaste stödet. De olika typerna av stödåtgärderna ledde till att anhöriga fick ökade färdigheter i omvårdnaden och till att anhörigas psykiska hälsa förbättrades. Det sågs att det är en viktig del i sjuksköterskornas arbete att uppmärksamma anhörigas behov, vara medvetet närvarande i mötet med dem och visa ett aktivt engagemang för dem.
Approximately 24 million people are living with a dementia disease today, a number which is expected to increase. A dementia disease entails suffering for persons with dementia because they experience difficulties in their daily life. A dementia disease also entails suffering for the relatives. All over the world the relatives are largely responsible for the caring of persons with dementia. Relatives to persons with dementia often carry a great deal of responsibility and a feeling of psychological burden, abandonment and they are in need of support. The aim of this study was to investigate how nurses can support the relatives caring for persons with dementia. A literature review was used where fourteen scientific articles were investigated and analyzed. The main findings showed that nurses gave both individually based and group based support through individual needs assessment, emotionally and social support, as well as support by teaching and information. Irrespective of the type of intervention it was the nurses´ attentiveness on and their commitment for the relatives that was the most important support. The different types of interventions resulted in that the relatives gained increased caring potential and experienced improved mental health. It was noticed that an important part of nurses´ work is to be attentive to the relatives´ needs, being consciously aware in the meeting with them and showing an active attentiveness for them.
Eklund, Emelie, and Andersson Lovisa Lundberg. "Distriktssköterskans erfarenheter av att stödja närstående som vårdar en person som insjuknat i demens." Thesis, Linnéuniversitetet, Institutionen för hälso- och vårdvetenskap (HV), 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-53627.
Повний текст джерелаBackground: Dementia is described as a disease that affects the whole family, whereof relatives are taking a considerable part of the caring in the home. As a consequence the related person can experience a negative impact on the physical as well as the psychological health. To be able to give good support the district nurse’s ability to read the related’s and the patient’s needs is of great importance. However, there are difficulties in the district nurse's work to meet the needs of related parties as well as to be an optimum support. Purpose: The purpose of the study was to describe the district nurse’s way of working and abilities as well as problems in supporting relatives who’s taking care of individuals with dementia. Method: The study was conducted as an interview study with semi-structured interviews. The method was qualitative with an inductive approach. Expedient selection was applied in the recruitment of participants. The inclusion requirement were district nurses in home care from two municipalities in southern Sweden, with intermediate or greater experience in the field. The content of the interviews were analysed using qualitative latent content analysis, as described by Graneheim och Lundman (2004). Result: The result includes nine categories with associated subcategories. The following categories were created; “The district nurse wants to originate from a holistic perspective”, ”The district nurse wants to work preventively through sustained contact with related parties”, “Becoming engaged late is a barrier in health promotion”, “Team collaboration creates conditions for the district nurse to provide support to related parties”, ”A mutual relationship can support related in the care process”, “Paying attention to and be responsive to related parties need of support”, “Opportunities to meet the needs of support is complicated by related parties' inability to accept help” and “Promoting the district nurse's ability to pay attention to related parties’ need off support”. These categories fell under two themes; “Staying ahead to meet the whole human” and “To be available and responsive to the desires of patients and related”. Conclusion: There were differences in using or not using procedures between the municipalities. The district nurses use several methods to support related who’s taking care of individuals with dementia, but feel that they are sometimes engaged late, which prevents them from providing health promotion and optimal care. The district nurses wished for routines, more education in the area as well as tools that could facilitate their work to highlight and identify related persons support needs and wellbeing.
Jönsson, Hanna, and Anna Matilainen. "Sambandet mellan sorg, coping och stöd. En kvalitativ undersökning om anhöriga till yngre personer med demens." Thesis, Malmö högskola, Fakulteten för hälsa och samhälle (HS), 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-26401.
Повний текст джерелаDementia is often age related and develops in a late stage of life but people can fall ill in a younger age. The roll of the close relative can be both psychologically and physically wearisome and hence important to emphasize on. The aim of the study was to explore the complex qualitative connection between the components grief, coping strategies and support among close relatives to a person developing dementia in a young age. Qualitative interview study method was used with semi structured interviews using an interview guide. Qualitative content analysis was applied. There is an interrelated connection between the three components, with the support as the foundation. A discovered central theme is the searching for security as this is a necessity for the grieving process ability. A satisfying support can enhance the external context and compensate for the insecurity the close relative experiences in this altering situation. The extent of the secure external context influences the chosen coping strategies by the affected close relatives. This study provides insight into the emotional situation of a close relative of a person who is developing dementia. A connection between the components have been found and described. The understanding of this connection could potentially be applied in other areas within social work and hence guide the chosen actions and support to create a more manageable everyday life for the client.
Djapo, Hanna. "Närstående till äldre med demenssjukdom och deras upplevelser av stöd på äldreboenden : en kvalitativ studie." Thesis, Sophiahemmet Högskola, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:shh:diva-1370.
Повний текст джерелаDukart, Jürgen. "Contribution of FDG-PET and MRI to improve Understanding, Detection and Differentiation of Dementia." Doctoral thesis, Universitätsbibliothek Leipzig, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-66495.
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