Littérature scientifique sur le sujet « Quality of social care »

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Articles de revues sur le sujet "Quality of social care"

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Bower, B. « Quality Day-Care and Social Growth ». Science News 132, no 4 (25 juillet 1987) : 54. http://dx.doi.org/10.2307/3971995.

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Dutrénit, Jean-Marc. « Evaluation of Quality in Social Care ». Evaluation Review 29, no 5 (octobre 2005) : 441–53. http://dx.doi.org/10.1177/0193841x05278613.

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Hurst, Keith. « SPECIFYING QUALITY IN HEALTH AND SOCIAL CARE ». International Journal for Quality in Health Care 4, no 3 (1992) : 193–97. http://dx.doi.org/10.1093/oxfordjournals.intqhc.a036719.

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Proctor, E. K. « Quality of care and social work research ». Social Work Research 26, no 4 (1 décembre 2002) : 195–97. http://dx.doi.org/10.1093/swr/26.4.195.

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Phillips, Deborah, Kathleen McCartney et Sandra Scarr. « Child-care quality and children's social development. » Developmental Psychology 23, no 4 (1987) : 537–43. http://dx.doi.org/10.1037/0012-1649.23.4.537.

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Weaver, Jenny. « Book Review : Quality Counts. Achieving Quality in Social Care Services ». British Journal of Occupational Therapy 56, no 7 (juillet 1993) : 264. http://dx.doi.org/10.1177/030802269305600717.

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Greenblatt, Fred S. « From Custodial Care to Quality Care ». Loss, Grief & ; Care 6, no 4 (14 mai 1993) : 87–98. http://dx.doi.org/10.1300/j132v06n04_12.

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Stephenson, Jo. « Large social care providers ». Children and Young People Now 2021, no 10 (2 octobre 2021) : 38–39. http://dx.doi.org/10.12968/cypn.2021.10.38.

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Large private companies continue to play an increasing role in the provision of children's home and fostering placements. Jo Stephenson analyses what the data says about the quality of large providers
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Dunkerley, Bill. « The Care Quality Commission in a post-pandemic social care sector ». Nursing and Residential Care 23, no 11 (2 novembre 2021) : 1–2. http://dx.doi.org/10.12968/nrec.2021.23.11.5.

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Kendall-Raynor, Petra. « Social care staff maintaining quality in ‘toughest climate’ ». Nursing Older People 29, no 9 (31 octobre 2017) : 8–9. http://dx.doi.org/10.7748/nop.29.9.8.s8.

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Thèses sur le sujet "Quality of social care"

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Momanyi, Kevin. « Enhancing quality in social care through economic analysis ». Thesis, University of Aberdeen, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=240815.

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Population ageing has motivated policy makers around the world to focus on how best to organise health and social care services to meet an aniticipated growing demand on services. Two popular initiatives are reablement and telecare. Reablement is an approach within homecare that enables older individuals with social care needs to improve their functional performance and live independently. Telecare, on the other hand, involves use of devices to monitor individuals' health and safety, and provide response when needed. This thesis investigates the effectiveness of reablement and telecare by conducting a comprehensive review of the literature and undertaking three empirical studies. It is composed of six chapters. The first chapter presents a theoretical model that links the demand for reablement and telecare to various outcomes. The model is estimated using a strategy that controls for the effects of confounding variables and unobservable factors, and is general in the sense that it nests several other estimation strategies and study designs as special cases. The next chapter contains the literature review. Chapters 3, 4 and 5 present the three empirical studies. The first study investigates the effect of telecare on independent living at home; the second study determines the relationship between the use of telecare and admission to hospital, while the third study determines the relationship between telecare use and the length of stay in hospital. Chapter 6 concludes the thesis and provides some suggestions for further research. Unlike the results of the previous studies, the findings from this thesis suggest that the treatment effects are not homogenous across the poulation and also vary depending on the type of telecare device under consideration.
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Kocman, David. « Quality matters : re-formatting the boundaries of care in Czech social care policy ». Thesis, University of Kent, 2013. https://kar.kent.ac.uk/47654/.

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This thesis deals with knowledge about the mechanics and effects of quality reforms in public service as advanced by critical policy studies. Critical policy studies have identified managerialism and marketization of public services as key conditions in introducing quality reforms. The argument has been built in opposition to proponents of quality who argue that marketization, when introduced to services, enhances their quality. In contrast, critical studies have shown that quality reforms have restructured organizational contexts of public services where quality acted mainly as a rhetorical figure, and where improvements remain dubious. The real effects of quality reforms, they argue, are increased control over practitioners’ labour process and de-professionalization. This thesis is a case study of a recent Czech social care reform. The Czech case is a case of a quality reform without marketization and managerialism, yet with a similar outcome in the form of managerialised care. As such, the Czech case offers an opportunity to further our knowledge about the mechanics of quality reforms provided we make a methodological step outside the analytics of managerialism. The thesis undertakes this methodological shift by drawing on Actor Network Theory. The question this thesis asks is how could managerialised care be achieved without either marketization or managerialism? Methodologically, the thesis argues that mapping social alliances among policy actors is necessary but in itself not sufficient to explain the outcome. The thesis traces the Czech quality reform from its inception as a policy project at the Ministry of Labour and Social Affairs to its circulation in social care sector. The Czech case shows how articulating quality service in quality standards re-organised care by extending (both conceptually and practically) its boundaries. Care traditionally understood as interactional bodywork was extended horizontally to include practices and forms outside the practitioner-client interaction (such as support planning), and it was extended vertically shifting the agency in care from an equipped practitioner to an equipped service. The contribution of the thesis is twofold. It shows that quality has gained a life in its own outside the managerialist causation model and may not necessarily follow in the footsteps of marketization and managerialism. Mainly, the thesis shows that quality is a complex shibboleth able to re-format the content of practitioner work rather than merely re-structure organizational contexts of public service provision.
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English, Christine. « Judging quality : parents' perspectives of the quality of their child's hospital care ». Thesis, Northumbria University, 2017. http://nrl.northumbria.ac.uk/31608/.

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Background - UK healthcare has adopted various improvement strategies from business including using satisfaction surveys. However, the way patients form and express judgements of quality care can be more complex than customer purchases. Research in adult patient satisfaction has found capturing patient opinion challenging; however, adult service- user views continue to underpin quality care guidance across healthcare. Development of knowledge to include parental views of quality care is important to inform future guidance specific to children’s services. Methods - This study aimed to examine how parents determined the quality of care provided when their child was hospitalised, factors influencing perceptions of care and whether these judgements changed over time. Using a grounded theory approach, data were collected through a series of in-depth interviews (22) with nine parents following their child’s hospitalisation. Findings - The substantive grounded theory - Parenting in an alien hospital world: on guard and on behalf offers new perspectives on the complex psychosocial processes underlying parents’ quality judgements. When their child was hospitalised parents landed in an ‘alien’ world but continued to try 'to parent' (protect and advocate) their child. Parents' experiences were characterised by landing; moving from being' new parents' to 'old hands'; searching for and judging the 'clues' and facing dilemmas of how best to respond to professionals. Parents were found to use an escalating level of signals to prompt health professionals to respond to their queries and concerns Parents' personal lens altered through their transitional journey and this, together with their perception of professionals' power impacted on their chosen responses to professionals and their quality judgements. Parents held two views of care quality: ‘at the time’ and a final ‘on balance’ view. The final view recognised their own heightened emotions and reflected their current transition. Conclusions - Ultimately parents judge hospital care as high quality when they perceived health professionals acted as their allies in their parenting roles as protectors and advocates for their child in the alien hospital world. Health professionals could improve parents' experiences and quality judgements of care by early recognition and response to their 'signalling' and by explicitly acting as parental allies.
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Rapley, Mark Timothy John. « Quality of life : a critical approach ». Thesis, Lancaster University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337125.

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Schultz, Rebecka A. « Staff Perceptions of Quality Interactions in Dementia Care ». DigitalCommons@USU, 2019. https://digitalcommons.usu.edu/etd/7629.

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The national aging trend suggests that population of those aged 65 and older will reach 83.7 million by the year 2050. With increasing age comes the growing possibility of one getting some form of dementia. The Alzheimer’s Association expects the number of American’s with dementia to triple from the reported 5 million cases in 2014 by 2050. With a rise in this cognitively impaired population there is reason to look closely at the needs of persons with dementia living in residential facilities and whether or not they are being met. The main focus of residential facilities is to provide aid with physical needs. However, research shows that all people also have social and psychological needs that need to be met to have the highest quality of life possible. Other research shows that residents with dementia spend a majority of their days with little to no social interactions. This study aims to uncover what verbal and nonverbal behaviors, if any, Certified Nursing Assistants (CNAs) in residential care facilities find to be important when interacting with persons with dementia. This study includes the analysis of 11 interviews of CNAs from local facilities and home health companies. Analysis of their responses uncovered very few observable verbal and nonverbal behaviors were actually discussed. What was more apparent was that attitudes and internal behaviors participants considered important drove the use of good verbal and nonverbal communication. Five themes were uncovered. They were: Observable Verbal and Nonverbal Behaviors, Valuing Personhood, Get on Their [Cognitive and Reality] Level, Be a Friend, and Compassion. Excerpts from the interviews are included for examples of how these themes presented themselves.
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Aldousari, Abdulrahman. « Influence of national culture on the social construction of health care quality ». Thesis, University of Surrey, 2015. http://epubs.surrey.ac.uk/807220/.

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The purpose of this study is to examine how national culture influences the social constructions of health care quality in the Kuwaiti primary care. Kuwait has a well- developed primary care system, offering a wide range of services in practices distributed throughout the nation, throughout the day, and on a walk-in basis. Despite its extended hours, relative comprehensiveness and affordability, the primary care service in Kuwait appears to be poorly received by the public. This study employed a qualitative research methodology to investigate how the elements of the Kuwaiti national culture shape the social constructions of health care quality. The study proposal was reviewed by the research ethics committees of the University of Surrey and KIMS, and a favourable ethical opinion was obtained. Participant information sheet were given to potential participants and consent obtained before data collection. Semi-structured interviews were conducted with 42 participants from various stakeholder groups. Data analysis identified three themes that represent the experiences of the various stakeholders’ relating to their social constructions of health care quality in primary care: (1) meanings of health, (2) attitudes towards primary care service, and (3) access to primary care. Within the identified themes, a number of sub-themes were identified, including: (a) the meaning of health, (b) responsibility for one’s health, (c) tensions in doctor-patient communication, (d) doctors feeling ‘undervalued’, (e) gender issues, (f) cultural suitability of primary care, (g) primary care work environment, (h) disproportionate distribution, (i) waiting times, and (j) institutional discrimination. The study found that the high-power distance element of national culture impacts the social constructions of health care quality. Perceptions of power differentials across social groups seem to contribute considerably to the social construction of health care quality. The contribution of this study is towards the body of knowledge on the cultural competence of health care provision in high-power distance cultures.
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Ekström, Anette. « Amning och vårdkvalitet = Breastfeeding and quality of care / ». Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-240-3/.

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Putnam, Robin Irene Abell Ellen Elizabeth. « Social support and the quality of child care practices among participants in the Family Child Care Partnerships program ». Auburn, Ala., 2006. http://repo.lib.auburn.edu/2006%20Fall/Theses/PUTNAM_ROBIN_48.pdf.

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Rababa, Majdi Mohammad. « SOCIAL SUPPORT, RELATIONSHIP QUALITY, AND SELF-CARE BEHAVIORS IN PATIENTS WITH HEART FAILURE ». UKnowledge, 2018. https://uknowledge.uky.edu/nursing_etds/40.

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The purpose of this dissertation was to examine the associations among social support, gender, relationship quality, and self-care behaviors in patients with heart failure (HF). Specific aims were to: 1) compare the psychometric properties of the 12-item and the 9-item European Heart Failure Self-Care Behavior Scale (EHFScBS) when used to measure self-care behaviors in patients with HF in the United States; 2) determine whether gender moderated the association between perceived social support and daily sodium intake in patients with HF; and 3) determine whether a patient’s gender and relationship with the primary family caregiver (spousal or non-spousal) moderated the association between relationship quality and HF self-care. For the first specific aim, reliability and validity of the 12-item and the 9-item EHFScBS were compared by measures of internal consistency of reliability, item analysis, exploratory factor analysis, and hypothesis testing. The 12-item and the 9-item EHFScBS were valid and reliable when used to measure self-care behaviors in the United States. The 9-item EHFScBS was more homogenous with dimensions closer to the originally proposed dimensions when compared to the 12-item EHFScBS. The second specific aim was addressed by secondary analysis of data from The RICH Heart Program HF Registry. A hierarchical multiple regression model was used to determine whether gender moderated the association between social support and daily sodium intake. In our study, gender did not moderate the association between social support and daily sodium intake. The third specific aim was addressed using hierarchical multiple regression analyses to determine whether gender or relationship type moderated the association between relationship quality and HF self-care. Baseline data from an ongoing longitudinal, randomized controlled trial of a patient-caregiver dyadic intervention program were used in the analysis. Relationship quality was measured using the patient version of the Dyadic Relationship Scale, which consists of two subscales: positive dyadic interaction and negative dyadic strain. Heart failure self-care was measured using the 9-item EHFScBS. Positive dyadic interaction was associated with better HF self-care in female patients or patients with a non-spousal relationship with their family caregiver. This dissertation has fulfilled important gaps in the evidence base for the self-care of patients with HF. The findings from this dissertation provided evidence for the validity and reliability of the 9-item EHFScBS when used to measure HF self-care behaviors. It also provided recommendations for future research to measure directed social support to adopt a specific behavior, such as eating low sodium diet, instead of measuring the social support in general. It also emphasized the importance of examining the quality of the relationship between patients and their family caregivers. The findings also pointed to the need for interventions targeting the relationship quality to be tailored according to the patients’ gender or their relationship type with their family caregiver (spousal or non-spousal). A better understanding of how social factors can impact self-care behaviors in patients with HF is essential, as it gives researchers and healthcare providers the prospect of developing effective interventions to improve HF self-care.
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Lam, Yue-ban. « Pastoral care as a process indicator of quality schools ». Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B21304816.

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Livres sur le sujet "Quality of social care"

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Bridget, Warr, Kelly Des et Social Care Association, dir. Quality counts : Achieving quality in social care services. London : Whiting & Birch, 1992.

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Great Britain. Department of Health. A quality strategy for social care. London : Department of Health, 2000.

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Great Britain. Department of Health., dir. A Quality strategy for social care. London : Department of Health, 2000.

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Anne, Connor, et Black Stewart, dir. Performance review and quality in social care. London : Jessica Kingsley Publishers, 1994.

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Ray, Pawson, et Social Care Institute for Excellence., dir. Types and quality of knowledge in social care. London : Social Care Institute for Excellence, 2003.

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Altnagelvin Hospitals Health and Social Services Trust. Altnagelvin Area Hospital. Delivering quality, a clinical & social care governance strategy. [Londonderry] : The Trust, 2002.

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Social Care Institute for Excellence (Great Britain), dir. Types and quality of knowledge in social care. London : Social Care Institute for Excellence, 2003.

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Managing quality in health care. Jaipur : Rawat Publications, 2010.

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Cassam, Emlyn. Quality assurance for social care agencies : A practical guide. Harlow, Essex : Longman Group, 1992.

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Himu, Gupta, dir. Quality Assurance for Social Care Agencies : A Practical Guide. London : Taylor and Francis, 2016.

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Chapitres de livres sur le sujet "Quality of social care"

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Laing, Barbara. « Social workers ». Dans Quality care for elderly people, 189–97. Boston, MA : Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-3003-3_13.

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Law, Vincent Tin Sing. « Social Enterprises in Elderly Care ». Dans Quality of Life in Asia, 361–75. Singapore : Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3061-4_25.

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Maniar, Neil, Tracy Wiedt et Richard Wender. « Understanding the Social Determinants of Cancer : Challenges, Opportunities, and Pathways to Success ». Dans Quality Cancer Care, 37–60. Cham : Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78649-0_4.

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Adams, Robert. « Enhancing Quality 1 : Professional Audit and Progressive Practice in Child Care ». Dans Quality Social Work, 142–70. London : Macmillan Education UK, 1998. http://dx.doi.org/10.1007/978-1-349-13733-6_7.

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Adams, Robert. « Enhancing Quality 2 : Monitoring and Evaluating for Quality in Community Care ». Dans Quality Social Work, 171–99. London : Macmillan Education UK, 1998. http://dx.doi.org/10.1007/978-1-349-13733-6_8.

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Helmes, Edward, et Lynne Austin. « Quality of Life in Residential Care ». Dans Social Indicators Research Series, 105–28. Dordrecht : Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0271-4_7.

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Adams, Robert. « Quality Assurance of Practice ». Dans Foundations of Health and Social Care, 333–41. London : Macmillan Education UK, 2007. http://dx.doi.org/10.1007/978-0-230-22933-4_36.

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Rhodes, Karin Verlaine, et Margaret E. Samuels-Kalow. « Access to Care : Access Is a Prerequisite to Quality ». Dans Social Emergency Medicine, 127–41. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-65672-0_8.

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Izu, Regina Moromizato. « Quality and Equity in Early Childhood Care in Peru ». Dans Education and Social Justice, 175–89. Dordrecht : Springer Netherlands, 2006. http://dx.doi.org/10.1007/1-4020-4722-3_10.

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Vaarama, Marja, Richard Pieper et Andrew Sixsmith. « Care-related Quality of Life : Conceptual and Empirical Exploration ». Dans Social Indicators Research Series, 215–32. Dordrecht : Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-5682-6_13.

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Actes de conférences sur le sujet "Quality of social care"

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Mehdi, Zafar. « Care Workers and Quality of Care in Nursing Homes in Canada ». Dans 5th International Conference on New Findings On Humanities and Social Sciences. Acavent, 2020. http://dx.doi.org/10.33422/5th.hsconf.2020.11.105.

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Grinberga-Zalite, Gunta. « REENGINEERING QUALITY OF PHARMACEUTICAL CARE SERVICES : THE CASE STUDY OF LATVIA ». Dans 4th International Multidisciplinary Scientific Conference on Social Sciences and Arts SGEM2017. Stef92 Technology, 2017. http://dx.doi.org/10.5593/sgemsocial2017/hb31/s13.069.

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Bonsmith, Kathleen, Arti D. Desai, Chuan Zhou, Chen Kenyon, David P. Johnson, Michelle Lopez, Amy Tyler, Sanyukta Desai et Rita Mangione-Smith. « Markers of Social Disadvantage and Hospital Quality of Care for Pediatric Respiratory Illness ». Dans AAP National Conference & Exhibition Meeting Abstracts. American Academy of Pediatrics, 2021. http://dx.doi.org/10.1542/peds.147.3_meetingabstract.592.

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« The Impact of Community Care Service System on the Quality Life of the Elderly ». Dans 2018 2nd International Conference on Social Sciences, Arts and Humanities. Francis Academic Press, 2018. http://dx.doi.org/10.25236/ssah.2018.213.

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Heikkinen, Katja, Mari Lahti, Johanna Berg, Arina Kiseleva et Sini Eloranta. « European Integrated Care Horizon 2020 : increase societal participation ; reduce care demands and costs in Finnish context ». Dans CARPE Conference 2019 : Horizon Europe and beyond. Valencia : Universitat Politècnica València, 2019. http://dx.doi.org/10.4995/carpe2019.2019.10208.

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This project is part of larger European level integrated care project led by HU University of Applied Sciences.Background: In Finland, the integration of social and health care services has taken centre stage in both the policy and practice arenas. The needs of many client groups, for example mental health client, older people and families of child, are many and varied.For example, poor mental health considerably impairs well-being of the population and has considerable economic consequences like absence from work, early retirement and productive losses. Efforts to move towards integrated care in social and health care have been met with increased interest and enthusiasm in recent years. This will increase the focus to improve care and population health while containing costs. However, there is a need to better understand different integrated care approaches for social and health care and guide future implementation of new integrated care models.It is now important to move towards integrated care for many client groups e.g. mental disorders. In this, professionals with different training backgrounds co-ordinate their expertise in providing care for theirshared clients. It provides a safe nexus for the exchange of knowledge and opinions, as well as a framework for reaching a consensus about appropriate health care delivery for a particular client or client cohort. The client should have an immediate access to integrated care, with a focus on rehabilitation in patient’s social roles.Aim: Support societal participation, quality of live and reduce care demand and costs in social and health care client, for example mental health client through integration of healthcare and welfare services.
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Khosla, Rajiv, Mei-Tai Chu, Reza Kachouie, Keiji Yamada, Fujita Yoshihiro et Tomoharu Yamaguchi. « Interactive multimodal social robot for improving quality of care of elderly in Australian nursing homes ». Dans the 20th ACM international conference. New York, New York, USA : ACM Press, 2012. http://dx.doi.org/10.1145/2393347.2396411.

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Nossiter, J., M. Morris, M. Parry, A. Sujenthiran, A. Aggarwal, P. Cathcart, H. Payne, N. Clarke et J. van der Meulen. « P11 Improving prostate cancer care through the ‘outlier process’ : a national quality improvement workshop ». Dans Society for Social Medicine and Population Health Annual Scientific Meeting 2020, Hosted online by the Society for Social Medicine & Population Health and University of Cambridge Public Health, 9–11 September 2020. BMJ Publishing Group Ltd, 2020. http://dx.doi.org/10.1136/jech-2020-ssmabstracts.107.

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Arbour, MaryCatherine, Baraka Floyd, Samantha Morton, Sidney Atwood, Stephanie Doyle, Patsy Hampton et Robert Sege. « 20 Linking pediatric primary care and systems : DULCE expansion via quality improvement advances patient-centered care and addresses health-related social needs ». Dans IHI Scientific Symposium, Gaylord Palms Resort & Convention Center Orlando, Florida, 9th December 2019. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjoq-2019-ihi.20.

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Smolkova, Eva. « FACTORS OF INFLUENCE HEALTH CARE ON THE QUALITY OF LIFE OF THE CITIZENS OF THE SLOVAKIA ». Dans 4th International Multidisciplinary Scientific Conference on Social Sciences and Arts SGEM2017. Stef92 Technology, 2017. http://dx.doi.org/10.5593/sgemsocial2017/hb21/s06.031.

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Harfika, Meiana, Lela Nurlela et Mahesta Ratna Dewi. « The Corellation of Social Environment and Quality of Life People Living At Coastal Areas In Surabaya ». Dans The 9th International Nursing Conference : Nurses at The Forefront Transforming Care, Science and Research. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0008328705670570.

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Rapports d'organisations sur le sujet "Quality of social care"

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Kenny, Caroline, et Robert Wilson. Robotics in Social Care. Parliamentary Office of Science and Technology, décembre 2018. http://dx.doi.org/10.58248/pn591.

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This POSTnote introduces robotic technology and the main ways it has been developed for use in social care. It reviews evidence on the impact of robotics on the costs and quality of social care and its workforce, and explores the main ethical, social and regulatory challenges to its use in social care.
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Zimmerman, Emily, et Jana Smith. Behavioral tactics to support providers in offering quality care : Insights from provider behavior change research and practice. Population Council, 2022. http://dx.doi.org/10.31899/sbsr2022.1043.

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This document offers a synthesis of insights from recent research and design activities conducted by ideas42 through Breakthrough RESEARCH, Breakthrough ACTION, and other projects across nine different low- and middle-income settings about the behavioral roots of challenges health care providers face in providing high quality services. We discuss how the physical and social environment in which they work and live sends signals to providers about what is important, how they can navigate difficulties, and how well they are performing. We discuss how experiences outside the health facility impact how providers approach their professional duties. We also discuss how pervasive time and resource constraints create a cognitive and emotional burden that gets in the way of what they can do, even within these constraints. For each challenge, we also share lessons emerging from this research about about how global health practitioners can address these challenges through program design and implementation.
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Opiyo, Newton. What are the effects of interprofessional education on professional practice and healthcare outcomes ? SUPPORT, 2017. http://dx.doi.org/10.30846/170413.

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Delivering effective, high quality patient care is complex and requires that health and social care professionals work together effectively. Interprofessional education – training or learning initiatives that involve more than one profession in joint, interactive learning with the explicit purpose of improving interprofessional collaboration or patient care – is a possible strategy for improving how professionals work together as well as improving professional practice and patient care.
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Anderson, Kristy A., Anne M. Roux, Hillary Steinberg, Tamara Garfield, Jessica E. Rast, Paul T. Shattuck et Lindsay L. Shea. The Intersection of National Autism Indicators Report : Autism, Health, Poverty and Racial Inequity. A.J. Drexel Autism Institute, avril 2022. http://dx.doi.org/10.17918/nairintersection2022.

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This report examines the following two questions: 1) do income-based differences in health and health care outcomes look the same for children with and without autism? and 2) do income-based differences in health and health care outcomes look the same for BIPOC (Black, Indigenous, and People of Color) children with autism and white children with autism? Examining the health and healthcare outcomes of children with autism in combination with other social characteristics offers several advantages. First, we can illuminate how demographics alone, and in combination with other social characteristics of children, are associated with differences in the rates of health and healthcare outcomes they experience. Second, it increases our understanding of the health-related experiences of social groups who are often neglected in research. Third, it provides current and comprehensive evidence on how children with autism experience relative disadvantages related to social determinants of health, which are aspects of the environment that affect health, functioning, and quality-of-life outcomes and risks.
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FEDOTKINA, S. A., O. V. MUZALEVA et E. V. KHUGAEVA. RETROSPECTIVE ANALYSIS OF THE USE OF TELEMEDICINE TECHNOLOGIES FOR THE PREVENTION, DIAGNOSIS AND TREATMENT OF HYPERTENSION. Science and Innovation Center Publishing House, 2021. http://dx.doi.org/10.12731/978-0-615-67320-2-4-22.

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Introduction. The economic losses associated with disability due to diseases of the circulatory system, as well as the costs of providing medical care to patients suffering from heart and vascular diseases, are increasing annually. The state preventive measures currently being carried out are of a delayed nature. The results of the medical examination of the population of the Russian Federation in recent years (2015-2019) indicate that the incidence of cardiovascular diseases, including hypertension, is at a fairly high level. In the middle of the last century, the Concept of risk factors for the development of chronic non-communicable diseases were formulated, in the structure of which cardiovascular diseases, including arterial hypertension, occupies one of the primary positions. The concept is based on the results of promising epidemiological studies, and, at present, is a methodological basis for planning and organizing primary prevention of cardiovascular diseases. The purpose of the study. Based on the analysis of literary sources (including foreign ones) containing experience in the use of telemedicine technologies, to assess their significance for the prevention, diagnosis and treatment of hypertension, as well as forecasting improvements in the quality of medical care when adapting to the use of clinical recommendations. Materials and methods. The article provides an analytical review of the use of modern telemedicine technologies in the prevention of hypertension. The results of the study and their discussion. The analysis of literary sources has shown that in the context of the progress of information and telecommunication technologies in the healthcare system, a fundamentally new direction has appeared in the organization and provision of medical care to the population - telemedicine, which will ensure the modern level of prevention, detection and treatment of chronic non-communicable diseases, and also determines positive medical, social and economic performance indicators. To date, updates in the legislative framework of the Russian Federation are aimed at ensuring that medical care with the use of telemedicine technologies is more widespread, taking into account the standards of medical care and clinical recommendations. Conclusion. Based on a review of literature sources, it has been established that the modern solution to the problem of improving the quality of medical care for patients, including those with hypertension, diseases is medical care using telemedicine technologies that prove their medical, social and economic effectiveness.
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Bocioaga, Andreea. Health and Social Care Systems Redesign. Iriss, octobre 2020. http://dx.doi.org/10.31583/esss.20201009.

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Cedergren, Elin, Diana Huynh, Michael Kull, John Moodie, Hjördís Rut Sigurjónsdóttir et Mari Wøien Meijer. Public service delivery in the Nordic Region : An exercise in collaborative governance. Nordregio, février 2021. http://dx.doi.org/10.6027/r2021:4.1403-2503.

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Nordic welfare states are world renowned for providing high quality public services. Nordic municipal and regional authorities, in particular, play a central role in the delivery of key public services in areas, such as, health, education, and social care. However, in recent years, public authorities have faced several challenges which have reduced capacity and resources, including long periods of austerity following the 2008 financial crash, rapid demographic changes caused by an ageing population, and the COVID-19 health crisis. In response to these challenges many public authorities have looked to inter-regional, inter-municipal and cross-border collaborations to improve the quality and effectiveness of public service delivery (OECD 2017; ESPON 2019). Indeed, collaborative public service delivery is becoming increasingly prominent in the Nordic Region due to a highly decentralized systems of governance (Nordregio 20015; Eythorsson 2018).
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Rau, Stefan. Bridge to Future Livable Cities and City Clusters in the People’s Republic of China : Policy Opportunities for High-Quality Urban Development. Asian Development Bank, novembre 2021. http://dx.doi.org/10.22617/wps210372-2.

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The achievements in rapid urbanization and industrialization of the People’s Republic of China (PRC) over the past 40 years were historic. But they came at high environmental and social costs. By 2050, the country will be a high-income, four-generation urban society. Yet, according to the United Nations, the PRC’s population will have halved by 2100. Many cities will lose population and businesses. This will be equally historic and requires urgent action. The author recommends focusing on urban rehabilitation and retrofitting to make cities more livable—with a green circular zero-waste economy, aiming at low-carbon, climate-resilient cities—and making cities healthy and friendly for people of all ages.
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Belais, Albert. Danish day care as a social institution. Portland State University Library, janvier 2000. http://dx.doi.org/10.15760/etd.1999.

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Rocks, Stephen, Giulia Boccarini, Anita Charlesworth, Omar Idriss, Ruth McConkey et Laurie Rachet-Jacquet. Health and social care funding projections 2021. The Health Foundation, septembre 2021. http://dx.doi.org/10.37829/hf-2021-rc18.

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