Supporting lay carers in end of life care: current gaps and future priorities.
about
Interventions for supporting informal caregivers of patients in the terminal phase of a diseaseHow can we help family carers manage pain medicines for patients with advanced cancer? A systematic review of intervention studies.Variances in family carers' quality of life based on selected relationship and caregiving indicators: A quantitative secondary analysis.Protocol for a randomised controlled trial of an outreach support program for family carers of older people discharged from hospital.Factors associated with feelings of reward during ongoing family palliative caregiving.Preparing for family caregiving in specialized palliative home care: an ongoing process.The Melbourne Family Support Program: evidence-based strategies that prepare family caregivers for supporting palliative care patients.Communicating advanced cancer patients' symptoms via the Internet: a pooled analysis of two randomized trials examining caregiver preparedness, physical burden, and negative mood.Effects of a support group programme for patients with life-threatening illness during ongoing palliative care.An examination of the research priorities for a hospice service in New Zealand: A Delphi study.Protocol for a longitudinal qualitative interview study: maintaining psychological well-being in advanced cancer--what can we learn from patients' and carers' own coping strategies?Dying, death and bereavement: a qualitative study of the views of carers of people with heart failure in the UK.A systematic review of psychosocial interventions for family carers of palliative care patients."Ensure that you are well aware of the risks you are taking…": actions and activities medical tourists' informal caregivers can undertake to protect their health and safety.The practice of palliative care from the perspective of patients and carers.PalliPA: How can general practices support caregivers of patients at their end of life in a home-care setting? A study protocolThe perspectives of bereaved family carers on dying at home: the study protocol of 'unpacking the home: family carers' reflections on dying at homeDying at home: a qualitative study of family carers' views of support provided by GPs community staff.The effect of caregiving on bereavement outcome: study protocol for a longitudinal, prospective study.The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial.Family carers providing support to a person dying in the home setting: A narrative literature review.Evaluating the effects of mindfulness-based interventions for informal palliative caregivers: A systematic literature review.Exploring the Support Needs of Family Caregivers of Patients with Brain Cancer Using the CSNAT: A Comparative Study with Other Cancer Groups.Impact of a hospice rapid response service on preferred place of death, and costsFamily Caregivers Who Would Be Unwilling to Provide Care at the End of Life Again: Findings from the Health Survey for England Population Survey.Guidelines for the psychosocial and bereavement support of family caregivers of palliative care patients.Coaching in self-efficacy improves care responses, health and well-being in dementia carers: a pre/post-test/follow-up studyCoping Well with Advanced Cancer: A Serial Qualitative Interview Study with Patients and Family CarersHospice experiences and approaches to support and assess family caregivers in managing medications for home hospice patients: a providers surveyInformal caregiving of hospice patients.A model of caregiving through the end of life: seeking normal.Dying with motor neurone disease, what can we learn from family caregivers?What does respite care mean for palliative care service users and carers? Messages from a conceptual mapping.Evaluating psycho-educational interventions for informal carers of patients receiving cancer care or palliative care: strengths and limitations of different study designs.Perceived risks around choice and decision making at end-of-life: a literature review.A qualitative study exploring the experience of the partners of cancer survivors and their views on the role of primary care.A 10-year literature review of family caregiving for motor neurone disease: moving from caregiver burden studies to palliative care interventions.Carer assessment: continuing tensions and dilemmas for social care practice.The end of life and the family: hospice patients' views on dying as relational."It Has Changed My Life": An Exploration of Caregiver Experiences in Serious Illness.
P2860
Q24236279-1BCEDAEB-F775-479D-8244-5DD3AED0D675Q27318542-F1DB5C35-16AA-4BE9-A8DB-DC60DE3E7ED7Q30151606-19C9F583-BAA8-40B0-97A1-D65BCBBFA1AAQ30203271-58BB32D5-34FE-43A6-BEDB-55B5A41A9625Q30203678-E88DC27E-6C48-4C52-8C86-E8A4230951DEQ30209805-7656EE2C-33C2-4FDB-A9E4-26D4D2CD3CD7Q30217071-C02C0FB4-33C8-4783-B59A-5FB1748840C4Q30224051-2EA3B05C-3633-4F34-9655-29D1D73A5909Q30224633-564673E5-4F34-4778-91CD-7963A3FF27E3Q30375721-B5CEA982-879E-46D1-8A24-CB6B0A19E199Q30540918-D194B6EC-9CB7-4827-B2A2-47FA02F1003EQ33468677-9DFB1E49-8CDE-40D9-B0C7-EF3680A01E7BQ33650436-F88B9444-9943-480D-B64D-7F63C28DA311Q33716662-426C86EA-E022-47BC-BE0A-5DF62B71CAB7Q34092475-B6C9A493-81C6-4C8A-9280-42BCF2D255CFQ34268231-5DCBE4B1-4F00-4D7C-BFB9-1210F54EDEB0Q34486112-674FE6F9-BB15-4BA0-970C-CF01D16E3917Q34555234-7129F7DD-5527-45DA-8590-86D8B4F90A56Q35201145-D0380837-2C09-4ECE-B1F1-7CF8C37D47A0Q35303317-5F4B7D11-06B2-4BBE-84D0-FA86DACAD6EDQ35620622-67D9D4C1-D8FF-4B65-BEBA-2895F46A32B7Q35748009-009719AE-C258-4D41-91F5-83256F75C943Q35872150-3AA2F0D6-CCEF-471F-B1CF-E29F9B9F1769Q35877940-1DB65AF5-3CFA-4086-8C92-FFE72D3510C4Q35904029-94A49464-572E-420D-8D29-75B0958C5FA7Q35996922-20D7707E-CD07-4DD0-8C4A-0EEDEBA5FCB4Q36008630-FFE240B1-5C30-4DB4-9207-931B6D421314Q36255325-779B01B5-4E57-47ED-8E0F-850CF5CFC329Q36711463-78B7572F-8AB8-4EBD-8D9D-45B6DB94C6CBQ36830231-2D736468-78C2-458E-9AD6-BFF7E9A7985DQ37102923-BCB31355-99E7-4BC2-9712-45D49B061945Q37333169-109CD5B4-29F7-4D95-B498-78513397C408Q37790251-04DCD259-5260-4893-8E1D-CCA2B6A29705Q37828011-5FC3FC51-8C84-4460-88C5-2123B445DA25Q37945082-F219D45C-DAB8-4900-9991-E943F7B5E07FQ37987073-31268BEE-14C5-4C66-8D32-14F64F4B4C47Q38036201-4D39DB61-D15E-461F-80E7-DD0BBB52580BQ38253085-CA80F1E0-7EE3-46E1-80AA-53D038EE6D8CQ38496365-CA99725C-FAE1-4C3D-A838-410C17A054F8Q38557857-CE3A2F11-B32E-45C6-B402-E589B101F05F
P2860
Supporting lay carers in end of life care: current gaps and future priorities.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 20 March 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Supporting lay carers in end of life care: current gaps and future priorities.
@en
Supporting lay carers in end of life care: current gaps and future priorities.
@nl
type
label
Supporting lay carers in end of life care: current gaps and future priorities.
@en
Supporting lay carers in end of life care: current gaps and future priorities.
@nl
prefLabel
Supporting lay carers in end of life care: current gaps and future priorities.
@en
Supporting lay carers in end of life care: current gaps and future priorities.
@nl
P2860
P50
P356
P1433
P1476
Supporting lay carers in end of life care: current gaps and future priorities
@en
P2093
J Addington-Hall
P2860
P304
P356
10.1177/0269216309104875
P577
2009-03-20T00:00:00Z