Advanced search
Publication Cover
Progress in Palliative Care
Science and the Art of Caring
Volume 8, 2000 - Issue 6
Submit an article Journal homepage
57
Views
17
CrossRef citations to date
0
Altmetric
Reviews

Communication and Information Needs of Care-Givers of Adult Family Members at Diagnosis and during Treatment of Terminal Cancer

C Grbich
,
D Parker
&
I MaddocksCorrespondence[email protected]
Pages 345-350 | Published online: 13 Jul 2016

Citations (17)

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 (1)

Ian Maddocks. (2000) Sharing the Burden of Care. Progress in Palliative Care 8:6, pages 343-344.
Read now

Articles from other publishers (16)

Anna C. Bibby, Anna J. Morley, Emma Keenan, Nick A. Maskell & Rachael Gooberman-Hill. (2022) The priorities of people with mesothelioma and their carers: A qualitative interview study of trial participation and treatment decisions. European Journal of Oncology Nursing 57, pages 102111.
Crossref
Leonard L. Berry, Shraddha Mahesh Dalwadi & Joseph O. Jacobson. (2017) Supporting the Supporters: What Family Caregivers Need to Care for a Loved One With Cancer. Journal of Oncology Practice 13:1, pages 35-41.
Crossref
Peter L. HudsonElizabeth A. LobbKristina ThomasRachel D. ZordanTom TrauerKaren QuinnAnne WilliamsMichael Summers. (2012) Psycho-Educational Group Intervention for Family Caregivers of Hospitalized Palliative Care Patients: Pilot Study. Journal of Palliative Medicine 15:3, pages 277-281.
Crossref
Una Stenberg, Cornelia M. Ruland & Christine Miaskowski. (2009) Review of the literature on the effects of caring for a patient with cancer. Psycho-Oncology 19:10, pages 1013-1025.
Crossref
Takuya ShinjoTatsuya MoritaKei HiraiMitsunori MiyashitaKazuki SatoSatoru TsunetoYasuo Shima. (2010) Care for Imminently Dying Cancer Patients: Family Members' Experiences and Recommendations. Journal of Clinical Oncology 28:1, pages 142-148.
Crossref
Josephine Clayton & Martin Tattersall. 2009. Textbook of Palliative Medicine. Textbook of Palliative Medicine 1011 1018 .
Josephine M. Clayton, Phyllis N. Butow & Martin H.N. Tattersall. 2009. Palliative Medicine. Palliative Medicine 620 625 .
Josephine M. Clayton, Karen Hancock, Sharon Parker, Phyllis N. Butow, Sharon Walder, Sue Carrick, David Currow, Davina Ghersi, Paul Glare, Rebecca Hagerty, Ian N. Olver & Martin H. N. Tattersall. (2007) Sustaining hope when communicating with terminally ill patients and their families: a systematic review. Psycho-Oncology 17:7, pages 641-659.
Crossref
P Hudson, K Quinn, L Kristjanson, T Thomas, M Braithwaite, J Fisher & M Cockayne. (2008) Evaluation of a psycho-educational group programme for family caregivers in home-based palliative care. Palliative Medicine 22:3, pages 270-280.
Crossref
Karen Hancock, Josephine M Clayton, Sharon M Parker, Sharon Wal der, Phyllis N Butow, Sue Carrick, David Currow, Davina Ghersi, Paul Glare, Rebecca Hagerty & Martin HN Tattersall. (2016) Truth-telling in discussing prognosis in advanced life-limiting illnesses: a systematic review. Palliative Medicine 21:6, pages 507-517.
Crossref
Karen Hancock, Josephine M. Clayton, Sharon M. Parker, Sharon Walder, Phyllis N. Butow, Sue Carrick, David Currow, Davina Ghersi, Paul Glare, Rebecca Hagerty & Martin H.N. Tattersall. (2007) Discrepant Perceptions About End-of-Life Communication: A Systematic Review. Journal of Pain and Symptom Management 34:2, pages 190-200.
Crossref
Sharon M. Parker, Josephine M. Clayton, Karen Hancock, Sharon Walder, Phyllis N. Butow, Sue Carrick, David Currow, Davina Ghersi, Paul Glare, Rebecca Hagerty & Martin H.N. Tattersall. (2007) A Systematic Review of Prognostic/End-of-Life Communication with Adults in the Advanced Stages of a Life-Limiting Illness: Patient/Caregiver Preferences for the Content, Style, and Timing of Information. Journal of Pain and Symptom Management 34:1, pages 81-93.
Crossref
Josephine M Clayton, Karen M Hancock, Phyllis N Butow, Martin H N Tattersall & David C Currow. (2007) Clinical practice guidelines for communicating prognosis and end‐of‐life issues with adults in the advanced stages of a life‐limiting illness, and their caregivers. Medical Journal of Australia 186:S12.
Crossref
Josephine M. Clayton, Phyllis N. Butow & Martin H. N. Tattersall. (2005) The needs of terminally ill cancer patients versus those of caregivers for information regarding prognosis and end-of-life issues. Cancer 103:9, pages 1957-1964.
Crossref
Peter L. Hudson, Sanchia Aranda & Linda J. Kristjanson. (2004) Meeting the Supportive Needs of Family Caregivers in Palliative Care: Challenges for Health Professionals. Journal of Palliative Medicine 7:1, pages 19-25.
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

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.