Items by Smith, Paula
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Walker, J., Payne, S., Smith, P. and Jarrett, N., 2007. Psychology for Nurses and the Caring Professions, 3rd ed. Berkshire: Open University Press.
Walker, J., Payne, S., Smith, P. and Jarrett, N., eds., 2007. Psychology for Nursing and the Caring Professions (3rd Ed). Maidenhead, U. K.: Open University Press.
Schofield, P., Smith, P., Clarke, A., Faulkner, M., Ryan, T., Kirshbaum, M., Aveyard, B., Dunham, M., Gell, L., Steel, K. and Keogh, T., 2006. An annotated bibliography for pain relief in the terminal stages of palliative care. University of Sheffield, School of Nursing and Midwifery.
Smith, P. and Skilbeck, J., 2008. Working with Family Caregivers in a palliative care setting. In: Payne, S., Seymour, J. and Ingleton, C., eds. Palliative Care Nursing: Principles and Evidence for Practice. 2nd Ed. Buckingham: Open University Press, pp. 326-346.
Smith, P. C., 2007. Cancer pain in the elderly in palliative care settings. In: P, S., ed. Grasping the Nettle: Managing Pain in the Older Adult. John Wiley Press..
Smith, P. C., Wiles, R., Davey, C. and Ashburn, A., 2007. The role of carer in chronic disease and end of life care. In: Kandel, I., Schofield, P. and Merrick, J., eds. Aging and disability. Research and clinical perspectives. Victoria, BC.: Int Acad Press.
Smith, P. C., 2004. Working with Family Caregivers in a palliative care setting. In: Payne, S., Seymour, J., Ingleton, C. and Buckingham,, eds. Palliative Care Nursing: Principles and Evidence for Practice. Open University Press.
Smith, P. C., 2001. Who is a carer? Experiences of family caregivers in palliative care. In: Payne, S. and Ellis-Hill, C., eds. Chronic and Terminal Illness; New perspectives on caring and carers. Oxford: Oxford University Press.
Turner-Cobb, J., Smith, P., Ramchandani, P., Begen, F. and Padkin, A., 2015. Forthcoming. Psychobiological impact of the ICU experience in relatives of patients : A mixed methods assessment of stress, emotional response, coping and support. Psychology, Health & Medicine
Whale, K., Gillison, F. and Smith, P., 2014. “Are you still on that stupid diet?” Women’s experiences of societal pressure and support regarding weight loss, and attitudes towards health policy intervention. Journal of Health Psychology, 19 (12), pp. 1536-1546.
Draper, A., Day, E., Garrood, E. and Smith, P., 2013. Patients and carers experience of living with a complex neurological and palliative diagnosis. Mortality, 18 (3), pp. 270-289.
Smith, P. C., Osborn, M. and Turner-Cobb, J. M., 2012. The big secret, the big lie : unpreparedness for the experience of recovery. Psycho-Oncology, 21 (Supplement 2), p. 10.
Smith, P., 2009. The family caregivers journey in end of life care: recognising and identifying with the role of carer. International Journal on Disability and Human Development, 8 (1), pp. 67-73.
Schofield, P., Smith, P., Aveyard, B. and Black, C., 2007. Complementary Therapies for Pain Management in Palliative Care. Journal of Community Nursing, 21 (8), pp. 10-16.
Smith, P., Schofield, P., Aveyard, B. and Black, C., 2007. Controversies surrounding the management of pain in patients with terminal cancer. British Journal of Community Nursing, 21, p. 10.
Schofield, P. A., Smith, P. and Aveyard, B., 2007. Developing Annotated Bibliographies for pain management - a tool for education, collaboration and research development. Journal of Orthopaedic Nursing, 11 (3-4), pp. 213-219.
Seymour, J., Payne, S., Reid, D., Sargeant, A., Skilbeck, J. and Smith, P., 2005. Ethical and methodological issues in palliative care studies: the experiences of a research group. Journal of Research in Nursing, 10 (2), pp. 169-188.
Payne, S., Sheldon, F., Jarrett, N., Large, S., Smith, P., Davis, C. L., Turner, P. and George, S., 2002. Differences in understanding of specialist palliative care amongst service providers and commissioners in South London. Palliative Medicine, 16 (5), pp. 395-402.
Birtwistle, J., Payne, S., Smith, P. and Kendrick, T., 2002. The role of the district nurse in bereavement support. Journal of Advanced Nursing, 38 (5), pp. 467-478.
Payne, S., Large, S. and Smith, P., 2001. Palliative care patients' perceptions of written information. Psycho-Oncology, 10 May-Jun (3), p. 272.
Conference or Workshop Items
Turner-Cobb, J. M., Smith, P. C., Ramchandani, P., Begen, F. M. and Padkin, A., 2013. Acute psychobiological impact of the intensive care experience in relatives of patients : a mixed methods feasibility study. In: BPS Division of Health Psychology, 2013-09-11 - 2013-09-13, Brighton.
Turner-Cobb, J. M., Smith, P. C., Ramchandani, P., Begen, F. M. and Padkin, A., 2013. Diurnal cortisol rhythmicity in the intensive care setting : the acute stress experience in relatives of patients. In: International Society of PsychoNeuroEndocrinology (ISPNE), 2013, 2013-08-20 - 2013-08-22, Leiden.
Smith, P. C., Osborn, M. and Turner-Cobb, J. M., 2012. The big secret, the big lie : unpreparedness for the experience of recovery. In: British Psychosocial Oncology Society (BPOS), 2012, 2012-01-19 - 2012-01-20, Leeds.
Smith, P. C., Osborn, M., Chan, L. C. and Turner-Cobb, J. M., 2011. Afterwards....provision of support in the recovery from cancer treatment. In: Cancer Research at Bath (CR@B) Meeting, 2011, 2011-11-09, Bath.