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Thematische Bibliographien / Partnership of care givers / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Partnership of care givers“

Autor: Grafiati

Veröffentlicht am 5. April 2025

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Mawarni, Ellis, Dachriyanus Dachriyanus, Esthika Ariany Maisa, and Jufri Al Fajri. "Gambaran Pengetahuan Inter Professional Collaboration Pada Profesional Pemberi Asuhan Di Rumah Sakit Khusus Propinsi Jambi: Kajian." Jurnal Ilmiah Universitas Batanghari Jambi 19, no. 2 (2019): 416. http://dx.doi.org/10.33087/jiubj.v19i2.676.

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Interprofessional collaboration (IPC) between nurses and doctors is associated with good outcomes for patients, especially in hospitalizations. Different professional cultures can be a barrier to nurses and doctors in an IPC effective and efficient. Effective IPC is important to ensure patient safety. To analyze how the image of Professional Care Givers is different in implementing IPC at Jambi Special Hospital. The research was cross-sectional, the population were nurses, doctors, pharmacists and nutritionists in Jambi Province Special Hospital 105 samples. Sampling with total sampling. AITCS

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Baldwin, Dana. "A Joint Demonstration Project to Improve the Care of Patients with Dementia: A Partnership Between a Staff Model HMO and the Alzheimer's Association." Practicing Anthropology 20, no. 2 (1998): 17–18. http://dx.doi.org/10.17730/praa.20.2.42p6px0w77htt777.

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I am part of a multi-disciplinary team composed of researchers from Kaiser Permanente, the country's largest staff model Health Maintenance Organization (HMO) and the Los Angeles chapter of the Alzheimer's Disease and Related Disorders Association. This team has designed a demonstration service delivery system to enhance the quality of care given to dementia patients and their care givers. If the demonstration project is successful, it may be expanded throughout the Kaiser system. After completing my Ph.D. in medical anthropology at UCLA, I worked as a consultant at the Rand Corporation then h

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Swinnen, Katja, and Leia Vrancken. "Enhancing transmural continuity of care for vulnerable patients with kidney problems. A mixed-methods multi-stakeholder needs-assessment." International Journal of Integrated Care 23, S1 (2023): 130. http://dx.doi.org/10.5334/ijic.icic23051.

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Summary: Research on supporting the (in)formal caregiver, in enabling autonomy and empowering of persons with a chronic kidney disorder and creating a bridge between primary care and specialized care in hospital settings.  Background: Almost half (48%) of hospital readmissions is due to a lack of continuity of care ,e.g. no discharge conversation, poor communication at discharge, lack of patient education and no patient empowerment, a lack of information flow between the hospital setting and primary care, … Especially vulnerable patients with e.g. low health literacy suffer from a not op

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Rehman, Raza ur, Saadia Quraishy, and Naim Siddiqi. "POSTGRADUATE COMMUNITY PSYCHIATRY TRAINING IN PAKISTAN." Journal of Pakistan Psychiatric Society 19, no. 02 (2022): 44–47. http://dx.doi.org/10.63050/jpps.19.02.158.

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Closure of large psychiatric hospitals across UK, Europe and the United States has shifted the services for the care of psychiatric patients to general hospitals, community based public and private facilities and social sector organizations. Underpinning the process of deinstitutionalization and the development of community psychiatric services was the ethos of providing seamless, flexible services close to where people lived, led by their needs and with involvement of them and their care givers. In Pakistan, in-patient psychiatric facilities are scarce and community psychiatry is still in its

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Mailani, Robit Altom, and Risdiana Himmati. "Kerjasama bagi hasil ayam potong untuk meningkatkan kesejahteraan bagi pelaku usaha." Journal of Economics Research and Policy Studies 2, no. 2 (2022): 60–71. http://dx.doi.org/10.53088/jerps.v2i2.375.

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Chicken farming is a form of agribusiness that is capital intensive. Broiler chicken is one of the farms if it is developed to have good prospects. Businesses in the field of animal husbandry in the form of broiler cultivation can establish partnerships. A partnership is a form of cooperation that applies profit sharing. The broiler cooperation program aims to establish mutually beneficial and reinforcing business cooperation and mutual trust between farmers and the core party (business partners or investors). Qualitative analysis was used in this study with a descriptive qualitative model. Th

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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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Perkins, Neil, and David James Hunter. "Health and Wellbeing Boards: a new dawn for public health partnerships?" Journal of Integrated Care 22, no. 5/6 (2014): 220–29. http://dx.doi.org/10.1108/jica-07-2014-0030.

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Purpose – The purpose of this paper is to consider the effectiveness of partnership working in public health and draws on a systematic review of public health partnerships and original research conducted by the authors. It then considers in the light of research evidence whether the recently established Health and Wellbeing Boards (HWBs) under the 2012 Health and Social Care Act will help agencies to work together more effectively to improve population health or will go the way of previous initiatives and fall short of their original promise. Design/methodology/approach – The paper is based on

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Ariesti, Ellia, Monika Luhung, and Eli Lea Widhia Purwandhani. "PELATIHAN CAREGIVER LANSIA TENTANG SKRINING STATUS GIZI MENGGUNAKAN THE MINI NUTRITIONAL ASSESSMENT (MNA)." SELAPARANG: Jurnal Pengabdian Masyarakat Berkemajuan 6, no. 3 (2022): 1149. http://dx.doi.org/10.31764/jpmb.v6i3.9300.

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ABSTRAKLansia merupakan kelompok khusus yang rentan dan berisiko mengalami berbagai permasalahan terkait kesehatan mereka. Di LKS-LU Pangesti Lawang 21 lansia pernah terpapar Virus Covid 19, sehingga sangat diperlukan perhatian khusus terhadap kesehatan lansia, terutama dalam upaya mempertahankan imunitas, misalnya melalui asupan nutrisi adekuat. Indikator nutrisi adekuat dapat diketahui melalui skrining menggunakan the Mini Nutritional Assessment (MNA). Tujuan kegiatan Program kemitraan Masyarakat (PkM) ini adalah melatih dan meningkatkan keterampilan care giver lansia melakukan skrining stat

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McCann, Warren. "Redeveloping Primary Health and Community Support Services in Victoria." Australian Journal of Primary Health 6, no. 4 (2000): 36. http://dx.doi.org/10.1071/py00032.

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Why Primary Care Reforms?: It gives me very great pleasure to have been asked to speak at this major international Conference about redeveloping primary health and community support services in Victoria. While opening the Conference, the Victorian Minister for Health, the Honourable John Thwaites, launched the Primary Care Partnership Strategy which is one of the most ambitious and far reaching primary health and community support reform agendas in Australia.

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Stephanos, Francis. "Power and Partnership Conference: Challenging the Power Structure." Global South Theological Journal 2, no. 2 (2024): 35–48. http://dx.doi.org/10.57003/gstj.v2i2.11.

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God, the creator and the proprietor of every living and non-living thing, is the source of power and authority, which he delegates to humans to exercise authority and control, for proper use and care of all God’s creation, placed at their disposal and for the well-being of humanity. But with power comes the misuse of power as evidenced is power sharing struggles, misuse of power by the governmetn and misuse of pwoer by the church. In the palce of the exercise of pwoer, Jesus gives us the servanthood partnership--partnership which is expressed in compassion, humility, obedience, and a genuine s

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Sunderland, Ronald H. "The Dignity of Servanthood in Pastoral Care." Journal of Pastoral Care & Counseling: Advancing theory and professional practice through scholarly and reflective publications 57, no. 3 (2003): 269–79. http://dx.doi.org/10.1177/154230500305700303.

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Servanthood is a dominant image of ministry in both Jewish and Christian scriptures, and poses a rich source of material from which to address the theme of human dignity from the perspective of pastoral care. The biblical concept of servanthood, which defines the nature of the pastoral relationship and dignifies the personhood of the care recipient, suggests an approach to the issues of vulnerability of both giver and receiver of care, and proposes that the caring relationship is best conceived as a partnership to which each participant brings gifts. The servant theme implies addressing the no

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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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Ryckman, Aurelie. "A collaboration between first- and second-line healthcare for persons with a disability in Flanders to strengthen quality of care, continuity of care and affordability of care." International Journal of Integrated Care 23, S1 (2023): 391. http://dx.doi.org/10.5334/ijic.icic23488.

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The introduction of personal financing within the disability sector, in Flanders, in 2017, created the opportunity to enter into broader collaborations with other professional services. This allows us to strengthen the quality of care and support for people with disabilities. We therefore started a collaboration between first and second line healthcare. This collaboration is based on 3 major pillars, quality of care, continuity of care and affordability of care. With the introduction of personal financing in the disability sector, care focusses more on the person with a disability. The adult p

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Thomas, Anne. "Stranger danger! What’s the real challenge in integration?" Journal of Integrated Care 23, no. 4 (2015): 194–205. http://dx.doi.org/10.1108/jica-07-2015-0029.

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Purpose The purpose of this paper is to illustrate the complexities involved in delivering seamless patient-centred care across organisational boundaries. There is particular focus on how working with an organisation outside the public sector challenges the ideology of those involved, thereby hindering progress. It will explore the challenges and solutions to delivering a service and discuss the key components of success. It will investigate the theory of partnership working and balance the importance of the emotional investment and understanding with leadership and project management. Design/

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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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Iftikhar, Danyal, Rabia Farooqi, Shahzad Waheed Qureshi, Amina Tariq, Amna Mehwish Ikram, and Adeel Haidar. "Assessment of Parental self-management of epileptic pediatric in terms of adherence of antiepileptic drugs." Pakistan Journal of Medical and Health Sciences 15, no. 7 (2021): 1587–89. http://dx.doi.org/10.53350/pjmhs211571587.

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Aim: To assess the parental self-management of epileptic pediatric in terms of adherence of antiepileptic drugs Methodology: A descriptive cross-sectional study was conducted in Children Complex Hospital of Multan. Convenient sampling technique was used to collect the data from included population, care giver of epilepticus children. Reliability checked by Cronbach alpha which was 0.71. Data was analyzed in SPSS 25, to get percentage and frequency. Results: The majority of the responses were agree 86(81.9%) on the doctors/nurses fully explained seizures/epilepsy (diagnosis). 10(9.5%) were stro

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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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Robinson, Lianne, Mosunmola Fapohunda, Abiemwense Giwa-Osagie, Bolanle Ogunleye, Oritseweyinmi Okhiria, and Olalekan Aina. "The African and Caribbean Doctors Buddy Group (ACDBG) at HPFT- Hertfordshire Partnership University NHS Foundation Trust." BJPsych Open 9, S1 (2023): S108. http://dx.doi.org/10.1192/bjo.2023.313.

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AimsThere are increasing amounts of documented evidence that Black and Ethnic Minority (BME) NHS staff are more likely to face exclusion and discrimination. The MWRES- Medical Workforce Race Equality Standards Report details the disadvantages faced by BME doctors in the NHS. This piece of work shows a strategy to support doctors of African and Caribbean origin working in HPFT. Launched in 2021, the HPFT African and Caribbean Doctors Buddy Group (ACDBG) is a group for all doctors of any grade working in HPFT from African and Caribbean backgrounds. The group aims to bring together doctors of the

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CHEN, CHEN-FEN. "Insiders and outsiders: policy and care workers in Taiwan's long-term care system." Ageing and Society 36, no. 10 (2015): 2090–116. http://dx.doi.org/10.1017/s0144686x15001245.

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ABSTRACTAs in many developed countries, foreign care-givers have made up a short-term labour force to help shoulder the responsibilities of older adult care in Taiwan since 1992. This study uses the dual labour market and the occupational segregation theoretical frameworks and a mixed-method approach to examine whether foreign care-givers are supplementary or have replaced Taiwanese care-givers in Taiwan's long-term care (LTC) industry, and to understand better the status of care workers and their influx into the secondary labour market. As of 2012, 189,373 foreign workers joined the care serv

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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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JACOBS, MARIANNE, THEO VAN TILBURG, PETER GROENEWEGEN, and MARJOLEIN BROESE VAN GROENOU. "Linkages between informal and formal care-givers in home-care networks of frail older adults." Ageing and Society 36, no. 8 (2015): 1604–24. http://dx.doi.org/10.1017/s0144686x15000598.

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ABSTRACTIn ageing societies, policy makers aim for more contact between informal and formal care-givers as it may enhance the quality of care. So far, the linkage between formal and informal care-givers is generally studied from a one-sided or a single dyadic perspective, without taking into account that care networks of community-dwelling older adults often exist of multiple informal and formal care-givers. The current study examines discussion of care between all potential informal–formal care-giver dyads in a care network, and relates this to characteristics of the older care recipient, the

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G, Umesh, Asokan T.V., Roselin V, and Sri Santhanakrishnan V. V. "Cross-Sectional Study on Stigma among Care Givers of Patients with Mental Illness in Kanchipuram District, Tamil Nadu." Journal of Evidence Based Medicine and Healthcare 8, no. 28 (2021): 2484–88. http://dx.doi.org/10.18410/jebmh/2021/460.

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BACKGROUND Stigma experienced by caregivers of patients with mental illnesses remains unnoticed. This study was conducted to evaluate the stigma perceived by the care givers of patients with various mental illnesses and the factors associated with stigma. METHODS This cross-sectional study was conducted among the care givers of patients with mental illnesses who accompanied the patients to the outpatient department (OPD) of Psychiatry in Meenakshi Medical College Hospital and Research Institute, from January 2017 to March 2017. A total of hundred care givers were included in the study. All car

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Mainwaring, Debra. "Educational Psychologists as advocates of children in out of home care: An innovative program model that empowers young people and the adults who support them." Educational and Child Psychology 31, no. 1 (2014): 101–23. http://dx.doi.org/10.53841/bpsecp.2014.31.1.101.

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Life Without Barriers, a specialist foster care agency, are funding a Collaborative Education Program in partnership with Edmund Rice Education Australia Youth +. This paper aims to share some of the practice that gives a voice to the children and young people who have experienced trauma, abuse and neglect and have been placed in out of home care. Casework illustrations serve to reveal how the voice of the child is included in measures of participation, well-being and achievement that inform their Education Support Plans. Given the evidence of the impact of trauma on language development non-v

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Huang, Chiung-Yu. "Informal Female Caregivers of Older Adults with Dementia in Taiwan." Californian Journal of Health Promotion 2, no. 3 (2004): 53–66. http://dx.doi.org/10.32398/cjhp.v2i3.880.

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Family care givers providing a major portion of care giving often experience stress related to the negative consequences for their health. Female care givers often more heavily involved care giving activities than males. Care givers’ gender studies have seldom conducted in Taiwan. The purpose of this study was to explore the relationship of demographic factors and coping on health of female care givers of older adults with dementia in Taiwan. In addition, whether coping mediated or moderated the relationship between stress and care giver’s health was also examined. Lazarus and Folkman’s Stress

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Bentwich, Miriam Ethel, Ya'arit Bokek-Cohen, and Nomy Dickman. "How figurative language may be related to formal care-givers’ person-centred approach toward their patients with dementia." Ageing and Society 39, no. 12 (2018): 2653–70. http://dx.doi.org/10.1017/s0144686x18000685.

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AbstractPerson-centred care that respects a patient's personhood is the gold standard in dementia care, which is often difficult to achieve given the complexity of caring for people with dementia. This article delves into the narration style of formal care-givers from a variety of ethno-cultural backgrounds in search of linguistic cues that may be related to their emphasis on a person-centred approach to care. A qualitative study, using a discourse analysis of semi-structured interviews with 20 formal care-givers in an institutional setting, was employed. The care-givers fell into three groups

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Wells, Y. D., A. F. Jorm, F. Jordan, and R. Lefroy. "Effects on Care-Givers of Special Day Care Programmes for Dementia Sufferers." Australian & New Zealand Journal of Psychiatry 24, no. 1 (1990): 82–90. http://dx.doi.org/10.3109/00048679009062889.

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Two groups of care-givers to dementia sufferers were interviewed to assess their psychological symptoms and the behaviour problems of the dementia sufferers. The first group were using special dementia day care while the second group were about to begin using it. The second group were re-interviewed three months later. Therefore two comparisons could be made; a with/without day care comparison and a before/after admission to day care comparison. Care-givers had a high level of psychological symptoms which were not significantly reduced by using day care. Full-time institutional care did reduce

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Özen, Yelda. "Body work and later-life care in Turkey: a qualitative study of paid and unpaid carers of older people." Ageing and Society 40, no. 10 (2019): 2106–27. http://dx.doi.org/10.1017/s0144686x19000989.

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AbstractThe ageing population of Turkey has brought later-life care into question. Family care remains most prevalent, but institutional, paid and professional care are increasing. Literature in Turkey has focused on the medical or social policy aspects but not care-givers’ experiences, nor how the care is performed. This study aims to illuminate care-givers’ experiences using qualitative methods, through in-depth interviews in Ankara with 19 care-givers providing home care for people aged 65 and over. Commonalities and differences were revealed among unpaid family care-givers, paid care-giver

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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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Farberman, Harvey A., Stephen J. Finch, Beverly P. Horowitz, Abraham Lurie, Richard Morgan, and Jaimie Page. "A Survey of Family Care Giving to Elders in New York State: Findings and Implications." Care Management Journals 4, no. 3 (2003): 153–60. http://dx.doi.org/10.1891/cmaj.4.3.153.57524.

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It is estimated that there are 734,400 care giver households in New York State (9.6% [±] 0.8% of all households). Categorization of all care givers on a 5 level “intensity of care” measure reveals that, on average, care givers provide 22.1 hours of care per week. Highest intensity level 5 care givers (9.2% of all care givers), provide, on average, 88 hours of care per week and account for 36.3% of all care giving. The annualized market contribution of all care givers to the NYS health care system is estimated at between $7.5 and $11.2 billion dollars. The combination of care levels 4 and 5 con

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Zelewsky, Marianne G., and Emily P. Deitrick. "Rx for Care Givers: Respite Care." Journal of Community Health Nursing 4, no. 2 (1987): 77–84. http://dx.doi.org/10.1207/s15327655jchn0402_4.

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Heinert, Sara, Marina Del Rios, Arjun Arya, et al. "The CHAMPIONS NETWork: Training Chicago High School Students as Health Advocates to Improve Health Equity." Health Promotion Practice 20, no. 1 (2018): 57–66. http://dx.doi.org/10.1177/1524839918757755.

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In Chicago, major disparities exist across ethnic groups, income levels, and education levels for common chronic conditions and access to care. Concurrently, many of Chicago’s youth are unemployed, and the number of minorities pursuing health professions is low. In an effort to eliminate this health equity gap, the University of Illinois at Chicago convened a community–university–hospital partnership to implement the CHAMPIONS NETWork (Community Health And eMPowerment through Integration Of Neighborhood-specific Strategies using a Novel Education & Technology-leveraged Workforce). This inn

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CUSTERS, ANNETTE F. J., YOLANDE KUIN, MARIANNE RIKSEN-WALRAVEN, and GERBEN J. WESTERHOF. "Need support and wellbeing during morning care activities: an observational study on resident–staff interaction in nursing homes." Ageing and Society 31, no. 8 (2011): 1425–42. http://dx.doi.org/10.1017/s0144686x10001522.

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ABSTRACTQuality of life and wellbeing in nursing homes are becoming more important in research and practice. One of the main influences on residents' wellbeing is the interaction with their professional care-givers. The purpose of this study was to explore to what extent care-givers support the residents' needs of relatedness, autonomy and competence, and how this need support is related to wellbeing. Residents and their professional care-givers of four nursing homes in the Netherlands participated in an observational and questionnaire study. Three video-observations of each resident (with dif

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Pereira, Anabela, Joaquim Escola, Vitor Rodrigues, and Carlos Almeida. "Parents’ Perspectives on the Health Education Provided by Clinicians in Portuguese Pediatric Hospitals and Primary Care for Children Aged 1 to 10 Years." International Journal of Environmental Research and Public Health 17, no. 18 (2020): 6854. http://dx.doi.org/10.3390/ijerph17186854.

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This study aimed to analyze parents’ perspectives of the health education practice provided by health professionals to children and parents. This is a descriptive research with a qualitative approach, based on the conceptual framework of health education provided by health professionals to children/young people and families. The selection took place by non-probabilistic sampling of convenience, and was developed with parents/users of health units for pediatric hospitalization and primary health care in northern Portugal. Data were collected using semi-structured interviews with 20 parents from

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Ringer, Thom J., Matthew Wong-Pack, Patricia Miller, et al. "Understanding the educational and support needs of informal care-givers of people with dementia attending an outpatient geriatric assessment clinic." Ageing and Society 40, no. 1 (2018): 205–28. http://dx.doi.org/10.1017/s0144686x18000971.

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AbstractInformal (unpaid) care-givers of older people with dementia experience stress and isolation, causing physical and psychiatric morbidity. Comprehensive geriatric assessment clinics represent an important geriatrician-led model of dementia care. Our qualitative study examined the educational and support needs of care-givers of people diagnosed with dementia at a geriatric assessment clinic, resources used to address those needs and challenges experienced in doing so. We conducted structured thematic analysis of interviews with 18 informal care-givers. Participants’ narratives reflected f

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Gandhi, Priya, Bindu Shaiju, and Eke Lama Tamang. "Patients’ and Care-givers’ Knowledge and Practice regarding Prevention of Complications of Immobilisation with a View to Develop an Information Booklet." Nursing Journal of India CVIII, no. 05 (2017): 206–9. http://dx.doi.org/10.48029/nji.2017.cviii504.

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This study was conducted at a tertiary care hospital with the objectives to assess the knowledge and practice of immobilised orthopaedic patients and their care-givers regarding prevention of complications of immobilisation and to seek relationship between knowledge and practice scores with the selected demographic variables. A quantitative approach with descriptive survey design was used. A semi structured questionnaire, to assess the knowledge and a checklist to assess the practice of both patients and their care-givers were used for data collection. Purposive sampling technique was employed

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Fee, Anne, Sonja McIlfatrick, and Assumpta Ryan. "‘When it faded in her … it faded in me’: a qualitative study exploring the impact of care-giving on the experience of spousal intimacy for older male care-givers." Ageing and Society 41, no. 1 (2019): 29–50. http://dx.doi.org/10.1017/s0144686x19000850.

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AbstractOlder male care-givers play an increasingly important role in informal care-giving, yet they have received little attention in the literature. The aim of this study was to explore the impact of care-giving on the experience of spousal intimacy for older male care-givers. Twenty-four older male care-givers, drawn from a region of the United Kingdom, participated in one-to-one interviews about their care-giving role. Thematic analysis was used to analyse data, and the study was underpinned by theories of masculinity. Three main themes were identified: (a) ‘Impact of care-giving on the ex

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Rady, A., T. Mouloukheya, and E. Ramadan. "Post traumatic stress disorder symptoms and stress burden among caregivers of patients with severe mental illness." European Psychiatry 64, S1 (2021): S126. http://dx.doi.org/10.1192/j.eurpsy.2021.353.

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IntroductionCare givers of patients with severe mental disorders have been shown to be under heavy stress burden that reflect itself through various heterogenous psychiatric symptoms that may mimic PTSD with associated negative impact on interpersonal relations and work performanceObjectivesto assess the prevalence of PTSD symptoms among care givers of patients with severe mental illnessMethods70 patients care givers of sevely mentally ill patients compred to control 70 care giver of patients with chronic debilitating medical illness were recruited from outpatient of the university hospital ou

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van der Plas, Annicka GM, Anneke L. Francke, Luc Deliens, Wim JJ Jansen, Kris C. Vissers, and Bregje D. Onwuteaka-Philipsen. "Informal care givers' experiences with support in primary palliative care when a case manager is involved: A descriptive study in the Netherlands." International Journal of Care Coordination 20, no. 1-2 (2016): 17–25. http://dx.doi.org/10.1177/2053434516685738.

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Introduction Case managers have been introduced in primary palliative care in the Netherlands; these are nurses with expertise in palliative care who offer support to patients and informal care givers. The case manager provides support in addition to the care provided by the home care nurse and general practitioner, potentially leading to more complexities in care coordination. This study describes what informal care givers think about the number of professionals involved in primary palliative care and what support is and is not provided by the general practitioner, the community nurse and the

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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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Hanna, Gay, Pamela Saunders, and Marie Bernard. "Why Creativity Matters to Aging and Health." Innovation in Aging 4, Supplement_1 (2020): 643. http://dx.doi.org/10.1093/geroni/igaa057.2208.

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Abstract As GSA turns 75, it is an appropriate time to review the history of the creative aging movement. This symposium explores the research, policy and practice of creative aging - past and present, starting in the 1970’s through the efforts of pioneering leaders in the aging, humanities and arts in conjunction with growing support from the newly established National Endowment for the Arts and related aging and health service systems. The foundational research by Gene Cohen, MD PHD and others at the turn of the 21st Century will be described in terms of its building the science to utilize t

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&NA;. "POETRY BY CANCER CARE GIVERS." Oncology Times 26, no. 24 (2004): 37. http://dx.doi.org/10.1097/01.cot.0000292727.04215.0a.

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Raskin, Curtis A. "Dermatologists as primary care givers." Journal of the American Academy of Dermatology 37, no. 4 (1997): 668–69. http://dx.doi.org/10.1016/s0190-9622(97)70200-7.

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Mayer, Gloria Gilbert. "Families as Hospital Care Givers." JONA: The Journal of Nursing Administration 31, no. 10 (2001): 457–58. http://dx.doi.org/10.1097/00005110-200110000-00002.

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Dalmer, Nicole K. "‘Add info and stir’: an institutional ethnographic scoping review of family care-givers’ information work." Ageing and Society 40, no. 3 (2018): 663–89. http://dx.doi.org/10.1017/s0144686x18001125.

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AbstractFamily care-givers are increasingly expected to find, understand and use information to meet the complex needs of older adults in their care. A significant number of studies, however, continue to report that care-givers’ information needs are unmet. Following Arksey and O'Malley's scoping review framework, I examined 72 articles for the range and extent of available research on the information work done by family care-givers of community-dwelling older adults living with dementia. To untangle the complex relationship between information and care, this scoping review maps out (a) the wa

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TSUNAKA, MEGUMI, and JENNY C. C. CHUNG. "Care-givers’ perspectives of occupational engagement of persons with dementia." Ageing and Society 32, no. 4 (2011): 543–60. http://dx.doi.org/10.1017/s0144686x11000365.

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ABSTRACTMeaningful engagement in activity is associated with the maintenance of health and wellbeing, but reduced activity participation is common among persons with dementia. Family care-givers play an important role in engaging their relatives with dementia in activities but little is known about their perception of occupational engagement. This study aimed to examine care-givers’ perception of occupational performance of their relatives from three aspects: person, occupation and environment. Adopting a qualitative methodology, semi-structured and in-depth interviews were conducted with 14 f

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Wu, Heng, and Lyn Holley. "Estimating Risk of Elder Abuse: Intergenerational Communication/Empathy, Census-Based Assessment." Innovation in Aging 4, Supplement_1 (2020): 868. http://dx.doi.org/10.1093/geroni/igaa057.3213.

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Abstract COVID highlights the importance of accurate estimates of the risk of elder abuse to guide prevention. Reliability of data is problematic; reports have issues with consistency of definitions, time periods, and stigma. This paper demonstrates the use of US Census data to estimate risk of elder abuse by mapping generational incongruities between care-givers and care-receivers that invite dissonance (Cohen, 2011). Using the 2014-2018 Nebraska Public Use Microdata and 5-year American Community Survey, this research identifies and profiles personal care aides/nursing aides for institutional

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SMITH-CARRIER, TRACY, THUY-NGA PHAM, SABRINA AKHTAR, GAYLE SEDDON, MARK NOWACZYNSKI, and SAMIR K. SINHA. "‘It’s not just the word care, it’s the meaning of the word…(they) actually care': caregivers’ perceptions of home-based primary care in Toronto, Ontario." Ageing and Society 38, no. 10 (2017): 2019–40. http://dx.doi.org/10.1017/s0144686x1700040x.

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ABSTRACTThe frail and homebound older adult populations currently experience difficulties accessing primary care in the medical office. Given this fundamental access to care problem, and the questionable care quality that arises when navigating a labyrinthine health-care system, these populations have typically been subject to inadequate primary care. To meet their needs better, growing research stresses the importance of providing comprehensive home-based primary care (HBPC), delivered by an inter-professional team of health-care providers. Family care-givers typically provide the majority of

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SZINOVACZ, MAXIMILIANE E., and ADAM DAVEY. "Changes in adult children's participation in parent care." Ageing and Society 33, no. 4 (2012): 667–97. http://dx.doi.org/10.1017/s0144686x12000177.

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ABSTRACTCare-giving research has focused on primary care-givers and relied on cross-sectional data. This approach neglects the dynamic and systemic character of care-giver networks. Our analyses address changes in care-givers and care networks over a two-year period using pooled data from the US Health and Retirement Study, 1992–2000. Based on a matrix of specific adult-child care-givers across two consecutive time-points, we assess changes in any adult-child care-giver and examine the predictors of change. A change in care-giver occurred in about two-fifths of care-giving networks. Ability to

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TOLKACHEVA, NATALIA, MARJOLEIN BROESE VAN GROENOU, ALICE DE BOER, and THEO VAN TILBURG. "The impact of informal care-giving networks on adult children's care-giver burden." Ageing and Society 31, no. 1 (2010): 34–51. http://dx.doi.org/10.1017/s0144686x10000711.

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ABSTRACTPrevious research on the care-giver burden experienced by adult children has typically focused on the adult child and parent dyad. This study uses information on multiple informal care-givers and examines how characteristics of the informal care-giving network affect the adult child's care-giver burden. In 2007, 602 Dutch care-givers who were assisting their older parents reported on parental and personal characteristics, care activities, experienced burden and characteristics of other informal care-givers. A path model was applied to assess the relative impact of the informal care-giv

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