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There are 50976 results for: content related to: Informal carers of older family members: how they manage and what support they receive from respite care

  1. You have full text access to this Open Access content
    Estimating service demand for respite care among informal carers of people with psychological disabilities in Australia

    Australian and New Zealand Journal of Public Health

    Volume 39, Issue 3, June 2015, Pages: 284–292, Meredith Harris, Sandra Diminic, Caroline Marshall, Emily Stockings and Louisa Degenhardt

    Version of Record online : 25 FEB 2015, DOI: 10.1111/1753-6405.12337

  2. ‘Give me a break’– respite care for older carers of mentally ill persons

    Scandinavian Journal of Caring Sciences

    Volume 20, Issue 4, December 2006, Pages: 417–426, Yun-Hee Jeon, Henry Brodaty, Colleen O'Neill and Jon Chesterson

    Version of Record online : 20 NOV 2006, DOI: 10.1111/j.1471-6712.2006.00423.x

  3. Strengthening kinship families: scoping the provision of respite care in Australia

    Child & Family Social Work

    Volume 20, Issue 1, February 2015, Pages: 50–61, Juliette Borenstein, Patricia McNamara and on behalf of the Respite Care Consortium

    Version of Record online : 26 DEC 2012, DOI: 10.1111/cfs.12055

  4. You have free access to this content
    Literature review: use of respite by carers of people with dementia

    Health & Social Care in the Community

    Volume 23, Issue 1, January 2015, Pages: 51–63, Christine Neville, Elizabeth Beattie, Elaine Fielding and Margaret MacAndrew

    Version of Record online : 20 JAN 2014, DOI: 10.1111/hsc.12095

  5. Factors influencing the use and provision of respite care services for older families of people with a severe mental illness

    International Journal of Mental Health Nursing

    Volume 16, Issue 2, April 2007, Pages: 96–107, Yun-Hee Jeon, Lynn Chenoweth and Helen McIntosh

    Version of Record online : 8 MAR 2007, DOI: 10.1111/j.1447-0349.2007.00452.x

  6. Respite care for frail older people and their family carers: concept analysis and user focus group findings of a pan-European nursing research project

    Journal of Advanced Nursing

    Volume 30, Issue 6, December 1999, Pages: 1396–1407, Elizabeth J. Hanson, Josephine Tetley and Amanda Clarke

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1365-2648.1999.01215.x

  7. ‘Time and space’: carers’ views about respite care

    Health & Social Care in the Community

    Volume 8, Issue 1, January 2000, Pages: 50–56, Mark Ashworth and Anna H. Baker

    Version of Record online : 9 OCT 2008, DOI: 10.1046/j.1365-2524.2000.00221.x

  8. The impact of organisational culture on the delivery of person-centred care in services providing respite care and short breaks for people with dementia

    Health & Social Care in the Community

    Volume 19, Issue 4, July 2011, Pages: 438–448, Catherine Kirkley, Claire Bamford, Marie Poole, Hilary Arksey, Julian Hughes and John Bond

    Version of Record online : 4 MAY 2011, DOI: 10.1111/j.1365-2524.2011.00998.x

  9. Use of respite care and coping strategies among Irish families of children with intellectual disabilities

    British Journal of Learning Disabilities

    Volume 35, Issue 1, March 2007, Pages: 62–68, Elaine Mac Donald, Elaine Fitzsimons and Patricia Noonan Walsh

    Version of Record online : 20 OCT 2006, DOI: 10.1111/j.1468-3156.2006.00399.x

  10. You have free access to this content
    A review of the factors associated with the non-use of respite services by carers of people with dementia: implications for policy and practice

    Health & Social Care in the Community

    Volume 22, Issue 1, January 2014, Pages: 1–12, Lyn Phillipson, Sandra C. Jones and Christopher Magee

    Version of Record online : 27 MAR 2013, DOI: 10.1111/hsc.12036

  11. You have free access to this content
    Case management approaches to home support for people with dementia

    Intervention Review

    The Cochrane Library

    Siobhan Reilly, Claudia Miranda-Castillo, Reem Malouf, Juanita Hoe, Sandeep Toot, David Challis and Martin Orrell

    Published Online : 5 JAN 2015, DOI: 10.1002/14651858.CD008345.pub2

  12. A time-sovereignty approach to understanding carers of cancer patients' experiences and support preferences

    European Journal of Cancer Care

    Volume 23, Issue 2, March 2014, Pages: 239–248, R.E. Olson

    Version of Record online : 4 SEP 2013, DOI: 10.1111/ecc.12121

  13. Information-sharing with respite care services for older adults: a qualitative exploration of carers' experiences

    Health & Social Care in the Community

    Volume 25, Issue 4, July 2017, Pages: 1404–1415, Linda C. McSwiggan, Judith Marston, Martin Campbell, Timothy B. Kelly and Thilo Kroll

    Version of Record online : 10 MAR 2017, DOI: 10.1111/hsc.12440

  14. Differences and similarities in monetary benefits for informal care in old and new EU member states

    International Journal of Social Welfare

    Volume 25, Issue 1, January 2016, Pages: 7–17, Monika Riedel and Markus Kraus

    Version of Record online : 28 JAN 2015, DOI: 10.1111/ijsw.12157

  15. Why do families relinquish care? An investigation of the factors that lead to relinquishment into out-of-home respite care

    Journal of Intellectual Disability Research

    Volume 55, Issue 4, April 2011, Pages: 422–433, K. Nankervis, A. Rosewarne and M. Vassos

    Version of Record online : 15 FEB 2011, DOI: 10.1111/j.1365-2788.2011.01389.x

  16. You have free access to this content
    The Impacts of short break provision on families with a disabled child: an international literature review

    Health & Social Care in the Community

    Volume 19, Issue 4, July 2011, Pages: 337–371, Janet Robertson, Chris Hatton, Emma Wells, Michelle Collins, Susanne Langer, Vicki Welch and Eric Emerson

    Version of Record online : 22 DEC 2010, DOI: 10.1111/j.1365-2524.2010.00977.x

  17. Rethinking Respite Policy for People With Intellectual and Developmental Disabilities

    Journal of Policy and Practice in Intellectual Disabilities

    Volume 9, Issue 2, June 2012, Pages: 120–126, Jeffrey Chan, Brian Merriman, Trevor Parmenter and Roger Stancliffe

    Version of Record online : 5 JUN 2012, DOI: 10.1111/j.1741-1130.2012.00332.x

  18. Choice in the context of informal care-giving

    Health & Social Care in the Community

    Volume 15, Issue 2, March 2007, Pages: 165–175, Hilary Arksey and Caroline Glendinning

    Version of Record online : 31 OCT 2006, DOI: 10.1111/j.1365-2524.2006.00671.x

  19. Needs of carers of severely disabled people: are they identified and met adequately?

    Health & Social Care in the Community

    Volume 9, Issue 4, July 2001, Pages: 235–243, Paula Kersten, Lindsay McLellan, Steve George, Mark A. Mullee and Jenifer A. E. Smith

    Version of Record online : 21 DEC 2001, DOI: 10.1046/j.1365-2524.2001.00297.x

  20. Home-based palliative care in Sydney, Australia: the carer's perspective on the provision of informal care

    Health & Social Care in the Community

    Volume 15, Issue 2, March 2007, Pages: 97–107, Siggi Zapart, Patricia Kenny, Jane Hall, Betty Servis and Sharon Wiley

    Version of Record online : 9 NOV 2006, DOI: 10.1111/j.1365-2524.2006.00665.x