Thematische Bibliographien / Care of disabled people

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Dissertationen
Bücher
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Konferenzberichte
Berichte der Organisationen

Auswahl der wissenschaftlichen Literatur zum Thema „Care of disabled people“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 20. Februar 2023

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Zeitschriftenartikel zum Thema "Care of disabled people"

Dewing, Jan. „Physically disabled people in acute care“. Nursing Standard 5, Nr. 22 (20.02.1991): 37–39. http://dx.doi.org/10.7748/ns.5.22.37.s43.

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SARMAH, A. „Transitional care of young disabled people“. Archives of Disease in Childhood 81, Nr. 2 (01.08.1999): 189. http://dx.doi.org/10.1136/adc.81.2.189d.

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Albrecht, Gary L. „Rationing health care to disabled people“. Sociology of Health and Illness 23, Nr. 5 (September 2001): 654–77. http://dx.doi.org/10.1111/1467-9566.00270.

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Grata, Paweł. „The Social Policy of the Second Polish Republic Towards Disabled People“. European Journal of Multidisciplinary Studies 5, Nr. 1 (19.05.2017): 420. http://dx.doi.org/10.26417/ejms.v5i1.p420-424.

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Problems of disable people were a very important social issue in the Second Republic of Poland. Social policy towards them was not unitary. It dealt with issues of war invalids (veterans and civilians), casualties of work accidents (who were insured) and poor disabled people (uninsured). A legal basis for these activities of the state and local governments was different and the support for the particular groups of disabled people was also various. The war invalids received more support than others. The help involved e.g. pensions, health care, prostheses and a chance to get a job. The casualties of work accidents received pensions and health care but their benefits were fewer than benefits for war invalids. Poor disabled people were in the worst position. The state, local governments, charity organisations tried to help them but their possibilities were too small in relation to the needs. Poor disabled people received neither benefits nor health care, they could not expect the help in retraining and finding a job and only few of them could count on a place in care facility (the number of these places was too small).

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Aitken, C., und J. Walker. „Care of disabled people in the community“. International Disability Studies 9, Nr. 2 (Januar 1987): 60–61. http://dx.doi.org/10.3109/03790798709166236.

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Barnes, Colin. „Institutional discrimination, disabled people and interprofessional care“. Journal of Interprofessional Care 8, Nr. 2 (Januar 1994): 203–12. http://dx.doi.org/10.3109/13561829409010420.

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Dyer, C. „Disabled people take care issues to court“. BMJ 310, Nr. 6994 (17.06.1995): 1555. http://dx.doi.org/10.1136/bmj.310.6994.1555.

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Wu, Danxian, Xiaolu Gao, Zhifei Xie und Zening Xu. „Understanding the Unmet Needs among Community-Dwelling Disabled Older People from a Linkage Perspective“. International Journal of Environmental Research and Public Health 18, Nr. 2 (06.01.2021): 389. http://dx.doi.org/10.3390/ijerph18020389.

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One of the challenges in response to population aging is to meet needs for elderly care among older people especially for those who want to age in their homes or communities. However, disabled older people have more challenges due to their restricted mobility to access care resources than non-disabled ones. We propose a new framework based on the changing relationship between older people and their environment, in which resource linkage in elderly care utilization is emphasized. We conducted a survey with 139 participants (i.e., older people age 60 years or over with different level of disabilities) in three types of neighborhoods in Beijing, China. By conducting a decision tree analysis under the Person-Environment Link (P-E Link) model, we (1) characterized unmet needs for elderly care (activities of daily living (ADL) and instrumental activities of daily living (IADL) assistance) among community-dwelling disabled older people; (2) found disabled older people had more unmet needs for both ADL and IADL assistance because of a lack in linkages to care resources than non-disabled ones; and (3) characterized the linkages to care resources for better supporting disabled older people to age in place, including family support, social connection, and spatial environment. Our findings help improve the Anderson behavioral model by characterizing enabling environments, which highlights that not only the availability of enabling resources but also linkages to these enabling resources play an important role in meeting needs for care among disabled older people. Our findings can also inform improvements in policy design that are targeted to reduce elderly care inequalities.

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Harrison, John. „Health care access and equality for disabled people“. British Journal of Therapy and Rehabilitation 6, Nr. 8 (August 1999): 380–83. http://dx.doi.org/10.12968/bjtr.1999.6.8.13950.

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Court, C. „Community care means extra cost for disabled people“. BMJ 311, Nr. 7005 (02.09.1995): 588. http://dx.doi.org/10.1136/bmj.311.7005.588.

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Dissertationen zum Thema "Care of disabled people"

Scott, Heather J. „The role of housing in community care for mentally disabled people“. Thesis, Durham University, 1992. http://etheses.dur.ac.uk/5732/.

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It is argued that housing is a fundamental element in successful community care programmes for people who have a long-term mental illness, but that the significance of the immediate living environment on the individual's psych- social well-being has been underestimated in the formulation and implementation of policy. Using a grounded theory approach. Part One reports an exploratory study of the catchment area of one psychiatric hospital, which included parts of three health districts and three local authority areas. The study examined in detail, with a focus on housing, the operation of services for mentally disabled people , the plans for creating locally-based facilities, and the implementation of those plans in the mid-1980's, by means of a combination of documentary evidence and key informant interviews. All three parts of the study area were found to have encountered major but differing problems. Wide variations between and within local areas in policy and resources were found, but most stiking was the emergence of two distinct key informant perspectives: those of policy makers/managers, and workers in face-to-face contact with mentally disabled people, indicative of separate discourses of rights and needs. Part Two sets up a model of three functions of housing based on psychological needs, and argues for a compensatory role for housing in community care, which is contrasted with the reality of increasing difficulty in meeting even basic survival needs. It is suggested that the emphasis on negative rights of much mental health reform was inadequate to ensure that needs were met when the welfare net began to contract, and renewed emphasis on citizenship and social rights is proposed as a means to represent more adequately the housing needs of mentally disabled people at the levels of policy and service planning.

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Sullivan, Jacqueline Patricia Clay Tubbs. „Pastoral care to younger adults in long-term care“. Theological Research Exchange Network (TREN), 1997. http://www.tren.com.

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Hulland, Sarah A. „A retrospective review and analysis of the need for a hospital-based dental care program for the adult with disabilities“. Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq28770.pdf.

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Easterling, Calvin Henry. „The Developmentally Disabled Elderly in Canada: Access to Health Care and Social Services“. Thesis, University of North Texas, 1992. https://digital.library.unt.edu/ark:/67531/metadc332746/.

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The accessibility, predictors, and use of health care and social services among developmentally disabled elderly adults in Canada were examined using a nationally representative social survey. The first research hypothesis is that the independent variables will contribute significantly to the prediction of the dependent variables. A second hypothesis is that the slope of any given independent variable will not equal zero. The results of this research show that the illness (need) variables are the most predictive correlate of the utilization of health care and social services. The predisposing variables have secondary explanatory power, with the enabling variables accounting for the least amount of variance. The hypotheses were tested by step-wise multiple regression analysis using SPSS-X.

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Lech, Patricia Griffith. „The Increase in Disabled Workers and Healthcare Provider Incentives“. Fogler Library, University of Maine, 2009. http://www.library.umaine.edu/theses/pdf/LechPG2009.pdf.

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Clear, Mike, of Western Sydney Hawkesbury University und of Health Humanities and Social Ecology Faculty. „Public discourse personal reality: disablement and a re-search for caring culture“. THESIS_FHHS_xxx_Clear_M.xml, 1996. http://handle.uws.edu.au:8081/1959.7/34.

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This thesis explored the lives of carers of disabled people, and the research process itself within the collaborative framework of a support group. It used as its data sources an extensive review of the literature, interview transcripts and fieldnotes from carers, participants from the local service system, and the records of meetings and activities of the Group over 5 years. The study highlights the way public discourse on deinstitutionalisation has so captured our consciousness on care of disabled people that the personal reality of care in the family home has been effectively lost. It traces the disordering discourses of disablement and their link with constructions of caring. The personal reality of care and the isolating nature of this union of caring and disablement was the primary research focus. This may be characterised by social loss, and a lifestyle bound up with disablement which involves a search for a supportive or caring culture. The isolation and exclusion of carers occurs behind the screens of apparently caring institutions such as marriage, family, community and the service system. In the search for a caring cuture carers find their lives bound up with that of state and service systems which offer some hope of a supportive response. Instead they invariably find that the culture is an alien one. The research informed attempts of the Group to explore improved forms of caring culture, and more relevant public policy approaches. The study attempted to bridge the gap between the process of knowledge construction and discourse, and the material experience of carers
Doctor of Philosophy (PhD)

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Kelleher, Anne L. „Caring for disabled husbands : wives' perspectives“. Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/29698.

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There is presently an increasing trend towards deinstitutionalization of several different populations, including physically disabled adults. Although a variety of staffed resources provide for alternative care, 'home' and 'family' remain the primary resource in the community based care system. Given that the family of the 1980's has a decreased capacity to care due to such factors as increased mobility and loss of extended family networks we must be concerned with the continued viability of this resource. And, given that 'family’ is often a euphemism for 'nearest female relative' and that women's role in society has changed markedly in recent years the issue of women as caregivers is one of particularly urgent concern. This study is based on extensive interviews with eight women caring for disabled husbands. The interview schedule and methodology facilitated descriptive data regarding caregiving tasks as well as a comprehensive exploration of what was problematic about the day to day reality of caregiving for these women. The data analysis identified struggling with the 'role' of wife-caregiver, isolation and a changed marital dynamic as primary themes in the process of caregiving. This study provides some insight into what is problematic about caregiving for these wives and some suggestions for improving social work practice and providing more effective services in relation to this population.
Arts, Faculty of
Social Work, School of
Graduate

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Bonnett, David Christopher Sturgess. „The design effectiveness of residential care homes for independent living of young physically disabled people“. Thesis, Oxford Brookes University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.282640.

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Brandon, Toby. „Power and disabled people : a comparative case study of three community care services in London“. Thesis, London School of Economics and Political Science (University of London), 1999. http://etheses.lse.ac.uk/1589/.

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The main research question addressed is how the perceptions and experiences of people with disabilities around what is termed 'quality of life' are enhanced or modified by differing service delivery systems. This approach is based on the assumption that people with disabilities have unique knowledge about services, providing a core understanding of the power around decision making and its effects on their lives. The perspectives and methodology used are underlined by concepts of user autonomy, social control, independence, interdependence, advocacy, respect and citizenship. The case study methodology provides an in-depth focus on both 'positive' and 'negative' ethics in social science. The research area was examined within a multi-professional framework and aimed at a triangulation of perspectives from participant observation, user and professional interviews, tailored vignettes and organisational documentation from services formally designed to empower their users following the latest government policy. The research, following the principles of grounded theory, examined to what extent care management and advocacy, residential support and service brokerage and a more traditional day centre system were achieving these primary aims. The qualitative data generated by the research gives rise to a socio-organisational power analysis of 'service forums'. The service forums are constructed from 'service postures' and 'service cultures'. Service posture refers to the set of formal values and beliefs owned by an organisation. The service posture for the residential consortium is summarised as 'normality', the day centre's as 'respect' and the care management organisation's as 'advocacy'. The organisations' service cultures are the unofficial presentation of the service, shown to come from the service posture, either being complementary, its antitheses, or quite separate. It is clear that the behaviour of the workers and the structure of the three organisations studied have both distinct and profound effects on their users' senses and experiences of power. The conclusion explores the elements of disability, choice and decision making which make up the socio-organisational power structures with respect to each organisation. Finally ways in which a participatory service delivery system could be constructed are considered in the context of training, policy and organisational structure.

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Rolph, Sheena Elizabeth. „The history of community care for people with learning difficulties in Norfolk, 1930-1980“. [n.p.], 1999. http://library7.open.ac.uk/abstracts/page.php?thesisid=83.

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Bücher zum Thema "Care of disabled people"

Glendinning, Caroline. Involving disabled people in community care planning. Manchester: University of Manchester, 1993.

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Independent lives?: Community care and disabled people. Basingstoke: Macmillan, 1993.

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Assessing physically disabled people at home. London: Chapman and Hall, 1990.

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The chronically disabled elderly in society. Westport, Conn: Greenwood Press, 1994.

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Diane, Rowland, und Lyons Barbara 1957-, Hrsg. Financing home care: Improving protection for disabled elderly people. Baltimore: Johns Hopkins University Press, 1991.

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Anna, Briggs, und Oliver Judith, Hrsg. Caring: Experiences of looking after disabled relatives. London: Routledge & K. Paul, 1985.

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Liu, Korbin. Home care expenses for the disabled elderly. [Baltimore, Md.?: Health Care Financing Administration, 1985.

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McCuen, Gary E. Treating the mentally disabled. Hudson WI: McCuen, Gary E., 1988.

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Library of Congress. Congressional Research Service, Hrsg. Medicaid: Eligibility for the aged, disabled, and blind. [Washington, D.C.]: Congressional Research Service, Library of Congress, 1993.

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Atkinson, F. I. Physically disabled people at home: Nursing care and informal carers. Edinburgh: University of Edinburgh, Nursing Research Unit, 1990.

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Buchteile zum Thema "Care of disabled people"

Morris, Jenny. „Disabled people as ‘care-givers’“. In Independent Lives?, 89–101. London: Macmillan Education UK, 1993. http://dx.doi.org/10.1007/978-1-349-23136-2_6.

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Fawcett, Barbara, Brid Featherstone und Jim Goddard. „Disabled Children and Young People“. In Contemporary Child Care Policy and Practice, 114–29. London: Macmillan Education UK, 2004. http://dx.doi.org/10.1007/978-0-230-00623-2_7.

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French, Sally, und John Swain. „Disabled People: Health and Social Care“. In Working with Disabled People in Policy and Practice, 47–58. London: Macmillan Education UK, 2012. http://dx.doi.org/10.1007/978-0-230-58884-4_4.

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French, Sally, und John Swain. „Residential Care“. In Working with Disabled People in Policy and Practice, 59–74. London: Macmillan Education UK, 2012. http://dx.doi.org/10.1007/978-0-230-58884-4_5.

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French, Sally, und John Swain. „Control of Health and Social Care Services by Disabled People“. In Working with Disabled People in Policy and Practice, 75–102. London: Macmillan Education UK, 2012. http://dx.doi.org/10.1007/978-0-230-58884-4_6.

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Kroll, Aleksandra. „Taking care of a severely disabled child at home: Caregivers’ burden and chance of personal growth“. In People, Care and Work in the Home, 140–55. Milton Park, Abingdon, Oxon ; New York, NY : Routledge, 2020. | Series: Routledge advances in sociology: Routledge, 2020. http://dx.doi.org/10.4324/9780367823351-12.

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Kotásková, Pavla, Jitka Fialová, Mariana Jakubisová, Miloslav Šlezingr und Pavlína Procházková. „Possible Use of Water Areas by Disabled People“. In Water Management and the Environment: Case Studies, 3–28. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-79014-5_1.

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Reinhold, Karin, Piia Tint, Ada Traumann, Piret Tamme, Viiu Tuulik und Silja-Riin Voolma. „Digital Support in Logistics of Home-Care Nurses for Disabled and Elderly People“. In Advances in Intelligent Systems and Computing, 563–68. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-25629-6_87.

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Gaiduk, Maksym, Lucas Weber, Ralf Seepold, Natividad Martínez Madrid, Massimo Conti und Simone Orcioni. „Involving the Disabled or People in Long-Term Care in Tourism Activities by the Use of Appropriate Technologies“. In Social Innovation in Long-Term Care Through Digitalization, 87–95. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-16855-0_10.

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Sudmann, Tobba T., Ingebjørg T. Børsheim, Tomasz Ciamulski, Jakub Wagner, Knut Øvsthus und Frode F. Jacobsen. „Ultra-Wide Band Radar Monitoring of Movements in Homes of Elderly and Disabled People: A Health Care Perspective“. In Computer Systems for Healthcare and Medicine, 1–29. New York: River Publishers, 2022. http://dx.doi.org/10.1201/9781003337683-1.

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Konferenzberichte zum Thema "Care of disabled people"

Aloufi, Khalid. „IoT Based Health Care System for Elderly and Disabled People“. In International Conference on Recent Advances in Computer Systems. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/racs-15.2016.15.

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Misbahuddin, Syed, Humam Orabi, Ryan Fatta, Mishary Al-Juhany und Azzam Almatrafi. „IoT Framework Based Health Care System for Elderly and Disabled People“. In International Conference on Recent Advances in Computer Systems. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/racs-15.2016.16.

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Long, Siying, und Jing Yang. „Application of Brain-Computer Interface for Disabled People on Human Factors Engineering“. In 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1001903.

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Brain-Computer Interface (BCI) is a new type of human-computer interaction technology, which has achieved good theoretical results so far, but still faces many problems in the practical application of the technology. At present, the main group of people who use BCI technology is the disabled, because this technology can improve the self-care ability of disabled people, but the application design of traditional brain-computer interface in the past did not start from them well. Based on human factors engineering, this paper will analyze the characteristics of disabled people, combine the existing theoretical characteristics of BCI, optimize the application of BCI, and design unique and intelligent application scenarios for them. This can greatly improve people's awareness and acceptance of BCI technology, and promote the development of BCI technology.Keywords: Human Factor Engineering, Brain-Computer Interface, Disabled People, Intelligent Application

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MacAulay, F. „The development of ICU-Talk a communication aid for patients in intensive care units“. In IEE Seminar on Speech and Language Processing for Disabled and Elderly People. IEE, 2000. http://dx.doi.org/10.1049/ic:20000138.

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Vazquez, L. J. G., M. A. Minor und A. J. H. Sossa. „Low cost human computer interface voluntary eye movement as communication system for disabled people with limited movements“. In 2011 Pan American Health Care Exchanges (PAHCE 2011). IEEE, 2011. http://dx.doi.org/10.1109/pahce.2011.5871871.

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Brito da Silva, Andressa, Gabriela Gonzaga Magalhães da Silva, Caroline de Souza e Silva Guimarães, Carla Aparecida Lourdesdos S. de Azevedo und Patrick Wagner de Azevedo. „Taking care of the caregiver: the meanings unveiled to the caregiver of people with disabilities“. In 7th International Congress on Scientific Knowledge. Perspectivas Online: Humanas e Sociais Aplicadas, 2021. http://dx.doi.org/10.25242/8876113220212450.

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In the act of caring, it was widely disseminated as important lookingat the person being cared for and the needs that could be revealedin the construction of the relationship throughout the care process with the caregiver. In this research, our gaze is directed to the caregiver, making it possible to enablewhich meanings, values and beliefs are presentedin the conduct of their lives and how thedialogue with the current speechesin society try to capture them from modelsthat obscure the production of their subjectivity. In this regard, human relationships can be created and always recreated,and any dogmatic forms of relationship can produce limitations of meaning and existential suffering. As a general objective, we sought to understand the production of subjectivity of the caregiver of people with disabilities in the encounter with the disabled subject to be cared for. As specific objectives, to analyze the meanings that permeate the relationship between the caregiver and the person with a disability, in addition to investigatethe meanings unveiled in work relationships and in the affectiverelationships between the caregiver and the person with a disability. The specific objectives analyze the meanings related to the work relationship and affection that goesthrough the crossingswith a care character. In this way, families received specialattention, as many caregivers are family members, withoutdisregardingthe importance of professionals hired to exercise the role of caregiver. With regard to methodology, the guiding methods of the research were Cartography and Phenomenology, using semi-open interviews, as well as a systematic literature review. Ten interviews were produced frompeople of the professional field tocaregivers whose familymembers demanded care due to being disabled. It was possible to noticeresults about the phenomenonand singularities of the established relationshipsthat care implied in a deep existential investment by all respondents, both those who proposed to be involved by job function and those which life directed them in favor of a family member or close person. The speeches that initially seemed well structured, gradually unveiled meanings that indicated a deep regret for the suffering and the severe condition of limitation of the person to be cared for. The searchingfor meaning went beyond mere rationality, and spirituality became a key element in the attempt to nurture existential anxieties. Several participants emphasized that despite the constant physical fatigue and emotional exhaustion, consideringthe complexity of each case in particular, the satisfaction of being able to help, reciprocate or even be useful by applying care made this relationship lighter and more meaningful. Contradictory feelings such as love and a feeling that the caregiver's life is paralyzed, due to the dedication to the person to becared for, clearly emerged

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Moelmann, Connor, Phillip Davis, Josh Getz, Alex Pham, David Wobith, Albert Shih und Dick Sarns. „A Walker With Integrated Toilet Seat and Stroller Capabilities for the Disabled“. In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14763.

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With the baby boomers reaching retirement, we anticipate a large increase in demand of health care products for the elderly. As people age, bones become fragile and balance becomes impaired, which puts older people at increased danger with longer recovery times. Dick Sarns, the sponsor of this project and co-founder and CEO of NuStep, a rehabilitation equipment manufacturer, wanted to create a walker for his wife, Norma Sarns, who suffers from multiple sclerosis.

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Allagha, Mohammad, Oskar Kruschitz, Katherina Voss, Stefanie Binder und Kevin Truckenthanner. „Digital Matching for live-in care“. In 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002579.

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In Austria, 25,000 to 30,000 people being cared for by live-in caregivers. Live-in caregivers are defined as workers who are employed to provide care services to elderly and disabled people living in their private households. Activities in home care are predominantly carried out by immigrant women because of the special conditions that home care provides. These conditions can have many positive aspects for both the care workers and the care recipients, if they are well and appropriately matched to the skills of the caregivers and the needs of the persons being cared for. The live-in caregivers in Western countries come mostly from Eastern Europe. On the one hand, because of the worldwide shortage of qualified care workers and, on the other hand, due to the higher wages in contrast to their home countries and the prospects that such a position brings with it.However, they can also bear risks of dependency on their employers, leading to isolation, on-call work, and the risk of exploitation, while putting live-in care workers in a particularly vulnerable position with respect to immigration policy. Working conditions are often extremely harsh, with fees and contracts strictly regulated by recruiting agencies.Live-in care workers are an important but forgotten sector of long-term care. Without improving their working conditions, we will not be able to provide affordable, quality care to citizens, who are very urgently in need of this service. Even though this is often the only affordable solution for affected families. In order to improve the working conditions and to ensure that the caregivers continue to be employed in households that best match their skills and aspirations, we have created a new live-in care matching platform. Before creating the platform, we conducted focus group interviews to find out what is important to the stakeholders.Together with families of people in need of care and care workers, we developed a platform that meets the requirements of both sides and optimally supports both sides in the placement process. Here, both caregivers and persons in need of care (or their families) have the opportunity to disclose what they value, what skills they possess and what special features there are by answering a questionnaire. Using an innovative matching algorithm, the platform selects the ideal combination of caregivers and persons in need of care. In this paper, we will analyze the results of the focus group interviews in more detail, elaborate on the lessons learned and discuss which attributes play a particular role in the matching process based on our algorithm. In the future, the process should be simplified for both parties and will serve as a validation for the stakeholders

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Kumar, N. Dinesh, und A. Sushmitha Mala. „Practical Implementation of 3D Smart Walking Stick for Blind People“. In International Conference on Women Researchers in Electronics and Computing. AIJR Publisher, 2021. http://dx.doi.org/10.21467/proceedings.114.51.

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The gift of god that is precious is vision through which, one can see the beautiful world and enjoy. But many people throughout the world are deprived of this According to October 2017 report of World Health Organization (WHO) an estimated 253 million people live with vision impairment. 36 million are blind and 217 million have moderate to severe vision impairment. Un-operated cataract is the main reason for blindness in low income and developing countries Even in China by the end of 2017, the population over 60 will reach 241 million, accounting for 17.3 percent of the country's total population and nearly 40 million are disabled and semi disabled, according to data released by the Committee for the elderly in 201 d. So, in this case most of the visually challenged people cannot afford an expensive device to use as their supporter. So, in this paper we have proposed a cost-effective 3D intelligent Walking device. This mainly depends on the sensors because they can improve the world through diagnostics in many applications and it helps to improve performance. This device is implemented using ARM Controller, IR Sensors, Vibration Sensor, as well as GSM and GPS for location Sharing. Also a voice module is introduced along with this to give the directions through audio format. This Entered device is programmed by simple machine Learning algorithms to optimize the machine.

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Silva, Andressa Brito da, Gabriela Gonzaga Magalhães da Silva, Ingrid de Azevedo Alves, Caroline de Souza e. Silva Guimarães, Carla Aparecida Lourdes dos Santos de Azevedo und Patrick Wagner de Azevedo. „In the encounter with variance: a study about the production of subjectivity of the caregiver of disabled people and the resulting implication in the care addressed to the people with disabilities“. In V Seminário de Pesquisa e Desenvolvimento PROVIC/PIBIC - II Encontro de Iniciação Científica CNPq. Perspectivas Online: Humanas e Sociais Aplicadas, 2020. http://dx.doi.org/10.25242/8876102820202198.

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Berichte der Organisationen zum Thema "Care of disabled people"

Pezzin, Liliana, Robert Pollak und Barbara Schone. Long-Term Care of the Disabled Elderly: Do Children Increase Caregiving by Spouses? Cambridge, MA: National Bureau of Economic Research, September 2008. http://dx.doi.org/10.3386/w14328.

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Garber, Alan. Long-Term Care, Wealth, and Health of the Disabled Elderly Living in the Community. Cambridge, MA: National Bureau of Economic Research, Juli 1987. http://dx.doi.org/10.3386/w2328.

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Tranby, Eric P., Yara A. Halasa-Rappel, Avery R. Brow, Matt Jacob und Julie Frantsve-Hawley. The Burden of Out-of-Pocket Expenditures for Dental Care on Medicare-enrolled Elderly and Disabled. DentaQuest Partnership for Oral Health Advancement, Februar 2020. http://dx.doi.org/10.35565/dqp.2020.2002.

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Esu-Williams, Eka, Katie Schenk, Joseph Motsepe, Scott Geibel und Anderson Zulu. Involving young people in the care and support of people living with HIV/AIDS in Zambia. Population Council, 2004. http://dx.doi.org/10.31899/hiv2.1037.

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Butler, Mary, Joseph E. Gaugler, Kristine M. C. Talley, Hamdi I. Abdi, Priyanka J. Desai, Susan Duval, Mary L. Forte et al. Care Interventions for People Living With Dementia and Their Caregivers. Agency for Healthcare Research and Quality (AHRQ), Juli 2020. http://dx.doi.org/10.23970/ahrqepccer231.

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Ciapponi, Agustín. Do community health workers improve the care of people with hypertension? SUPPORT, 2016. http://dx.doi.org/10.30846/161007.

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Community health workers (CHWs), carry out functions related to healthcare delivery, have no formal professional designation to deliver healthcare, but are trained as part of an intervention, and have a relationship with the community being served. They can be used to facilitate improvement in the management of chronic conditions like hypertension.

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Ciapponi, Agustín. Do community health workers improve the care of people with hypertension? SUPPORT, 2016. http://dx.doi.org/10.30846/160807.

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Moore, Tim, Morag McArthur, Steven Roche, Jodi Death und Clare Tilbury. Safe and Sound: Exploring the safety of young people in residential care. Australian Catholic University, Januar 2016. http://dx.doi.org/10.24268/fhs.8140.

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Esu-Williams, Eka, Catherine Searle und Anderson Zulu. Involving young people in the care and support of people living with HIV in Zambia: An evaluation of program sustainability. Population Council, 2008. http://dx.doi.org/10.31899/hiv12.1005.

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Ciapponi, Agustín, und Sebastián García Martí. Does home-based care reduce morbidity and mortality in people living with HIV-AIDS? SUPPORT, 2016. http://dx.doi.org/10.30846/160416.

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