Advanced search
Publication Cover
Journal of Community Health Nursing Volume 8, 1991 - Issue 3
Submit an article Journal homepage
25
Views
21
CrossRef citations to date
0
Altmetric
Original Articles

Self-Perceived Needs of Primary Caregivers of Home-Hospice Clients

Susan D. Decker
&
Eva Young
Pages 147-154 | Published online: 07 Jun 2010

Citations (21)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (5)

AloenL. Townsend, KarenJ. Ishler, BethM. Shapiro, Elizabeth Ford Pitorak & CarolR. Matthews. (2010) Levels, Types, and Predictors of Family Caregiver Strain During Hospice Home Care for an Older Adult. Journal of Social Work in End-of-Life & Palliative Care 6:1-2, pages 51-72.
Read now
Peter Hudson. (2004) A Critical Review of Supportive Interventions for Family Caregivers of Patients with Palliative-Stage Cancer. Journal of Psychosocial Oncology 22:4, pages 77-92.
Read now
Mary Pickett, Frances K. Barg & Mary Pat Lynch. (2000) Development of a Home-Based Family Caregiver Cancer Education Program. The Hospice Journal 15:4, pages 19-40.
Read now
Charlotte B. Johnson, Susan C. Slaninka. (1999) BARRIERS TO ACCESSING HOSPICE SERVICES BEFORE A LATE TERMINAL STAGE. Death Studies 23:3, pages 225-238.
Read now
John Trollor. (1997) A survey of carers in the North West Health District of New South Wales. Australian Social Work 50:1, pages 51-55.
Read now

Articles from other publishers (16)

Maija Reblin, Gary Donaldson, Lee Ellington, Kathi Mooney, Michael Caserta & Dale Lund. (2015) Spouse cancer caregivers’ burden and distress at entry to home hospice. Journal of Social and Personal Relationships 33:5, pages 666-686.
Crossref
Adriana D Ventura, Susan Burney, Joanne Brooker, Jane Fletcher & Lina Ricciardelli. (2013) Home-based palliative care: A systematic literature review of the self-reported unmet needs of patients and carers. Palliative Medicine 28:5, pages 391-402.
Crossref
Jessica EmpeñoNatasha T. J. RamingScott A. IrwinRichard A. NelesenLinda S. Lloyd. (2011) The Hospice Caregiver Support Project: Providing Support to Reduce Caregiver Stress. Journal of Palliative Medicine 14:5, pages 593-597.
Crossref
Carole Ann Skalski, Louisa DiGerolamo & Eileen Gigliotti. (2006) Stressors in five client populations: Neuman systems model-based literature review. Journal of Advanced Nursing 56:1, pages 69-78.
Crossref
Peter L. Hudson, Karla Hayman-White, Sanchia Aranda & Linda J. Kristjanson. (2019) Predicting Family Caregiver Psychosocial Functioning in Palliative Care. Journal of Palliative Care 22:3, pages 133-140.
Crossref
PETER HUDSON. (2003) A conceptual model and key variables for guiding supportive interventions for family caregivers of people receiving palliative care. Palliative and Supportive Care 1:4, pages 353-365.
Crossref
John F Deeken, Kathryn L Taylor, Patricia Mangan, K.Robin Yabroff & Jane M Ingham. (2003) Care for the caregivers: a review of self-report instruments developed to measure the burden, needs, and quality of life of informal caregivers. Journal of Pain and Symptom Management 26:4, pages 922-953.
Crossref
Anita Taylor & Ronald S. Taylor. (1998) Neuropsychologic Aspects of Multiple Sclerosis. Physical Medicine and Rehabilitation Clinics of North America 9:3, pages 643-657.
Crossref
Glynda Kinsella, Brian Cooper, Cliff Picton & Douglas Murtagh. (2019) A Review of the Measurement of Caregiver and Family Burden in Palliative Care. Journal of Palliative Care 14:2, pages 37-45.
Crossref
Lesley Wilkes. (1998) Palliative care nursing research trends from 1987 to 1996. International Journal of Palliative Nursing 4:3, pages 128-134.
Crossref
Andrew E. Scharlach, Lorraine T. Midanik, M.Cecilia Runkle & Krikor Soghikian. (1997) Health Practices of Adults with Elder Care Responsibilities. Preventive Medicine 26:2, pages 155-161.
Crossref
Joan S. Grant & Linda Lindsey Davis. (2016) Living with Loss: The Stroke Family Caregiver. Journal of Family Nursing 3:1, pages 36-56.
Crossref
Peg Krach & Jo A Brooks. (1995) Identifying the Responsibilities & Needs of WORKING ADULTS WHO ARE PRIMARYCAREGIVERS. Journal of Gerontological Nursing 21:10, pages 41-50.
Crossref
T.J. Murray. (1995) The Psychosocial Aspects of Multiple Sclerosis. Neurologic Clinics 13:1, pages 197-223.
Crossref
Janet Nevitt & Jane Eisenhaur. 1995. Caring for the Dying Patient and the Family. Caring for the Dying Patient and the Family 200 207 .
Kaye Herth. (2008) Hope in the family caregiver of terminally ill people. Journal of Advanced Nursing 18:4, pages 538-548.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.