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Showing 16 to 30 of 43 results Save | Export
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Stein, Gary L.; Sherman, Patricia A.; Bullock, Karen – Educational Gerontology, 2009
An educational program was developed to train practitioners to provide care for patients and families that are responsive to cultural concerns. The aim was to increase knowledge and improve attitudes toward providing culturally proficient and culturally sensitive care for patients and families facing life-threatening illnesses. The program…
Descriptors: Nursing Education, Patients, Program Effectiveness, Program Evaluation
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Csikai, Ellen L.; Herrin, Charlotte; Tang, Maggie; Church, Wesley T., II – Child Welfare, 2008
A mailed survey of child welfare workers in one southern state assessed various aspects of encounters with end-of-life situations in practice. Findings revealed that child deaths, children with life-threatening or life-limiting illnesses, and parental deaths were most commonly encountered and that coworkers were relied on for support. Many had no…
Descriptors: Child Abuse, Child Welfare, Welfare Services, Caseworkers
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Munn, Jean C.; Dobbs, Debra; Meier, Andrea; Williams, Christianna S.; Biola, Holly; Zimmerman, Sheryl – Gerontologist, 2008
Purpose: We designed this study to examine the end-of-life (EOL) experience in long-term care (LTC) based on input from key stakeholders. Design and Methods: The study consisted of 10 homogeneous focus groups drawn from a purposive sample of LTC residents (2 groups; total n = 11), family caregivers (2 groups; total n = 19), paraprofessional staff…
Descriptors: Grounded Theory, Proximity, Residential Care, Hospices (Terminal Care)
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Wilson, Donna M.; Birch, Stephen; Sheps, Sam; Thomas, Roger; Justice, Christopher; MacLeod, Rod – Canadian Journal on Aging, 2008
The vast majority of the 220,000 Canadians who die each year, principally of old age and progressive ill health, do not have access to specialized hospice or palliative care. Hospice and palliative care programs are unevenly distributed across Canada, with existing programs limited in capacity and services varying considerably across programs.…
Descriptors: Hospices (Terminal Care), Terminal Illness, Older Adults, Foreign Countries
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Washington, Karla T.; Bickel-Swenson, Denise; Stephens, Nathan – Health & Social Work, 2008
The present review was undertaken to explore recent evidence in the professional literature pertaining to use of hospice services by African Americans. The article addresses the research methods that have been used to study African American hospice use, obstacles to African American participation in hospice that have been identified, and…
Descriptors: Hospices (Terminal Care), African Americans, African American Community, Research Methodology
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Csikai, Ellen L. – Health and Social Work, 2004
Ethical dilemmas are inherent in every health care setting. A sample of hospice social workers with no direct access to a hospice ethics committee (N = 110) was surveyed regarding ethical issues in hospice care, how the issues were managed, and the extent to which social workers participated in resolution of ethical dilemmas. Common issues…
Descriptors: Patients, Terminal Illness, Social Work, Hospices (Terminal Care)
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Hayslip, Bert, Jr.; And Others – Omega: Journal of Death and Dying, 1991
Analyzed response bias among 34 recipients of care in hospice. Found nonrespondents to have better bereavement prognoses and tended to care for patients who were younger, male, and in program for shorter time. Nonrespondents were in contact with staff less than were respondents. Data are consistent with earlier research showing significant…
Descriptors: Caregivers, Death, Hospices (Terminal Care), Participant Characteristics
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Hodges, Diane – Journal of Poetry Therapy, 1993
Describes a program that used art and poetry therapy with terminally ill patients. Presents the creative writings of two patients. (SR)
Descriptors: Art Therapy, Creative Writing, Hospices (Terminal Care), Poetry
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Death Studies, 1993
Notes that International Work Group on Death, Dying, and Bereavement recognizes wide variation of attitudes, beliefs, and behaviors pertaining to childhood death, dying, and bereavement. Statement identifies set of assumptions which can serve as guidelines, across cultures, in care of children with terminal illness and their families. (Author/NB)
Descriptors: Bereavement, Children, Death, Foreign Countries
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Becker, Janet E. – Health and Social Work, 2004
Members of the Association of Oncology Social Workers completed a survey, which included the Hospice Philosophy Scale (HPS) assessing the likelihood of the worker referring a terminally ill patient to hospice, background and experience, and demographics. The respondents held overwhelmingly favorable attitudes toward hospice philosophy and care,…
Descriptors: Patients, Social Work, Referral, Oncology
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Miller, Pamela J.; Mike, Paula B. – Death Studies, 1995
The political and social development of the Medicare Hospice Benefit combines humanitarian and cost-saving strategies. Although it mainstreamed care of the terminally ill and provided multiple services, four major constraints of the benefit package are identified and explored. It is important that we analyze this policy before we devise new ways…
Descriptors: Death, Federal Aid, Hospices (Terminal Care), Medical Care Evaluation
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Mesler, Mark A. – Omega: Journal of Death and Dying, 1995
Based on nearly three years of participant-observation research in hospice settings, factors that interfere with the hospice philosophy of providing patient autonomy include efforts at symptom control, patient residence, patient disease state, and staff limit setting. Discusses examples, implications, and staff attempts at solutions. (JPS)
Descriptors: Case Studies, Death, Ethics, Higher Education
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Lafer, Barbara – Omega: Journal of Death and Dying, 1991
Reviews findings regarding attrition of hospice volunteers. Suggests ways to improve retention relating to several aspects of volunteer administrator's job including selection of volunteers, training, overseeing transition from training to actual volunteering, structuring communication between volunteers and paid staff, and supervising and…
Descriptors: Communication Skills, Death, Hospices (Terminal Care), Interpersonal Relationship
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Viney, Linda L.; And Others – Journal of Consulting and Clinical Psychology, 1994
Compared quality of life of terminal cancer patients (n=182) in two palliative care units with that of those in general hospital. Patients in specialized palliative care units were found to differ from those dying in hospital, showing less indirectly expressed anger but more positive feelings. They also reported more anxiety about death but less…
Descriptors: Cancer, Death, Foreign Countries, Hospices (Terminal Care)
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Kastenbaum, Robert – Omega: Journal of Death and Dying, 1993
Presents interview with Dame Cicely Saunders, founder of international hospice care movement. Saunders describes her background and experiences that led her to form the hospice movement and discusses the need for pain control for terminally ill patients. Saunders also notes her opposition to euthanasia and physician-assisted suicide. (NB)
Descriptors: Cancer, Death, Helping Relationship, Hospices (Terminal Care)
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