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Councill, Tracy Dee; Ramsey, Kristin – Art Therapy: Journal of the American Art Therapy Association, 2019
This viewpoint describes the case of a 4-year-old boy's journey in art therapy after his cancer had returned, which despite surgery, radiation, and chemotherapy, ultimately claimed his life. The patient and his family participated in art therapy over the course of 18 months. As an integrated, palliative component of treatment, art therapy helped…
Descriptors: Art Therapy, Health Services, Terminal Illness, Cancer
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Pollens, Robin – Topics in Language Disorders, 2020
The client's ability to communicate is key to providing quality palliative end-of-life care. A speech-language pathologist (SLP) can facilitate the patient's ability to communicate concerns or preferences in order to (1) improve the health care team's ability to manage symptoms and engage in end-of-life discussions, and (2) support the patient and…
Descriptors: Terminal Illness, Speech Language Pathology, Allied Health Personnel, Speech Communication
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Sodowsky, Karen – Qualitative Report, 2012
This article is taken from a larger longitudinal study that used caregiver interviews, caregiver surveys, and caregiver statistical information of one community. The interviews were conducted with six spousal caregivers to examine the narratives produced by spouses actively caring for their partners with dementia. The spousal caregivers were…
Descriptors: Dementia, Caregivers, Spouses, Caring
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Temkin-Greener, Helena; Zheng, Nan Tracy; Mukamel, Dana B. – Gerontologist, 2012
Purpose of the study: This study examines urban-rural differences in end-of-life (EOL) quality of care provided to nursing home (NH) residents. Data and Methods: We constructed 3 risk-adjusted EOL quality measures (QMs) for long-term decedent residents: in-hospital death, hospice referral before death, and presence of severe pain. We used…
Descriptors: Hospices (Terminal Care), Community Characteristics, Municipalities, Hospitals
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Heyman, Janna C.; Sealy, Yvette M. – Educational Gerontology, 2011
This study examined physicians' attitude, involvement, and perceived barriers with the health care proxy. A cross sectional, correlational design was used to survey practicing physicians (N = 70). Physicians had positive attitudes toward the health care proxy and indicated that the most significant barriers to health care proxy completion were…
Descriptors: Physicians, Terminal Illness, Health Services, Decision Making
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Jacobsen, Juliet C.; Zhang, Baohui; Block, Susan D.; Maciejewski, Paul K.; Prigerson, Holly G. – Death Studies, 2010
Several studies have shown that the symptoms of grief are different from symptoms of depression among bereaved family members. This study is an attempt to replicate this finding among advanced cancer patients and examine clinical correlates of patient grief and depression. Analyses were conducted on data from interviews with 123 advanced cancer…
Descriptors: Mental Health, Coping, Religion, Health Services
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Patrizi, Patricia A. – New Directions for Evaluation, 2010
The author discusses an assessment of the Robert Wood Johnson Foundation's work over a 20-year period to improve end-of-life care in America. The case illustrates the evolution of the strategy from one focused on a multiyear randomized control trial of a series of hospital-based interventions that produced findings of "no effects" into several…
Descriptors: Terminal Illness, Health Services, Hospices (Terminal Care), Patients
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Pruchno, Rachel; Cartwright, Francine P.; Wilson-Genderson, Maureen – International Journal of Aging and Human Development, 2009
Knowledge about the ways in which race affects decision-making at the end of life is minimal, yet this information is critical for providing culturally sensitive care at the end of life. Data matching socio-demographic characteristics of 34 black and 34 white patients with end-stage renal disease and their spouses reveal that there are no…
Descriptors: Terminal Illness, Decision Making, Context Effect, Racial Differences
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Bern-Klug, Mercedes – Gerontologist, 2009
Purpose: Almost half of people age 85 and older who die annually in the United States die as nursing home residents, yet because it is not always clear who is close to death, not all residents who might benefit from end-of-life care receive it. The purpose of this study is to develop a framework for organizing social interactions related to…
Descriptors: Ethnography, Nursing Homes, Health Services, Role Theory
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Moorman, Sara M.; Carr, Deborah – Gerontologist, 2008
Purpose: We document the extent to which older adults accurately report their spouses' end-of-life treatment preferences, in the hypothetical scenarios of terminal illness with severe physical pain and terminal illness with severe cognitive impairment. We investigate the extent to which accurate reports, inaccurate reports (i.e., errors of…
Descriptors: Spouses, Terminal Illness, Older Adults, Patients
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Cartwright, Juliana C.; Miller, Lois; Volpin, Miriam – Gerontologist, 2009
Purpose: The purpose of this study was to describe good quality care at the end of life (EOL) for hospice-enrolled residents in assisted living facilities (ALFs). Design and Methods: A qualitative descriptive design was used to obtain detailed descriptions of EOL care provided by ALF medication aides, caregivers, nurses, and hospice nurses in…
Descriptors: Terminal Illness, Interviews, Program Effectiveness, Hospices (Terminal Care)
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Tait, Glendon R.; Hodges, Brian D. – Academic Psychiatry, 2009
Objective: The authors examined psychiatric residents' attitudes, perceived preparedness, experiences, and needs in end-of-life care education. They also examined how residents conceptualized good end-of-life care and dignity. Methods: The authors conducted an electronic survey of 116 psychiatric residents at the University of Toronto. The survey…
Descriptors: Curriculum Development, Death, Patients, Educational Experience
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Temkin-Greener, Helena; Zheng, Nan; Norton, Sally A.; Quill, Timothy; Ladwig, Susan; Veazie, Peter – Gerontologist, 2009
Purpose: The objectives of this study were to develop measures of end-of-life (EOL) care processes in nursing homes and to validate the instrument for measuring them. Design and Methods: A survey of directors of nursing was conducted in 608 eligible nursing homes in New York State. Responses were obtained from 313 (51.5% response rate) facilities.…
Descriptors: Nurses, Construct Validity, Nursing, Quality Control
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Carr, Deborah; Khodyakov, Dmitry – Journal of Health and Social Behavior, 2007
Dying persons are encouraged to name as durable power of attorney for health care (DPAHC) someone who will thus be empowered to make end-of-life treatment decisions for them in the event that they become incapacitated. We use data from the Wisconsin Longitudinal Study to investigate whether and whom older adults designate as their DPAHC. DPAHC…
Descriptors: Terminal Illness, Decision Making, Empowerment, Death