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Littérature scientifique sur le sujet « Partnership of care givers/family »

Auteur : Grafiati

Publié le 5 avril 2025

Mis à jour le 31 juillet 2025

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Articles de revues sur le sujet "Partnership of care givers/family"

Afzal Javed. "Developing partnership with patients and carers: A need of the time for mental health service delivery." Journal of the Pakistan Medical Association 74, no. 7 (2024): 1217–18. http://dx.doi.org/10.47391/jpma.24-51.

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Contemporary practice of psychiatry is witnessing a radicle shift in the care of mentally ill. As compared to the 20th century, we are now moving towards community psychiatry and large mental hospitals and asylums are closing with a shift to manage these patients closer to their homes. Following these changes in mental health care, current literature provides growing evidence for developing partnership with patients, carers and family members in the delivery of mental health services. While this approach is appreciated for improving the quality of life of patients, there has also been some con

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Sloan, Danetta, Valerie Cotter, Quincy Samus, et al. "My Faith Gives Me Strength: Black Churches Supporting Dementia Care Partners." Innovation in Aging 5, Supplement_1 (2021): 516. http://dx.doi.org/10.1093/geroni/igab046.1995.

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Abstract Inequities in dementia care require an in depth understanding of dementia care partner life experiences, care needs, sources of support and ways to improve those experiences at the community level. In partnership with Black Churches in Baltimore, MD and rural Pennsylvania, we facilitated three focus groups (n=30) with Black dementia care partners to understand: 1) unique dementia care-related needs and challenges, and 2) how the church can be a supportive care partner. Participants noted three overarching themes related to challenges and needs: 1) unique challenges in caregiving - ass

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Basukala, Sulochana. "Care giver burden among spouse of psychiatric patients attending psychiatry outpatient department of a teaching hospital." Journal of Patan Academy of Health Sciences 6, no. 1 (2019): 72–77. http://dx.doi.org/10.3126/jpahs.v6i1.27084.

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Introductions: Caregiver burden in mental illness is a global issue. Burden is more significant and high among spouse than other caregivers. Spouse face illness-specific burdens of feeling powerlessness, fear, marital stress and partnership and family roles. Methods: A cross-sectional study was conducted in outpatient department of psychiatry in Patan hospital, Patan Academy of Health Sciences, Nepal, from 26th August to 23rd September, 2018. Non-probability purposive sampling technique was used. Data was collected from spouses of psychiatric patients by face-to-face interview using Burd

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Maffoni, Marina, Francesco Zanatta, Ilaria Setti, Ines Giorgi, Laura Velutti, and Anna Giardini. "SMiLE to Life: Meaning in life in healthcare professionals working in palliative care and rehabilitation medicine: SMiLE to Life: Meaning in life in healthcare professionals." La Medicina del Lavoro 112, no. 5 (2021): 387–400. https://doi.org/10.23749/mdl.v112i5.11408.

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Background: In the healthcare landscape, various protective factors are identified, such as meaning in life (MiL), namely what gives sense to life events. However, little is known about this construct in the healthcare population. Objectives: To describe MiL among healthcare professionals employed in palliative care and neuro-rehabilitation medicine, unveiling possible differences related to medical specialty and socio-demographic characteristics. Methods: In this cross-sectional and multicentre study, palliative care and neuro-rehabilitation professionals were recruited. MiL was evaluated wit

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Heip, Tine, and Jochen Van den steen. "Person centred care: good practises in an ambulatory mental healthcare setting." International Journal of Integrated Care 23, S1 (2023): 167. http://dx.doi.org/10.5334/ijic.icic23060.

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Introduction: BW IPSO is an organisation that started out as a variety of small organisations in the late 1970. By offering people with a mental illness the possibility to live in sheltered housing, with the guidance of mental healthcare workers, the organisation intended to improve the quality of life for this population. Over the years the organisation grew, merged and became BW IPSO. We now offer 118 places of supported living, going from group homes, to small appartements provided by the organisation, as well as guiding people in their own (social) home. Description: Throughout the y

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NAKAGAWA, YOSHINORI, RINA YAMADA, and SEIGO NASU. "Characteristics of care-givers and care recipients influencing the impact of paid care services on family care-giver burdens." Ageing and Society 34, no. 8 (2013): 1314–34. http://dx.doi.org/10.1017/s0144686x13000081.

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ABSTRACTIn the last few decades, a number of researchers have attempted to identify the effects of paid care services on alleviating the sense of burden of family care-givers, especially care-givers to people with dementia. However, few researchers have considered the possibility that paid care services alleviate the sense of burden only among those care-givers who possess specific characteristics. Without considering this point, the impact of paid care services would be averaged over an entire sample, and one might overlook the effects on these specific care-givers. With this background, this

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Ehrlich, Ulrike, Nadiya Kelle, Daniela Klaus, and Katja Möhring. "How did the COVID-19 pandemic impact the wellbeing of family care-givers? A longitudinal study of older adults in Germany." Ageing & Society 44, no. 7 (2024): 1533–50. https://doi.org/10.1017/S0144686X22000873.

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Previous research was not able to identify an effect of the COVID-19 pandemic on family care-givers' wellbeing due to cross-sectional data structures, care-giver-specific samples or non-probability sampling designs. In this article, by drawing on longitudinal data from a random and representative sample of the German population aged 40 and older, <strong>the German Ageing Survey (DEAS) 2017 and 2020/21</strong>, we overcome methodological limitations of previous research. We examine the impact of the COVID-19 pandemic on the wellbeing (life satisfaction, depressive symptoms, loneliness) o

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DE LA CUESTA-BENJUMEA, CARMEN, and BRENDA ROE. "The experience of family care-givers and migrant paid care-givers' relief of burden: a contrasted qualitative analysis." Ageing and Society 34, no. 7 (2013): 1219–42. http://dx.doi.org/10.1017/s0144686x13000044.

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ABSTRACTOlder people are increasingly being cared for in the community across Europe. Dependent care in Spain largely remains a private issue involving family carers and migrant women from developing countries. Qualitative research on respite care has contributed to our understanding of respite as a subjective experience. Nonetheless, how care-givers relieve the burden of care is still not fully understood. Migrant care-givers are present in family life but their need for rest remains unseen. The aim of the study presented in this paper was to contrast family care-givers and migrant care-giver

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Thrysøe Hansen, L., L. I. Nielsen, P. Gazerani, and L. Petrini. "“What about me?”: A qualitative explorative study on perspectives of spouses living with complex chronic pain patients." Scandinavian Journal of Pain 16, no. 1 (2017): 173. http://dx.doi.org/10.1016/j.sjpain.2017.04.027.

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Abstract Aims Being a close relative of a chronic pain patient affects family life. No study has been carried out in Denmark to explore relatives’ life experiences and challenges while living with complex chronic pain patients. Hence, the aim of the study was to investigate the experiences of living with chronic pain patients from their spouses’ perspectives. In particular, this study focused on how spouses describe: (i) their everyday tasks and roles as a spouse; (ii) the types of changes and challenges that the pain condition brings into their partnership lives; (iii) a gender difference in

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Fisher, Alinka, Michelle Bellon, Sharon Lawn, and Sheila Lennon. "Identifying Current Practices and Supports in Behaviour Management Following ABI in South Australian Community Settings: A Delphi Study." Brain Impairment 18, no. 2 (2017): 211–25. http://dx.doi.org/10.1017/brimp.2016.36.

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Objectives: To consider the strategies currently used by family care givers to manage challenging behaviour in the community following ABI, and to identify what supports are available that support family care givers in addressing this issue.Research design: Delphi study.Methods: Service providers (n = 8) and family care givers (n = 3) completed a three-round Delphi process with the aim of reaching consensus (75% agreement) regarding research objectives. Round 1 consisted of an open-ended questionnaire in which items were identified; these items were then rated in Round 2 and 3 using a Likert s

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Thèses sur le sujet "Partnership of care givers/family"

Earley, Louise. "Children as familial care givers : the psychological implications." Thesis, University of Warwick, 2001. http://wrap.warwick.ac.uk/89666/.

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This thesis is concerned with children as familial caregivers. To date 'young carers' have received limited attention from researchers, and the current body of literature has mainly developed from the social welfare field. This is in contrast to a vast body of research, which has established the psychological impact of care giving on adults. The first paper critically reviews the concept and research on 'parentification'. This is a systemic/dynamic perspective on the psychological and developmental implications of children's involvement in caring roles. It has been submitted to the Journal of

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Castanon, Léa. "Ρrise en charge institutiοnnelle des persοnnes en situatiοn d'Etat Végétatif Chrοnique οu Etat Ρauci-Relatiοnnel : analyse sοciοlοgique au prisme de la "trajectοire de handicap"". Electronic Thesis or Diss., Normandie, 2024. http://www.theses.fr/2024NORMR126.

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Au travers d’une recherche ethnographique menée dans deux unités (éveil de coma et unité dédiée), la thèse interroge la construction de la trajectoire de handicap des patients en état végétatif chronique ou pauci relationnel. Ces deux états de conscience altérée, entraînent un handicap extrême et une dépendance quasiment totale rendant impossible la participation pleine et entière du patient à sa prise en charge. A la fois présent et absent, ce dernier voit sa trajectoire de handicap se construire au travers d’un partenariat fragile entre les professionnels de santé d’un côté, et les familles

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Bramble, Marguerite Dorothy. "Promoting Family Involvement in Residential Dementia Care: An Education Intervention." Thesis, Griffith University, 2009. http://hdl.handle.net/10072/368110.

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There has been very little empirical research in Australia that examines the role of the family caregiver of the person with dementia in residential care. Nevertheless, both in Australia and overseas, researchers and clinicians recognise that there are benefits for staff, families and their relative with dementia from increased family accessibility, involvement and engagement as clients in care. Client partnerships are defined as dynamic, therapeutic relationships with health professionals that require articulation of common care goals, the exchange of knowledge and clarification of care roles

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Ross, Angela Catherine Dagley John C. "An assessment of anticipatory grief as experienced by family care givers of individuals with dementia." Auburn, Ala, 2008. http://repo.lib.auburn.edu/EtdRoot/2008/SUMMER/Counselor_Education,_Counseling_Psychology,_and_School_Psychology/Dissertation/Ross_Angela_15.pdf.

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Phillips, Susan E. "Care giving, institutionalization and available supports, a study of family care givers of persons with Alzheimer's in central Newfoundland." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape17/PQDD_0014/MQ33824.pdf.

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Bífárìn, Oládayò O., Catherine Quinn, Liz Breen, et al. "Stressors and coping mechanisms of family care-givers of older relatives living with long-term conditions in mainland China: A scoping review of the evidence." Cambridge University Press, 2021. http://hdl.handle.net/10454/18567.

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Yes<br>As the ageing population in China continues to grow, more people will be living with long-term health conditions and require support from family care-givers. This scoping review therefore aims to explore sources of stress and coping mechanisms adopted by care-givers of older relatives living with long-term conditions in mainland China. Literature searches were conducted in English (CINAHL, EMBASE, MEDLINE, PsycINFO and SCOPUS) and Chinese (CNKI, WANFANG DATA, CQVIP and CBM) databases between October and November 2019. The searches focused on the stressors and coping mechanisms utilised

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Adkison, Lesley Ellen. "Establishing Ties: Descriptions of Meaningful Interactions with Health Care Providers from the Perspectives of Family Caregivers of Persons Diagnosed with Moderate to Advanced Dementia." Thesis, Boston College, 2014. http://hdl.handle.net/2345/3788.

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Thesis advisor: Ellen K. Mahoney<br>Purpose: The purpose of this study was to describe meaningful interactions with health care providers (HCPs) from the perspectives of family caregivers of persons with dementia (PWD). A secondary purpose was to understand ways in which family caregivers obtained needed information for managing uncertainty associated with providing care for a PWD. Background: Family members of PWD often assume the caregiver role, but lack preparation for the psychological and practical ramifications of caring for someone with a progressive, terminal illness (Alzheimer's Assoc

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Manning, Jessica Brooke. "An examination of collaborative training methods among participants in the Family Child Care Partnerships Program." Auburn, Ala., 2007. http://repo.lib.auburn.edu/07M%20Theses/MANNING_JESSICA_1.pdf.

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Burbach, Frank Robert. "Developing systemically-oriented secondary care mental health services." Thesis, University of Plymouth, 2013. http://hdl.handle.net/10026.1/1599.

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Research has indicated that offering support and services for people who experience mental health problems and their families is a complex and contested area. Despite the controversies surrounding therapeutic interventions with families, it has now been recognised that relatives and other supporters of people with mental health problems should be included in their care. Whole- family interventions and partnership working with carers and families is now central to secondary care UK mental health policies and clinical practice guidelines. However, for many families/ carers this remains an aspira

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Povilonytė, Ieva. "Emigracijos įtaka mokyklos ir šeimos partnerystei." Master's thesis, Lithuanian Academic Libraries Network (LABT), 2008. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2008~D_20080924_174818-95568.

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Tėvų emigracijos įtaka šeimos ir mokyklos bendradarbiavimui – aktuali ir mažai nagrinėta tema Lietuvoje. Šiuo metu migracijai skiriamas didelis dėmesys, nes tai nėra vien socialinė, ekonominė ar demografinė problema. Nereikia pamiršti, jog situacija, kai tėvai dėl tam tikrų priežasčių išvyksta į kitą šalį, dažnai sukelia neigiamas pasekmes vaiko fizinei bei emocinei būsenai. Tai yra problema, kurios vienas iš aspektų – nutrūkstantis mokyklos ir šeimos bendradarbiavimas. Darbo tikslas - apibūdinti šiuolaikinę šeimos ir mokyklos partnerystės sampratą, bei atskleisti emigracijos problemos pedagog

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Livres sur le sujet "Partnership of care givers/family"

J, Grieco Anthony, ed. Family partnership in hospital care: The cooperative care concept. Springer Pub. Co., 1994.

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Peter, Marsh. Leaving care in partnership: Family involvement with care leavers. Stationery Office, 1999.

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Peter, Marsh. Leaving care in partnership: Family involvement with care leavers. Stationary Office, 1999.

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Sue, Owen, National Children's Bureau, and National Children's Bureau. Early Childhood Unit., eds. Ambiton for change: Partnership, children and work. National Children's Bureau, 2000.

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(Firm), Mitra and Associates, and MEASURE Evaluation Project, eds. 2001 urban family health partnership evaluation survey: Household survey report. Mitra and Associates, 2003.

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B, Gorman John. Child care background checks: How to effectively protect your child from dangerous baby sitters, nannies, and other care givers. Gorman Graphics, 1993.

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Jamieson, Ann. Ambit[i]on for change: Partnership, children, and work. National Children's Bureau, 2000.

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Initiative, Massachusetts Governor's Day Care Partnership. Partnerships for day care: Final report of the Governor's Day Care Partnership Initiative. Governor's Office of Human Resources, Commonwealth of Massachusetts, 1987.

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Siobhán, Bogues, Lindsay Brenda, and Foyle Health and Social Services Trust., eds. Partnership Care West: Evaluation of the Family Support Service Foyle (Waterside/Limavady). Foyle Health and Social Services Trust, 1998.

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Educational Resources Information Center (U.S.), ed. AHEAD Outreach: Where the child is, the services are: home, child care, hospital/clinical services to infants, toddlers, and young children with disabilities and their care givers : final report. SKI-HI Institute, Dept. of Communicative Disorders, Utah State University, 2000.

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Chapitres de livres sur le sujet "Partnership of care givers/family"

Višnjić Jevtić, Adrijana. "Models of Family-School Partnership: Who Is in Power When We Care for the Children We Share?" In International Perspectives on Early Childhood Education and Development. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-38762-3_6.

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AbstractIn this chapter, three models that try to explain the collaborative relations between parents and ECEC teachers are analysed. McAllister Swap models discuss interactions between parents and professionals based on beliefs, expectations, and involvement strategies. Epstein’s Six Types of Parental Involvement are considered through the prism of involvement as a potentially passive position. It is questioned whether in this model the parents are involved by someone, or they have the option of choosing to participate, or not. Hornby’s model of parental participation is considered in relatio

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Parton, Nigel. "Child Care, Prevention and Partnership." In Governing the Family. Macmillan Education UK, 1991. http://dx.doi.org/10.1007/978-1-349-21441-9_2.

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Brown, Erica. "Holistic Care - Family Partnership in Practice." In Care Planning in Children and Young People's Nursing. John Wiley & Sons, Ltd,., 2013. http://dx.doi.org/10.1002/9781118785324.ch10.

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de Lima, Maria Eduarda Batista, Patrocinio Ariza-Vega, Aline Tavares Domingos Forte, and Stefano Eleuteri. "Family Partnerships, Patient and Carer Education and Support." In Perspectives in Nursing Management and Care for Older Adults. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-33484-9_15.

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AbstractThe involvement of the family, friends, and other people who are important to the patient has always been at the centre of any person-centred care process. Following a fragility fracture, many patients want their family and significant others to be involved in their care, both during hospitalisation and after discharge, and it is often expected that families will provide or lead ongoing care after discharge.It is well documented that postoperative functional decline is influenced by a great complexity of factors and that care aimed at preserving patients’ maximum autonomy, improving th

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Wright, Natalie, Leighann Ness Wilson, Anastasia Tyurina, Jane Harnischfeger, Sarah Johnstone, and Judy Matthews. "‘It Takes a Village’: The Power of Conceptual Framing in the Participatory Redesign of Family-Centred Care in a Paediatric Intensive Care Unit." In How Designers Are Transforming Healthcare. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-6811-4_3.

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AbstractFamily-centred care (FCC) is a global approach to the planning, delivery, and evaluation of safe, quality health care that is grounded in mutually-beneficial partnerships among health care providers, patients, and families. This perspective not only relates to direct care interactions, but also to quality improvement, safety initiatives, education of health professionals, research, facility design, and policy development. This chapter presents and discusses the process and outcomes of a truly collaborative and values-led participatory design quality improvement project undertaken by th

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Howard, Christopher. "Daily Care." In Who Cares. Oxford University PressNew York, 2022. http://dx.doi.org/10.1093/oso/9780190074456.003.0010.

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Abstract Many people are unable to perform everyday tasks like getting dressed, preparing meals, or bathing. Young children belong in this group, as do adults with disabilities that range from mild to severe. Historically, family members have been the primary givers of daily care; most have been women and unpaid. Over time, paying other people to care for the young, the old, and the disabled has become more common. However, most of the poor and near poor cannot afford a child-care center or nursing home on their own. If they work unpredictable hours, evenings, or weekends, affordable care is e

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Kaufmann, Beatrice, Anouk Haldemann, Christopher Lueg, Loraine Olalia, Friederike Thilo, and Kerstin Denecke. "Can We Do Better than Gesturing? Requirements for a Digital Communication Aid to Support Non-Verbal Communication in Paediatric Emergency Care." In MEDINFO 2021: One World, One Health – Global Partnership for Digital Innovation. IOS Press, 2022. http://dx.doi.org/10.3233/shti220254.

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Providing urgent and emergency care to migrant children is often hampered or delayed. Reasons for this are language barriers when children, and their care givers, don’t speak any of the languages commonly spoken in Switzerland, which include German, French, Italian, and English. By a participatory design process, we want to develop a novel image-based digital communication aid tailored to the needs of migrant patients and nurses within Swiss paediatric clinics.

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Nedelsky, Jennifer. "Introduction." In Part-Time for All. Oxford University PressNew York, 2023. http://dx.doi.org/10.1093/oso/9780190642754.003.0001.

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Abstract The introduction provides an overview of the book. The premise is that care involves work and good work involves care. We offer a diagnosis of the interconnected problems of work and care: inequality for care-givers, family stress, time scarcity, and the care/policy divide that generates policy makers ignorant of care and excludes care givers as policy makers. It outlines the solution of new norms: no one does paid work for more than 30 hours a week, and everyone contributes roughly 22 hours of unpaid care to family, friends, or their chosen community of care. The challenges of norm t

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Lowe, N. V., G. Douglas, E. Hitchings, and R. Taylor. "18. Care and Supervision." In Bromley's Family Law. Oxford University Press, 2021. http://dx.doi.org/10.1093/he/9780198806691.003.0018.

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The Children Act 1989 places considerable importance on local authorities working in partnership with families and the avoidance wherever possible of court proceedings. However, the Act also makes provision, in the form of care and supervision orders, for compulsory measures to be taken to safeguard and promote children’s welfare. This chapter focuses on care and supervision orders. It covers the initiation of proceedings; the threshold criteria, which refers to conditions set out by s 31(2) that must be satisfied before a care or supervision order may be made; the ‘welfare stage’, where the c

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Luke, Michael J. "Social Care Interventions." In Social Drivers of Health. American Academy of PediatricsItasca, IL, 2025. https://doi.org/10.1542/9781610027922-8.

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Health systems interested in screening for health-related social needs must first ensure they are equipped with accessible and family-centered intervention strategies to address any identified needs. Several factors, such as variability in severity of need among families and differences in resource availability based on geography, serve as considerable barriers to designing and streamlining social needs interventions. Some common strategies used in health care to overcome these barriers and address families’ needs include aggregated resource lists, in-person support to navigate these resources

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Actes de conférences sur le sujet "Partnership of care givers/family"

Repciuc (Jucan), Elena. "Family and Kindergarten - the Partnership for Education." In ATEE 2020 - Winter Conference. Teacher Education for Promoting Well-Being in School. LUMEN Publishing, 2021. http://dx.doi.org/10.18662/lumproc/atee2020/27.

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This paper presents both theoretical and practical aspects of the significance of this kindergarten-family partnership with the mission to inform both teachers and parents about the importance of collaboration and to offer some suggestions by which we can make the communication between these two parts. The main objective underlying this paper is to study in detail the partnership between kindergarten and family and to analyze the reasons why this partnership is not fully realized in order to facilitate better communication between these two parties. The paper is structured in 3 chapters as fol

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Frizzola, Meg, Elissa Miller, Juliana Hayman, and Carly Levy. "Picu and Palliative Care Partnership to Standardize Family Meetings and Decrease Icu Readmission Rates." In Selection of Abstracts From NCE 2016. American Academy of Pediatrics, 2018. http://dx.doi.org/10.1542/peds.141.1_meetingabstract.388.

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"Partnership with a Family Having a Child with Mental Disorders—strategy for Quality Improvement in Health Care." In Congress on mental health meeting the needs of the XXI century. Gorodets, 2016. http://dx.doi.org/10.22343/mental-health-congress-compendium20-23.

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Richmond, Deborah. "Empowered Mobility: Supply Chain Thinking for Youth in Foster Care." In 2016 ACSA International Conference. ACSA Press, 2016. http://dx.doi.org/10.35483/acsa.intl.2016.29.

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The application of global container logistics to high mobility children, such as those in foster care, asks designers to consider an empathic, human-centered approach to an institutionalized system of involuntary mobility, which can result in as many as 3-4 family “placements” per year for some children. In spite of grim statistics for youth in foster care related to graduation, teen pregnancy, drug use and imprisonment, these children develop many positive resiliencies around adaptability, emotional intelligence, empathy and efficiency. Working with a non-profit serving youth in foster care i

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Pacheco, Andre G. C., Clayton Oliveira Vicente, Eduarda Pylro Magesk, Gabriel Schettino Lucas, Guilherme Teixeira Caldana, and Patricia H. L. Frasson. "SADE: Software de Análise Dermatológica - Um sistema de coleta, gerenciamento e triagem de lesões de pele." In Anais Estendidos do Simpósio Brasileiro de Sistemas Multimídia e Web. Sociedade Brasileira de Computação - SBC, 2023. http://dx.doi.org/10.5753/webmedia_estendido.2023.235905.

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Skin cancer is a global public health challenge, accounting for approximately one-third of cancer diagnoses worldwide. The state of Espírito Santo has tens of thousands of inhabitants of European descent. Most of them have fair skin and are engaged in family farming, often exposed to the sun. The combination of this vulnerable phenotype with such sun exposure results in a high incidence of skin cancer in the state. Since 1987, the Federal University of Espírito Santo has maintained a dermatological and surgical assistance program, providing free care to the most vulnerable population. Starting

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Gričnik, Ana Marija, Matjaž Mulej, and Simona Šarotar Žižek. "Sustainable Human Resource Management." In 7th FEB International Scientific Conference. University of Maribor, University Press, 2023. http://dx.doi.org/10.18690/um.epf.3.2023.35.

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Sustainable HRM (SHRM) is a new approach to people management, focusing on long-term HRM, regeneration, and renewal. It helps firms attract and retain high-quality employees: by integrating SHRM practices into their employee value proposition, firms establish unique, attractive employer brands. Socially Responsible HRM, Green HRM, Triple Bottom Line HRM, and Common Good HRM are types of SHRM. Especially these characteristics of SHRM matter: Long-term orientation, care for employees, environment, profitability, employee participation and social dialogue, employee development, external partnersh

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Olteanu, Radu Lucian, and Gabriel Gorghiu. "INCREASING THE STUDENTS’ INTEREST IN SCIENCE BY IMPLEMENTING A SCIENCE ACTION DEDICATED TO PLASTICS BIODEGRADABILITY." In 5th International Baltic Symposium on Science and Technology Education. Scientia Socialis Press, 2023. http://dx.doi.org/10.33225/balticste/2023.162.

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Science actions represent specific initiatives and demarches that involve investigation, experimentation, and even research, for raising the interest of the young generation in science, through particular approaches of STEM education. Important topics are promoted to students in various approaches, addressing nowadays problems, answering scientific questions, or trying to make them aware of sensible issues. In this respect, the topic of plastics biodegradability embraced the clothes of a Science action, a format based on the Care-Know-Do model, proposed in the frame of the CONNECT project. Hav

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Lavilla, KM, J. Teal, B. Schausberger, et al. "Safe motherhood and childhood in Sierra Leone: key findings from mixed-methods health-seeking behaviour study." In MSF Scientific Days International 2022. MSF-USA, 2022. http://dx.doi.org/10.57740/8sd6-2h56.

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INTRODUCTION MSF and the MoHS implemented a partnership model of free and accessible maternal and child healthcare at primary and hospital-level health facilities in Tonkolili District, Sierra Leone, in order to reduce barriers to care and improve health outcomes. We conducted a health-seeking behaviour (HSB) study in 2021 to evaluate impact and change since a previous HSB study conducted in 2016/17. We also compared MSF-supported primary health unit (PHU) catchment areas with MSF-unsupported PHU’s. In addition, we explored adolescent reproductive health, family planning, and female genital mu

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Rapports d'organisations sur le sujet "Partnership of care givers/family"

Oza, Shardul, and Jacobus Cilliers. What Did Children Do During School Closures? Insights from a Parent Survey in Tanzania. Research on Improving Systems of Education (RISE), 2021. http://dx.doi.org/10.35489/bsg-rise-ri_2021/027.

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In this Insight Note, we report results of a phone survey that the RISE Tanzania Research team conducted with 2,240 parents (or alternate primary care-givers) of primary school children following the school closures in Tanzania. After the first case of COVID-19 was confirmed in Tanzania on 16 March 2020, the government ordered all primary schools closed the following day. Schools remained closed until 29 June 2020. Policymakers and other education stakeholders were concerned that the closures would lead to significant learning loss if children did not receive educational support or engagement

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Mir, Ali M., Zeba Sathar, Iqbal Shah, Rehan Niazi, Tahira Parveen, and Susheela Singh. Safeguarding women's health: Trends, inequities, and opportunities in Pakistan's abortion and post-abortion care services. Population Council, 2024. http://dx.doi.org/10.31899/sbsr2024.1039.

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This report presents the findings of a comprehensive study on abortion and post-abortion care in Pakistan, conducted in 2023 by the Population Council in partnership with the Guttmacher Institute. The study addresses a critical need for updated information on women's reproductive health in Pakistan, a country facing significant challenges including a high population growth rate (2.55% per annum), low contraceptive use (34% for any method, 23.4% for modern methods), and a high unmet need for family planning (17.3%). The study is the third of its kind since 2002, building on previous research co

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Magnaye, Andrew. Employed Caregivers in Canada: Infographic Compilation. The Vanier Institute of the Family, 2023. https://doi.org/10.61959/pvfy6434e.

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We are pleased to announce the release of our latest co-publication on employed caregivers in Canada, produced in partnership with Research on Aging, Policies and Practice (RAPP). This compilation includes six infographics that each provide insight into various aspects of caregiving and on the value and contributions of family caregivers across Canada. The infographics, which were created by Andrew Magnaye, Choong Kim, Jacquie Eales, and Janet Fast, utilize data from Statistics Canada’s 2018 General Social Survey on Caregiving and Care Receiving to update key indicators on working caregivers.

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Hossain, Sharif M. I., Shongkour Roy, Sigma Ainul, Abdullah Al Mahmud Shohag, A. T. M. Rezaul Karim, and Ubaidur Rob. Assessing effectiveness of a person-centered group ANC-PNC model among first-time young mothers and their partners for improving quality and use of MNCH-FP services. Population Council, 2022. http://dx.doi.org/10.31899/sbsr2022.1041.

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This baseline report is part of an operations research project “Healthy Women, Healthy Families (HWHF): Shustha Ma, Shustha Poribar” led by Management Sciences for Health (MSH) in partnership with BRAC, SCOPE, and the Population Council. The project aims to improve quality and increase utilization of maternal, newborn, and child health (MNCH) and family planning (FP) services and information for young mothers-to-be, first-time mothers (FTMs) aged 15-24, and their partners in the urban municipality of Tongi, Gazipur District, Bangladesh, through a group antenatal care ANC-PNC approach. The obje

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Policy brief—Safeguarding women's health: Trends, inequities, and opportunities in Pakistan's abortion and postabortion care services. Population Council, 2024. http://dx.doi.org/10.31899/sbsr2024.1040.

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Pakistan is experiencing critical reproductive health issues driven by a high population growth rate of 2.55% per year, low contraceptive use (34% for all methods, 23.4% for modern methods), and a significant unmet need for family planning (17.3%). Low contraceptive use and high unmet need for family planning contribute to high rates of unintended pregnancies which often result in unsafe abortions and postabortion complications. This policy brief presents the findings of a comprehensive study on abortion and postabortion care in Pakistan. The study was conducted in 2023 by the Population Counc

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Involving youth in the care and support of people affected by HIV and AIDS. Population Council, 2003. http://dx.doi.org/10.31899/hiv2003.1016.

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Young people in Zambia who were trained to provide care and support to individuals and families affected by AIDS have proven to be a vital resource to their communities. In a country where adult HIV prevalence is 13 percent among males and 18 percent among females, communities are seeking new ways of helping those infected and affected by the disease. As the needs of people living with HIV and AIDS (PLHA) and orphans and vulnerable children continue to escalate, results from an intervention study by the Horizons Program, in partnership with Care International and Family Health Trust, provide a

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Global Food 50/50 Report 2023/2024. International Food Policy Research Institute (IFPRI), 2024. http://dx.doi.org/10.56649/ddxd8983.

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Global Food 50/50 (GF5050) is a partnership between Global Health 50/50 (GH5050), the International Food Policy Research Institute (IFPRI), and UN Women. The GF5050 Report monitors progress and holds food system organizations accountable for achieving intersectional gender equality in leadership, adopting gender-equitable internal workplace policies, and implementing strategies that advance progress toward gender-just and equitable food systems. The 2023/2024 Report presents findings on the workplace policies for care and family leave from 51 global organizations active in the global food syst

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