Professor Sheila Payne

Sheila Payne BA(Hons), RN, Dip.N, PhD, C.Psychol
Help the Hospices Chair in Hospice Studies,
Director of the International Observatory on End of Life Care,
Director of the Cancer Experiences Collaborative,
President of the European Association for Palliative Care

Publications

Books

Payne S and Walker J. Psychology for Nurses and the Caring Professions, Open University Press: Buckingham, 1996, 228pp.

Payne S, Horn S and Relf M. Loss and Bereavement, Buckingham, Open University Press: Buckingham, 1999.

Payne S and Ellis-Hill C. (eds) Chronic and Terminal Illness: New perspectives on Caring and Carers. Oxford University Press: Oxford, 2001.

Payne S, Seymour J and Ingleton C. (eds) Palliative Care Nursing: Principles and Evidence for Practice. Buckingham: Open University Press, 2004.

Walker J, Payne S, Smith P and Jarrett N. Psychology for Nurses and the Caring Profession. 2nd Edition McGraw-Hill Press, Maidenhead, 2004.

Seymour J, Witherspoon R, Gott M, Ross H and Payne S. Dying in Older Age: End-of-Life Care, Policy Press, Bristol, 2005

Payne S. Advisor to Max Watson, Caroline Lucas, Andrew Hoy and Ian Back Oxford Handbook of Palliative Care, Oxford University Press, Oxford, 2005.

Sque M and Payne S (eds). Organ and tissue donation: An evidence base for Practice. Open University Press, Maidenhead, 2007.

Addington-Hall J, Bruera, E, Higginson J and Payne S. Research Methods in Palliative Care. Oxford University Press, Oxford, 2007.

Payne S, Froggatt K and Hockley J. Bereavement and Loss, Help the Aged, London, 2007.

Walker J, Payne S, Smith P and Jarrett N. Psychology for Nurses and the Caring Professions 3rd Edition. Open University Press, Maidenhead, 2007.

Payne S, Froggatt K. Bereavement. Help the Aged. London (in press).

Payne S, Seymour J and Ingleton C (ed). Palliative Care Nursing: Principles and Evidence for Practice. 2nd edition McGraw-Hill Press: Maidenhead (in press).

Hudson P and Payne S (ed). Family Caregivers and Palliative Care Oxford University Press: Oxford (in preparation).

Book Series

Payne S and Horn S (eds). Health Psychology Book Series, formerly Open University Press: Buckingham now McGraw-Hill Press, Maidenhead.I have commissioned and edited the following books:

· Bennett, P. and Murphy, S. Psychology and Health Promotion, Buckingham, Open University Press, 1997, 184pp.

· Horn, S, and Munafò, M. Pain: Theory, Research and Intervention, Buckingham, Open University Press, 1997, 140pp.

· Bartlett, D. Stress: Perspectives and Processes, Buckingham, Open University Press, 1998, 173pp.

· Hardey, M. The Social Context of Health, Buckingham, Open University Press, 1998, 180pp.

· Payne, S., Horn, S. and Relf, M. Loss and Bereavement, Buckingham, Open University Press, 1999, 138pp.

· Crossley, M. Rethinking Health Psychology, Buckingham, Open University Press, 2000.

· Walker, J. Control and Health Psychology: Theory, Measurement and Applications, Buckingham, Open University Press, 2001

· Lee, C. and Owens, G. The Psychology of Men's Health, Buckingham, Open University Press, 2002

· Berry, D. Risk, Communication and Health Psychology, Buckingham, Open University Press, 2004

· Maclachlan, M. Embodiment, McGraw-Hill Press, Maidenhead, 2004

· Rumsey, N., Harcourt, D. The Psychology of Appearance, McGraw-Hill Press, Maidenhead, 2005

· Berry, D. Health Communication, (in press)

· Newman, S., et al. Self management and Chronic Illness, (in preparation)

· Forshaw, M. Complementary therapy and Health Psychology, (in preparation)

· Stephens, C. Health Promotion and Health Psychology, (in preparation)

· McKee and O'Halon A. Health Psychology and Older People, (in preparation)

Edited Works: Chapter Contributions

Payne S. Models of quality of life. In: Staff Nurse's Survival Guide (2nd ed), London: Austen Cornish, 1992.

Llewelyn S and Payne S. Caring: the costs to nurses and relatives. In: Broome, A. and Llewelyn, S. eds. Health Psychology, Processes and Applications (2nd ed), London: Chapman and Hall, 1994, 109-122.

Farmer A, Payne S and Royle G. A comparative study of psychological morbidity in women with screen detected and symptomatic breast cancer. In: Richardson, A. and Wilson Barnett, J. eds. Nursing Research in Cancer Care, London: Scutari Press, 1995.

Bartlett D and Payne S. Grounded theory - its basis, rationale and procedures. In: McKenzie, G., Powell J and Usher R (eds). Understanding Social Research: Perspectives on Methodology and Practice, London: Falmer Press, 1997, 173-195.

Payne S. Nursing research: a social science? In: McKenzie G, Powell J and Usher R (eds). Understanding Social Research: Perspectives on Methodology and Practice, London: Falmer Press, 1997, 101-111.

Owens G and Payne S. Qualitative approaches to researching death and dying. In: Chamberlain, K. and Murray, M. eds. Qualitative Health Psychology, London: Sage, 1999, 148-163.

Payne S. Interview in qualitative research. In: Memon, A. and Bull, R. eds. Handbook of the Psychology of Interviewing, Chichester, John Wiley, 1999, 89-102.

Feldman L, Payne S and Vivas E. Gender Roles, Role Quality and Health in Venezuelan Working Women: addictive and interactive effects. In: Wamala SP and Lynch Y. eds. Gender and Social Inequalities in Health. Lund, Sweden: Student Literature, 2001.

Payne S and Lloyd-Williams M. Bereavement care. In: M Lloyd-Williams (ed) Psychosocial issues in palliative care. Oxford University Press: Oxford, 2003.

Skilbeck J and Payne S. Palliative Care in Chronic Illness. In: Aranda S and O'Connor M eds. Palliative Care Nursing - a Guide to Practice. 2nd Edition. Victoria, Australia: Ausmed, 2003.

Ballinger C, Yardley L and Payne S. Observation and action research. In: Marks D.F and Yardley L eds. Research Methods for Clinical and Health Psychology. Buckingham: Open University Press, 2004.

Payne S. Designing and conducting qualitative studies. In: Michie S and Abraham C (eds). Health Psychology in Practice. BPS Books, Routledge: London, 2004.

Payne S. Carers and Caregivers. In: Oliviere D and Monroe B (eds). Death, Dying and Social Differences, Oxford University Press: Oxford, 2004, 181-198.

Dean S, Smith J and Payne S. Low back pain: exploring the meaning of exercise management through interpretative phenomenological analysis (IPA). In: L. Finlay and C. Ballinger (eds), Qualitative Research for Allied Health Professionals: Challenging Choices, Whurr Publishers Limited, Chichester, 2006, 10, 139-155.

Payne S. Foreword. In: Schofield, P., Dunham, M., Clarke, A., Faulkner, M., Ryan, T. and Howarth, A. An Annotated Bibliography for the Management of Pain in the Older Adult. University of Sheffield, School of Nursing and Midwifery, 2006.

Payne, S. Survivorship in advanced disease. In: M. Feuerstein (eds), Handbook of Cancer Survivorship. Springer: New York, 2007, 24, 429-446.

Payne S. Resilient carers and caregivers. In: B Monroe and D Oliviere (eds). Resilience in Palliative Care - Achievement in Adversity. Oxford University Press, Oxford, 2007, 5, 83-97.

Payne, S. Grounded Theory. In: Lyons E and Coyle A (eds). Analysing Qualitative Data in Psychology: A practical and comparative guide. London: Sage (in press).

Sque M and Payne S. Report 1: Critical Care Experiences and Bereavement among Families of Organ Donors: A reflective account of grounded theory analysis. In: Lyons E and Coyle A (eds). Analysing Qualitative Data in Psychology: A practical and comparative guide. London: Sage (in press).

Payne S. Palliative care and cancer. In: J. Corner and C. Bailey. Cancer Nursing: Care in Context, (2nd edition), Oxford: Blackwell Science Ltd. (in press).

Payne S. Qualitative Methodology. In: D Walsh et al (eds) Palliatative Medicine 1st Edition. Elsevier: New York (in preparation).

Payne S. and Hudson P. Family Carers In: D Walsh et al (eds) Palliative Medicine 1st Edition. Elsevier: New York (in preparation).

Payne S, Lloyd Williams M and Kennedy V. Bereavement care in M. Lloyd Williams (ed) Psychosocial issues in Palliative Care. 2nd edition. Oxford University Press: Oxford. (in preparation).

Payne S. Bereavement in M. Watson, C. Lucas, A. Hoy and I. Black. Oxford Handbook of Palliative Care. 2nd Edition. Oxford University Press : Oxford (in preparation).

Journal Papers - Academic Journals

Payne S. Anxiety and depression in women with advanced cancer: implications for counselling. Counselling Psychology Quarterly, 1989, 2(3), 337-343.

Payne S. Coping with palliative chemotherapy. Journal of Advanced Nursing, 1990, 15, 652-658.

Payne S. Lay representations of breast cancer. Psychology and Health, 1990, 5, 1-11.

Payne S. A study of quality of life in cancer patients receiving palliative chemotherapy. Social Science and Medicine, 1992, 35(12), 1505-1509.

Bryant A and Payne S. Difficulties inherent in research with cancer patients. Journal of Cancer Care, 1993, 2, 143-146.

Kelvinson R and Payne S. Decision to seek complementary medicine for pain: a controlled study. Complementary Therapies in Medicine, 1993, 1, 2-5.

Payne S. Constraints for nursing in developing a framework for cancer care research. European Journal of Cancer Care, 1993, 2, 117-120.

Smith, L. and Payne, S. A qualitative study of elderly people's perceptions of residential care. Elders, 1993, 2(2), 23-38.

Payne S and Relf M. The assessment of need for bereavement follow-up in palliative and hospice care. Palliative Medicine, 1994, 8, 291-297.

Payne S and Westwell P. Issues for researchers using qualitative methods. Health Psychology Update, 1994, 16, 7-9.

Sque M and Payne S. Gift exchange theory - critique in relation to cadaveric organ transplantation. Journal of Advanced Nursing, 1994, 19, 45-51.

Jarrett N and Payne S A. A selective review of the literature on nurse-patient communication: has the patient's contribution been neglected? Journal of Advanced Nursing, 1995, 22, 72-78.

Low, J T S and Payne S. The good and bad death perceptions of health professionals working in palliative care. European Journal of Cancer Care, 1996, 5, 237-241.

Payne S A, Langley-Evans A and Hillier R. Perceptions of a 'good' death: a comparative study of the views of hospice staff and patients. Palliative Medicine, 1996, 10, 307-312.

Payne S, Hillier R, Langley-Evans A and Roberts T. Impact of witnessing death on hospice patients. Social Science and Medicine, 1996, 43(12), 1785-1794.

Sque M and Payne S A. Dissonant loss: the experience of donor relatives. Social Science and Medicine, 1996, 43(9), 1359-1370.

Langley-Evans A and Payne S. Light-hearted death talk in a palliative day care context. Journal of Advanced Nursing, 1997, 26(6), 1091-1097.

Payne S. Selecting an approach and design in qualitative research. Palliative Medicine, 1997, 11, 249-252.

Payne S. Depression in palliative care patients: a literature review. International Journal of Palliative Nursing, 1998, 4(4), 184-191 (commissioned review paper).

Payne S. To supplant, supplement or support? Organisational issues for hospices. Social Science and Medicine, 1998, 46(11), 1495-1504.

Payne S and Endall M. Detection of anxiety and depression by surgeons and significant others in females attending a breast clinic. European Journal of Oncology Nursing, 1998, 2(1), 4-11.

Payne S, Dean S J and Klaus C. A comparative study of death anxiety in hospice and emergency nurses. Journal of Advanced Nursing, 1998, 28(4), 700-706.

Smith P C and Payne S. Perceptions of family caregivers in palliative care: their role, needs and sources of support. Generations Review, 1998, 8(3), 14.

Fitzsimmons D, George S, Payne S and Johnson C D. Differences in perception of quality of life issues between health professionals and patients with pancreatic cancer. Psycho-Oncology, 1999, 8, 135-143.

Fitzsimmons D, Johnson C D, George S, Payne S, Andrén Sandberg A, Bassi C, Beger H G, BirkD, Büchler M W, Dervenis C, Fernandez Cruz L, Friess H, Grahm A L, Jeekel J, Laugier R, Meyer D, Singer M W and Tihanyi T on behalf of the EORTC Study Group on Quality of Life. Development of a disease specific quality of life (QoL) questionnaire module to supplement the EORTC Core Cancer QoL Questionnaire, the QLQ-C30 in patients with pancreatic cancer. European Journal of Cancer, 1999, 35(6), 939-941.

Jarrett N J, Payne S A and Wiles R A. Terminally ill patients' and lay-carers' perceptions and experiences of community-based services. Journal of Advanced Nursing, 1999, 29(2), 476-483.

Jarrett N, Payne S, Turner P and Hillier R. 'Someone to talk to' and 'pain control': what people expect from a specialist palliative care team. Palliative Medicine, 1999, 13, 139-144.

Low, J.T.S., Payne, S. and Roderick, P. The impact of stroke on informal carers: a literature review. Social Science and Medicine, 49(6), 1999, 711-725.

Payne, S., Smith, P. and Dean S. Identifying the concerns of informal carers in palliative care. Palliative Medicine, 13(1), 1999, 37-44.

Wiles, R., Payne, S. and Jarrett, N. Improving palliative care services: a pragmatic model for evaluating services and assessing unmet need. Palliative Medicine, 13, 1999, 131-137.

Sque, M., Payne, S. and Vlachonikolis I. Cadaveric donotransplantation: nurses' attitudes, knowledge and behaviour. Social Science and Medicine, 1999 50(4) 541-552.

Carrera, C., and Payne, S. Ductal carcinomina in situ (DCIS) of the breast: the need for psycho-social research. Psycho-Oncology, 1999 8:538-545

Jarrett, N.J. and Payne, S.A. Creating and maintaining 'optimism' in cancer care communication. International Journal of Nursing Studies, 2000, 37: 81-90

Payne, S., Powell, J., Hardey, M., Hawker, S. and Kerr, C. Delivering care across professional boundaries: the communication of information about elderly people between health and social care practitioners. Generations Review, 2000, 10(1,: 15-16.

Payne, S., Large, S. and Hawker, S. Elderly patients' perceptions of the readability and content of written information in palliative care. Generations Review, 2000, 10(4): 6-7.

Thompson, F. and Payne, S. Bereaved children's questions to a doctor. Mortality, 2000, 5(1): 74-96.

Payne, S., Large, S., Jarrett, N. and Turner, P. Written information given to patients and families by palliative care units: a national survey. The Lancet, 2000, 355, 1792.

Hardey, M., Payne, S. and Coleman, P. 'Scraps': hidden nursing information and its influence on the delivery of care. Journal of Advanced Nursing, 2000, 32(1), 208-214.

Payne, S., Hardey, M. and Coleman, P. Interactions between nurses during handovers in elderly care. Journal of Advanced Nursing, 2000, 32(2), 277-285.

Ellis-Hill, C., Payne, S. and Ward, C. Self-body split: issues of identity in physical recovery following a stroke. Disability and Rehabilitation, 2000, 22(16), 725-733.

Payne, S., Jarrett, N. and Jeffs, D. The impact of travel on cancer patient's experiences of treatment: a literature review. European Journal of Cancer Care, 2000, 9, 197-203.

Ballinger, C. and Payne, S. Discourse Analysis: Principles, Applications and Critique. British Journal of Occupational Therapy, 2000, 63(12), 566-572.

Ballinger, C. and Payne, S. Falling from Grace or into Expert Hands? Alternative Accounts about Falling in Older People. British Journal of Occupational Therapy, 2000, 63(12), 573-579.

Jones, G.Y. and Payne, S. Searching for safety signals: the experience of medical surveillance amongst men with testicular teratomas. Psycho-Oncology, 2000, 9, 385-395.

Payne, S. The role of volunteers in hospice bereavement support in New Zealand. Palliative Medicine, 2001, 15, 107-115.

Little P, Everitt H, Williamson I, Warne, G, Moore M, Gould C, Ferrier K and Payne S. Preferences of Patients for Patient Centred Approach to Consultation in Primary Care: observational study. British Medical Journal, 2001, (322), 468-472.

May, J., Ellis-Hill, C. and Payne, S. Gatekeeping and Legitimisation: How informal carers' relationship with health care workers is revealed in their everyday interactions. Journal of Advanced Nursing, 2001, 36(3), 364-375.

Payne, S., Jarrett, N., Jeffs, D. and Brown, L. Implications of social isolation during cancer treatment. The implications of residence away from home during cancer treatment on patients' experiences: a comparative study. Health and Place, 2001, 7: 273-282.

Hardey, M., Payne, S., Powell, J., Hawker, S. and Kerr, C. Professional territories and the fragmented landscape of elderly care. The Journal of The Royal Society for the Promotion of Health, 121(3), 2001: 159-164.

Little, P., Everitt, H., Williamson, I., Warner, G., Moore, M., Gould, C., Ferrier, K. and Payne, S. Observational study of patient-centeredness and 'positive' approach on outcomes of general practice consultations. British Medical Journal 2001, 323: 908-911.

Payne, S. Information needs of patients and families. European Journal of Palliative Care, 2002, 9(3): 112-114.

Payne, S., Kerr, C., Hawker, S., Hardey, M. and Powell, J. Delivering care across professional boundaries: the communication of information about older people between health and social care practitioners. Age & Ageing, 2002, 31: 107-117.

Payne, S. Dilemmas in the use of volunteers to provide hospice bereavement support: Evidence from New Zealand. Mortality, 2002, 7(2): 139-154.

Birtwistle, J., Payne, S., Smith, P. and Kendrick, T. The role of the district nurse in bereavement care. Journal of Advanced Nursing, 2002, 38(5): 467-478.

Payne, S., Jarrett, N., Wiles, R. and Field, D. Counselling strategies for bereaved people offered in primary care. Counselling Psychology Quarterly, 2002, 15 (2): 161-177.

Ballinger, C. and Payne, S. The construction of the risk of falling among and by older people. Ageing and Society, 2002, 22 (3): 305-324.

Payne, S. and Haines, R. The contribution of psychologists to specialist palliative care. International Journal of Palliative Nursing, 2002, 8 (8), 401-406.

Lloyd-Williams, M. and Payne, S. Can multi-disciplinary guidelines improve the palliation of symptoms in the terminal phase of dementia? International Journal of Palliative Nursing, 2002, 8 (8), 370-375.

Payne, S., Sheldon, F., Jarrett, N., Large, S., Smith, P., Davis, C., Turner, P. and George, S. Differences in understandings of Specialist Palliative Care amongst service providers and commissioners in South London. Palliative Medicine, 2002, 16:395-402.

Wiles, R., Jarrett, N., Payne, S. and Field, D. Referrals for bereavement counselling in primary care: a qualitative study. Patient Education and Counselling, 2002, 48: 79-85.

Wiles, R., Ashburn, A., Payne, S. and Murphy, C. Patients expectations of recovery following a stroke: a qualitative study. Disability & Rehabilitation 2002, 24 (16): 841-850.

Payne, S. and Haines, R. Doing our bit to ease the pain: the potential contribution of psychology to palliative care. The Psychologist 2002, 15, (11): 564-567.

Hawker, S., Payne, S., Kerr, C., Hardey, M. and Powell, J. Appraising the evidence: reviewing disparate data systematically. Qualitative Health Research, 2002, 12 (9): 1284-1299.

Payne, S. Balancing information needs: dilemmas in producing patient information leaflets. Health Informatics Journal, 2002, (8): 174-179.

Lloyd-Williams, M. and Payne, S. Nurse Specialist Assessment and Management of Palliative Care Patients who are depressed - a Study of Perceptions and Attitudes. Journal of Palliative Care, 2002, 18, (4): 270-274.

Brown, L., Payne, S. and Royle, G. Patient initiated follow-up of breast cancer. Psycho-Oncology, 2002. 11, (4): 346-355.

Lloyd-Williams, M. and Payne, S. A qualitative study of nurses' views on depression in palliative care patients. Palliative Medicine, 2003. 17: 334-338.

Schofield, P. and Payne, S. A pilot study to investigate the potential use of Snoezelen within palliative day care. International Journal of Palliative Nursing, 2003, 9 (3): 124-130.

Wicke, D., Coppin, R. and Payne, S. (2004) Teamworking in nursing homes. Journal of Advanced Nursing 45(2), 197-204.

Rolls, L. and Payne, S. (2003) Childhood Bereavement Services: A survey of UK provision. Palliative Medicine 2003, 17, 423-432.

Skilbeck, J. and Payne, S. Emotional support and the role of Clinical Nurse Specialists in palliative care. Journal of Advanced Nursing 2003, 43(5), 521-530.

Ingleton, C., Payne, S., Nolan, M. and Carey, I. Respite in palliative care: a review and discussion of the literature. Palliative Medicine, 2003, 17 (7), 567-75.

Seymour, J., Ingleton, C., Payne, S. and Beddow, V. Specialist palliative care: patient's experiences. Journal of Advanced Nursing, 2003, 44 (1), 24-33.

Field, D. and Payne, S. Social aspects of bereavement. Cancer Nursing Practice, 2003, 2 (8), 21-25.

Powell, J., Hardey, M., Kerr, C., Hawker, C. and Payne, S. What Counts as Evidence? The Communication of Information about Older People between Health and Social Care Practitioners. Research Policy and Planning, 2003, 21, 1-11.

Little, P., Dorward, M., Gralton, S., Hammerton, L., Pillinger, J., White, P., Moore, M., McKenna, J. and Payne, S. A randomised control trial of three pragmatic approaches to initiate increased physical activity in sedentary patients with risk factors for cardiovascular disease. British Journal of General Practice 2004, 54 (500), 189-95.

Low, J., Roderick, P. and Payne, S. An exploration looking at the impact of domiciliary and day hospital delivery of stroke rehabilitation on informal carers. Clinical Rehabilitation, 2004, 18, 776-784.

Horne, G. and Payne, S. Removing the boundaries: palliative care for patients with heart failure, Palliative Medicine, 2004, 18 (4), 291-296.

Payne, S. Depression in palliative care, Cancer Nursing Practice, 2004, 3 (5), 12-15.

Ashburn, A., Murphy, C., Payne, S. and Wiles, R Discharge from physiotherapy following stroke: the management of disappointment, Social Science & Medicine, 2004, 59 (6), 1263-1273.

Green, A., Payne, S. and Barnitt, R. Illness representations among people with non-epileptic seizures attending a neuropsychiatry clinic: a qualitative study based on the self-regulation model, Seizure, 2004, 13, 331-339.

Ahmed, N., Bestall, J., Ahmedzai, S., Payne, S., Clark, D. and Noble, B. Systematic review of the problems and issues of accessing specialist palliative care by patients, carers and health and social care professionals, Palliative Medicine, 2004, 18 (6), 525-542.

Bestall, J., Ahmed, N., Ahmedzai, S., Payne, S., Noble B. and Clark D. Access and referral to specialist palliative care: patients' and professionals' experiences, International Journal of Palliative Nursing, 2004, 10 (8), 381-389.

Payne, S., Kerr, C., Hawker, S., Seamark, D., Davis, C., Roberts, H., Jarrett, N., Roderick, P. and Smith, H. A Survey of the Provision of Palliative Care in Community Hospitals: an unrecognised resource, Journal of the Royal Society of Medicine, 2004, 97 (9), 428-431.

Payne, S., Ingleton, C., Scott, C., Steele, K. and Nolan, M. A survey of the perspectives of specialist palliative care providers in the UK of in-patient respite, Palliative Medicine, 2004, 18, (8), 692-697.

Payne, S. and Field, D. Undertaking bereavement research: sensitivities and sensibilities. Grief Matters: Australian Journal of Bereavement, 2004, 7 (3), 52-56.

Rolls, L. and Payne, S. Childhood bereavement services: issues in UK service provision. Mortality, 2004, 9 (4), 300-328.

Field, D., Reid, D., Payne, S. and Relf, M. A national postal survey of adult bereavement support in hospice and specialist palliative care services in the UK. International Journal of Palliative Nursing, 2004, 10 (12), 569-576.

Payne, S., Chapman, A., Holloway, M., Seymour, J. and Chau, R. Chinese Community Views: Promoting Cultural Competence in Palliative Care, Journal of Palliative Care, 2005 21 (2), 111-116.

Payne, S. Depression in palliative care. Cancer Nursing Practice, March 2005 supplement, 20-22.

Field, D. and Payne, S. Social aspects of bereavement. Cancer Nursing Practice, March 2005 supplement, 27-29.

Sque, M., Long, T. and Payne, S. Organ Donation: Key Factors Influencing Families' Decision-Making. Transplantation Proceedings, March 2005, 37 (2), 543-546.

Seymour, J., Payne, S., Reid, D., Sargeant, A., Skilbeck, J. and Smith, P. Ethical and methodological issues in palliative care studies: The experiences of a research group. Journal of Research in Nursing, 2005, 10 (2), 169-188.

Dean, S., Smith, J., Payne, S. and Weinman, J. 'Managing Time': An interpretative phenomenological analysis of patients' and physiotherapists': perceptions of adherence to therapeutic exercise for low back pain. Disability and Rehabilitation, 2005, 27 (11), 625-636.

Cheraghi, A., Payne, S. and Salsali, M. Spiritual aspects of end-of-life care for Muslim patients: experiences from Iran. International Journal of Palliative Nursing, 2005, 11 (9), 468-474

Skilbeck, J. and Payne, S. End-of-Life care: a discursive analysis of specialist palliative care nursing, Journal of Advanced Nursing, 2005, 51 (4), 325-334.

Barnes, S., Gott, M., Payne, S., Parker, C., Seamark, D., Gariballa, S. and Small, N. Recruiting older people into a large, community-based study of heart failure. Chronic Illness, 2005, 1, 321-329.

Skilbeck, J., Payne, S., Ingleton, C., Nolan, M., Carey, I. and Hanson, A. An exploration of family carers' experience of respite services in one specialist palliative care unit. Palliative Medicine, 2005, 19, 610-618.

McDermott, E., Bingley, A.F., Thomas, C., Payne, S., Seymour, J. and Clark, D. Viewing patient need through professional writings: a systematic 'ethnographic' review of palliative care professionals' experiences of caring for people with cancer at the end of life. Progress in Palliative Care, 2006, 14 (1), 9-18.

Gott, M., Barnes, S., Parker, C., Payne, S., Seamark, D., Gariballa, S. and Small, N. Predictors of the quality of life of older people with heart failure recruited from primary care. Age and Ageing, 2006, 35 (2), 172-177.

Hughes, P., Noble, B., Payne, S., Ingleton, C. and Parker, C. Evaluating an education programme in general palliative care for community nurses. International Journal of Palliative Nursing, 2006, 12 (3), 123-131.

Kerr, C., Hawker, S., Payne, S., Seamark, D. and Lloyd-Williams, M. Out of hours medical cover in community hospitals: implications for palliative care. International Journal of Palliative Nursing, 2006, 12 (2), 75-80.

Bingley, A. F., McDermott, E., Thomas, C., Payne, S., Seymour, J. E. and Clark, D. Making sense of dying: a review of narratives written since 1950 by people facing death from cancer and other diseases. Palliative Medicine, 2006, 20 (3), 183-195

Sque, S., Payne, S. (Editorial) Current issues in organ donation and transplantation. Mortality Special Issue on organ donation, (we were invited to be the guest editors of a special edition on organ donation). May 2006, 11(2), 111-116.

Sque, S., Payne, S. and Macleod Clark, J. Organ donation: Gift of life or sacrifice. Mortality, May 2006, 11(2), 117-133.

Hudson, P., and Payne, S. An International Collaboration for Family Carer Research. European Journal of Palliative Care, 2006, 13(4), 135.

Froggatt K and Payne S. A survey of end-of-life care in care homes: issues of definition and practice. Health and Social Care in the Community, 2006, 14(4), 341-348.

Hawker S, Kerr C, Payne S, Seamark D, Davis C, Roberts H, Jarrett N, Roderick P and Smith H. End of life care in community hospitals: the perceptions of bereaved family members. Palliative Medicine, 2006, 20: 541-547.

Reid D, Payne S, Field D and Relf, M. Adult bereavement in five English Hospices: participants, organisations and pre-bereavement support. International Journal of Palliative Nursing, 2006, 12(7): 320-327.

Payne S. Commentary on Jocham HR, Dassen T, Widdershoven G and Halfens R (2005) Quality of life in palliative care and cancer patients - a literature review. Journal of Clinical Nursing, September 2006, 15(9), 1188-1195.

Barnes S, Gott M, Payne S, Parker C, Seamark D, Gariballa S and Small N. Characteristics and views of family carers in older people with heart failure. International Journal of Palliative Nursing, 2006, 12(8), 380-389.

Field, D, Reid, D, Payne S and Relf M. Adult bereavement in five English Hospices: types of support. International Journal of Palliative Nursing, 2006, 12(9), 430-437.

Barnes S, Gott M, Payne S, Seamark D, Parker C, Gariballa S and Small N. Prevalence of symptoms in a community-based sample of heart failure patients. Journal of Pain and Symptom Management, 2006, 32(3), 208-216.

Barnes, S., Gott, M., Payne, S., Seamark, D., Parker, C., Gariballa, S. and Small, N. Communication in heart failure: perspectives from older people and primary care professionals. Health and Social Care in the Community, 2006. 14 (6), 482-490.

Bailey, C, Wilson, R, Addington-Hall, J, Payne, S, Williams, M, Molassiotis, A, Seymour, J. The Cancer Experiences Research Collaborative (CECo): building research capacity in supportive and palliative care. Progress in Palliative Care, 2006, 14(6), 265-270.

O'Connor M and Payne S. Discourse analysis; examining the potential for research in palliative care. Palliative Medicine, 2006, 20, 829-834.

Field D, Payne S, Relf M and Reid D. An overview of adult bereavement support in the United Kingdom: Issues for policy and practice. Social Science and Medicine, 2007, 64(2), 428-438.

Gott M, Barnes S, Payne S, Seamark D, Parker C, Gariballa S and Small N. Dying trajectories in heart failure. Palliative Medicine, 2007, 21, 95-99.

Payne S, Field D, Kerr C, Hawker S and Rolls L. Evaluating case study methods research for use in end of life care practice: reflections on three studies. Journal of Advanced Nursing, 2007, 58(3), 236-245.

Payne S. (Editorial) Public health and palliative care. Progress in Palliative Care, 2007, 15(3), 101-102.

Payne S, Hawker S, Kerr C, Seamark D, Jarrett N, Roberts H, Smith H. Health Care Workers Skills, Perceived Competence and Experiences of End of Life Care in Community Hospitals. Progress in Palliative Care, 2007, 15(3), 118-125.

Sargeant A, Payne S, Gott M, Small N, Oliviere D. User involvement in palliative care: Motivational factors for service users and professionals. Progress in Palliative Care, 2007, 15(3), 126-132.

Payne S, Kerr, C, Hawker S, Seamark D, Davis C, Roberts H, Jarrett N and Smith H. Dying in old age in community hospitals in the United Kingdom: perceptions of patients, carers and bereaved carers. Health and Social Care in the Community, 2007, 58(3), 236-245.

Rolls L and Payne S. Children and Young People's Experience of UK Childhood Bereavement Services, Mortality, 2007, 12(3), 281-303.

Stevens T, Payne S A, Burton C, Addington-Hall J and Jones A. Palliative care in stroke: a critical review of the literature. Palliative Medicine, 2007, 21, 323-331.

Gott M, Barnes S, Payne S, Parker C, Seamark D, Gariballa S and Small N. Patient views of Social Services provision for older people with advanced heart failure. Health and Social Care in the Community, 2007, 15(4), 333-342.

Seymour J, Payne S, Chapman A and Holloway M. Hospice or home? Expectations of end-of-life care among white and Chinese older people in the UK. Sociology of Health and Illness, Special Edition on Ethnicity and Health, 2007, 29(6), 872-890.

Dean S, Weinman J and Payne S. Utility of the Orthosense Positive Monitor for facilitating exercise and postural advice for low back pain: a pilot study, Manual Therapy, (in press).

Rolls L and Payne S. What is the contribution of unpaid volunteers to childhood bereavement services? Mortality, (in press)

Barnes S, Gott M, Payne S, Parker C, Seamark D, Gariballa S and Small N. Predicting mortality among a community-based sample of older people with heart failure. Chronic Illness. (in press)

Ellis-Hill, C, Payne S and Ward C. Using stroke to explore 'The Life Thread Model': an alternative approach to rehabilitation. Disability and Rehabilitation, (in press).

Gott M, Barnes S, Payne S, Parker C, Seamark D, Gariballa, S and Small N. (under consideration). Psychosocial support needs of older people with heart failure and their bereaved carers; the role of GP's. European Journal of General Practice. (submitted)

Gott M, Barnes S, Payne S, Parker C, Seamark D, Gariballa S and Small N. (under consideration). Palliative care in heart failure: the need to address co-morbidities. Journal of Palliative Care. (submitted)

Sque M, Long T, Payne S, Roche W and Speck P. The UK post-mortem organ retention crisis of 1999-2004: what it meant to involved families and health professionals. Journal of Advanced Nursing. (submitted).

Gott M, Barnes S, Payne S, Seamark D, Parker C, Gariballa S and Small N. Attitudes to death and dying in heart failure patients. Social Science and Medicine, (in preparation).

Gott M, Barnes S, Payne S, Seamark D, Parker C, Gariballa S and Small N. Educational needs of primary care professionals in palliative care for heart failure. Education for Primary Care, (in preparation).

Reeve J, Lloyd-Williams M, Payne S and Dowrick D. Medicine with sociology: a case study looking at distress in people with terminal cancer from the perspective of a General Practitioner. Sociology of Health and Illness (in preparation).

Kerr C, Hawker S and Payne S. End of Life care for older people and their families in UK community hospitals: the perspectives of clinical managers. End of Life Care (in preparation).

Journal Papers - Professional Journals

Glasper, A., Miller, S. and Payne, S. Coming out. Paediatric Nursing, 1991, 3(4), 5-7.

Payne S. Cancer patients perception of health. Senior Nurse, 1992, 11(2), 29-32.

Payne S. How is life treating you? Professional Nurse, 1991, 6(9), 531-535.

Payne S. and James B. Perceptions of bereavement support. Senior Nurse, 1992, 12(3), 44-45.

Payne S and James B. Can they understand you? Nursing Management, 1995, 2(7), 12‑13.

Payne, S. Research and development: Plans for the School of Occupational Therapy and Physiotherapy, University of Southampton. Southampton Health Journal, 1996, 12(2), 18-19.

Payne, S. South and West Palliative Care Research Network. Information Exchange, December, 1997, 2.

Payne, S. Invited Commentary of Sitzia, J. and Dikken, C. Survey of the incidence and severity of self-effects reported by patients receiving six cycles of FEC chemotherapy, Journal of Cancer Nursing, 2, 1997, 61-73. In: Journal of Cancer Nursing, 1997, 1(2), 74.

Payne, S. Expanding the limits of care: the contribution of health psychology to palliative care. New Zealand Psychology Society Newsletter, 1999, 3:3-4.

Payne, S. (Editorial) Research involves small steps not giant leaps. International Journal of Palliative Nursing, 2000, 6(2): 56.

Payne, S. Invited commentary of Irma PM Kruijver, Ada Kerkstra, Jan J Kerssens, Chantal CM Holtkamp, Jozien M Bensing, Harry BM van de Wiel. Communication between nurses and simulated patients with cancer: evaluation of a communication training programme. European Journal of Oncology Nursing, 2001, 5(3): 152.

Payne, S. (Editorial) Bereavement support: something for everyone? International Journal of Palliative Nursing, 2001, 7(3): 108.

Payne, S., Kerr, C. and Hawker, S. The Provision of Palliative Care for Elderly People in Community Hospitals: Best Hope or Last Hope? 'Challenge' Newsletter of the Community Hospitals Association, 2002: 33, 8.

Payne, S., Kerr, C. and Hawker, S. The Provision of Palliative Care for Elderly People in Community Hospitals: Best Hope or Last Hope? British Psychosocial Oncology Society Newsletter, March 2002: 10-11.

Payne, S. (Editorial) Are we using the users? International Journal of Palliative Nursing, 2002, 8(5): 212.

Sque, M., Long, T. and Payne, S. Research Notes. Nursing Standard, 2003, 17 (34): 21.

Payne, S. Invited commentary. The benefits of involving patients in healthcare planning remain uncertain. Evidence based Health Care, 2003, 7, 83-84.

Payne, S., Field, D., Relf, M. and Reid, D. Evaluating bereavement support provided to older people by hospices. READ (Research Endeavours and Dissemination), School of Nursing & Midwifery, University of Sheffield, Winter 2003.

Reid, D., Payne, S., Field, D. and Relf, M. Evaluating bereavement support to older people by hospices: an update. READ (Research Endeavours and Dissemination), School of Nursing & Midwifery, University of Sheffield, Spring/Summer 2004.

Payne, S. NICE Supportive and Palliative Care Guidance, International Journal of Palliative Nursing, 2004, 10 (3), 123.

Payne, S. and Speck, P. Reflections on the contribution of Frances Sheldon, International Journal of Palliative Nursing, 2004, 10 (4), 202-203.

Payne, S. (Editorial) Conferences: Opportunities for all. International Journal of Palliative Nursing, 2004, 10 (6), 268.

Payne, S., Seymour, J. and Ingleton, C. Response to: Watson R. (2003) 'Editorial', Journal of Advanced Nursing, 2004, 219 -220.

Sargeant, A. and Payne, S. User involvement in Palliative Care: a scoping exercise. READ, 2004, 2, 4-5.

Payne, S. Nursing research: do we still need to be concerned? International Journal of Palliative Nursing, 2005, 11 (3), 106-107.

Lloyd-Williams, M., Payne, S. and Dennis, M. Letter: Specialist palliative care in dementia: Patients with dementia are unable to access appropriate palliative care. British Medical Journal, 2005, (330), 671-672.

Field, D., Reid, D., Payne, S. and Relf, M. Adult bereavement support in five English hospices. Mortality, 2005, 10, 29.

Payne, S. Commentary on Jocham, H.R., Dassen, T., Widdershoven, G. and Halfens, R. Quality of life in palliative care cancer patients: a literature review. Journal of Clinical Nursing, 2005, 14.

Payne, S. Evaluating adult bereavement support services in hospices. Hospice Information bulletin, Nov 2005, 11-12.

Payne S and Froggatt K. Dying in late old age: the final frontier? (editorial) International Journal of Palliative Nursing, (Invited editors to special edition on older people and palliative care). May 2006, 12(5), 200-202.

Sque, M, Long, T Payne, S and Allardyce, D. Organ Donation: gift of life or sacrifice? UK Transplant Bulletin, Summer 2006, 59, 10-11.

Long, T, Sque, M and Payne S. Information Sharing: its impact on donor and nondonor families' experiences in the hospital. Progress in Transplantation, June 2006, 144-149

Sque M, Long T, Payne S and Allardyce D. Organ Donation - Understanding Bereaved Families. Transworld, 2006, Issue 1, 16-17.

Payne S. Research…so what's it all about?. The research page: bringing research to people in Hospices. Hospice Bulletin, November 2006, 5(2), 3.

Payne S. The research page: Supportive and Palliative Care - 'Cancer Experiences'. Hospice Bulletin, 2007, 5(3), 3.

Hudson P and Payne S. Collaboration on research into family carers moves a step forward. European Journal of Palliative Care, 2007, 14(5), 218.

Payne S. Reinforcing our aims: 'Better research by better researchers'. CECo News, June 2007, 1(2), 1.

Official Reports

Payne S and Hillier R. The Impact of Death on Fellow Patients in a Palliative Care Unit, Final Research Report to Wessex Regional Health Authority, 1995, 41pp.

Payne S, Wiles R and Jarrett N. The Support of Palliative Care Patients and Their Carers in the Community, Final Report to Barking, Havering and Brentwood Community Healthcare NHS Trust, 1997, 96pp.

Payne S. Care of the Dying - Access to Hospice Services in the North Island of New Zealand, Final Research Report to The Florence Nightingale Foundation and The General Nursing Council for England and Wales Trust, 1997, 58pp.

Payne S, Turne, P, Hillier R and Jarrett N. Care of the Dying at Home: Access to Multi‑disciplinary Specialist Palliative Care, Final Research Report to the NHS Executive South and West Research and Development Directorate, 1997, 50pp.

Fitzsimmons D, George S, Payne S, Johnson C D. et al. Phase 1-3 Development of a Pancreatic Cancer Quality of Life Module to Supplement the EORTC Core Cancer Quality of Life Module, QLQ-C30, Internal Peer Review Document for the EORTC Quality of Life Study Group, 1997, 120pp.

Payne S. Research strategy. In: School Strategic Plan 1997-2002, School of Occupational Therapy and Physiotherapy, University of Southampton, 1997, 9-11.

Payne S. The Support Needs of Informal Carers of Cancer Patients Receiving Palliative Care. Final Report to the Wessex Medical Trust, 1998, 40pp.

Payne S, Hardey M and Coleman P. Clinical Discourses: Interactions Between Nurses in Elderly Care. Final Report to the NHS Executive South and West, 1998, 32pp.

Payne S, Jarrett N and Ahmad N. Cancer Treatment Far From Home: A Comparative Investigation of Patients' Experiences and the Availability of Social Support - A Literature Review. Commissioned by the States of Guernsey Board of Health, 1998, 33pp.

Payne S, Turner P, Hillier R and Jarrett N. Outcomes of Referral to Specialist Palliative Care Services: The Consumer Perspective. Final Report to the Wessex Medical Trust, 1998, 25pp.

Payne S. Hospice Bereavement Support: The Role of Volunteers. Final Report to the Winston Churchill Memorial Trust, 1999, 31pp.

Wiles R, Payne S, Barnitt R, Wheeler A and Swan R. A Comparison of Different Types of Pre-registration for Occupational Therapists and Physiotherapists and Its Relevance to First Post Performance. Final Report to the Department of Health, 1999, 88pp.

Payne S, Jarrett N, and Brown L. Cancer Treatment Far From Home: A Comparative Investigation of Patients' Experiences and the Availability of Social Support. Final Report to the States of Guernsey Department of Public Health. Southampton: Health Research Unit, School of Health Professions and Rehabilitation Sciences, University of Southampton. 1999 37pp.

Payne S. Research strategy. In: School Strategic Plan 2000-2004, School of Health Professions and Rehabilitation Sciences. University of Southampton, 2000.

Payne S, Jarrett N, and Turner P. The Readability and Content of Written Information Provided to Patients and Families by Palliative Care Units: A National Survey. Final Report to the NHS Executive South East, 2000.

Conroy, MC., Payne, S., Ledger, M. and Blackmore, C. In Transition: From Systematic Review to a Redesigned Occupational Therapy In-Patient Service for Persons Suffering from an Acute Psychiatric Episode. Final Report to NHSE South East, 2000, 1-45.

Wiles, R., Ashburn, A., Payne, S., Murphy, C., and Campbell, F. A study of the information giving process between physiotherapists and patients in relation to recovery following stroke. Final Report to NHSE South East, 2000.

Royle, G., Payne, S., and Brown, L. A study of patient initiated follow-up of breast cancer. Final Report to Astra Zeneca, 2000.

Payne, S., Large, S., Smith, P., and Kubesch, N. Elderly patients' perceptions of the readability and content of written information in palliative care. Final Report to the Averil Osborn Fund, 2000.

Payne, S., Wiles, R., Field, D. and Jarrett, N. Counselling the bereaved in general practice. Final Report to NHSE South East., 2000.

Payne, S., George, S., Davis, C., Sheldon, F., Jarrett, N. and Turner, P. Marie Curie Cancer Care Specialist Palliative Care Project (Caterham) Phase 1. Final Report to Marie Curie Cancer Care, 2000.

Payne, S., Hardey, M. and Powell, J. Delivering care across professional boundaries: the communication of information about elderly people between health and social care practitioners. Final Report to NHSE South East, 2001.

Horne, G. and Payne, S. Removing the Boundaries: Specialist Palliative Care for Heart Failure. Final Report to Health Action Zone (DoH), 2001.

Schofield, P., Payne, S. and Brooks, D. The feasibility of using Snoezelen within a palliative care day setting: a randomised controlled trial investigating the potential. Final report to the Wilkes Fund, Trent Palliative Care Centre, Sheffield, 2001.

Sque, M., Long, T. and Payne, S. Organ and tissue donation: Exploring the needs of families. Final report to the British Organ Donor Society and National Lottery Community Fund, 2003.

Rolls, L. and Payne, S. Helping communities develop a childhood bereavement service. Final Report to the Clara E Burgess Charity 2003.

Payne, S., Kerr, C., Hawker, S., Seamark, D., Davis, C., Roberts, H., Jarrett, N., Roderick, P. and Smith, H. The Provision of Palliative Care for Elderly People in Community Hospitals: best hope or last hope? Final Report to The Health Foundation, 2004.

Seymour, J., Witherspoon, R., Gott, M., Ross, H. and Payne, S. Thinking about the future: promoting comfort, choice and well being for older people at the end of their lives, Help the Aged, 2004.

Payne, S., Ingleton, C., Scott, G., Steele, K., Nolan, M. and Carey, I. A survey of the perspectives of specialist palliative care providers in the UK of in-patient respite, Final Report to the University of Sheffield, 2004.

Hughes, P., Payne, S. and Noble, B. Final Report of an evaluation of the North Trent Cancer Network District Nurse/Community Nurse Education Programme in Palliative Care, Department of Health, 2004.

Sque, M., Long, T. and Payne, S. Families who did not donate organs: Recruiting potential participants. Final report for the British Organ Donor Society and the Community Fund, 2004.

Sque, M., Long, T. and Payne, S. From understanding to implementation: meeting the needs of families and individuals affected by post mortem organ retention. Final Report to the Department of Health and the Retained Organs Commission, 2004.

Ahmedzai, S. H., Payne, S., Bestall, J. C., Ahmed, N., Dobson, K., Clark, D. and Noble, B. Improving Access to Specialist Palliative Care: Developing a screening measure to assess the distress caused by advanced illness that may require referral to specialist palliative care. Final Report to the Elizabeth Clark Charitable Trust, 2005.

Clark, D., Thomas, C., McDermott, E., Bingley, A., Payne, S. and Seymour, J. What are the views of people affected by cancer and other illnesses about end of life issues? Professional and patient perspectives. Final Report to the Macmillan Cancer Relief, 2005.

Payne, S., Gott, M., Small, N., Oliviere, D., Thomas, J., Young, E. and Sargeant, A. User-Involvement in Palliative Care: a scoping study. Final Report to St. Christopher's Hospice, 2005.

Payne, S., Field, D., Relf, M. and Reid, D. Evaluating bereavement support provided to older people by hospices. Final Report to The Health Foundation, 2005.

Field, D., Reid, D., Payne, S. and Relf, M. Adult Bereavement Support in Five Hospices in England. Final Report, 2005.

Payne, S., Seymour, J., Holloway, M. and Chapman, A. Exploring and understanding the views of older Chinese people about cancer and end-of-life care. Final Report, 2005.

Smith P, Payne S and Ramcharan P. Carers of the Terminally Ill and Employment Issues: a comprehensive literature review. Final report for Help the Hospices, January 2006.

Sque, M., Allardyce, D., Long, T. and Payne, S. Exploring the end of life decision-making and hospital experiences of families who did not donate organs or tissues for transplant operations. Final Report for UK Transplant, February 2006.

Skilbeck, J, Davis G, Payne, S and Reid, D. End-of-Life Care for Older People in Rotherham. Final Report for Rotherham NHS Primary Care Trust, September 2006.

Gott, M., Barnes, S., Payne, S., Seamark, D., Parker, C, Gariballa, S and Small, N. A Multi-centre Longitudinal Study to Identify the Palliative Care Needs of Older People with Heart Failure and their Families: Executive Summary. The University of Sheffield, August 2006.

Reviews of Single Academic Books

Payne, S. Review of Eiser, C. Chronic Childhood Disease. In: British Journal of Psychology, 1991, 82(4), 556-557.

Payne, S. Review of Garrison, W.T. and McQuiston, S. Chronic Illness During Childhood and Adolescence: Psychological Aspects. In: British Journal of Psychology, 1991, 82(4), 555-556.

Payne, S. Review of Parry, G. Coping with Crises. In: British Journal of Psychology, 1991, 82(2), 241-242.

Payne, S. Review of Phillips, C., Palfrey C. and Thomas P. Evaluating Health and Social Care. In: Journal of Advanced Nursing, 1994, 19(6), 1257-1258.

Payne, S. Review of Segal, J. and Simkins, J. My Mum Needs Me: Children with Ill or Disabled Parents. In: Health Psychology Update, 1994, 16, 34-35.

Payne S. Review of Digby, Tantam and Max eds. Psychology and the Social Sciences. In: Journal of Advanced Nursing, 1994, 20(3), 578-579.

Payne S. Review of Faulkner, A. Teaching Interactive Skills in Health Care. In: Health Psychology Update, 1994, 17, 45.

Payne S. Review of Niven, N. Health Psychology (2nd edition). In: Journal of Advanced Nursing, 1995, 21(3), 614.

Payne S. Review of Katz, J. and Sidell, M. Easeful Death: Caring for Dying and Bereaved People. In: Palliative Medicine, 1996, 10, 173-174.

Payne S. New journal - new agenda? Review of Journal of Health Psychology 1(1), Sage Publications. In: Health Psychology Update, 1996, 24, 19-21.

Payne S. Review of Burton, M. and Watson, M. eds. Counselling People with Cancer, Chichester, John Wiley, 1998, 197pp. In: Palliative Medicine, 1998, 12, 311-312.

Payne S. Review of Holloway, I. Basic Concepts for Qualitative Research, Oxford, Blackwell Science, 1997, 186pp. In: Journal of Advanced Nursing, 1998, 28(4), 918.

Payne S. Review of Hugman, R., Peelo, M. and Soothill, K. eds. Concepts of Care: Developments in Health and Social Welfare, London, Arnold, 1997, 216pp. In: Journal of Advanced Nursing, 1998, 28(2), 448.

Payne S. Review of Johnson, M. Nursing Power and Social Judgement, Aldershot, Ashgate, 1997, 228pp. In: Journal of Advanced Nursing, 1998, 28(6), 1359.

Payne S. Review of Quinn, S. Uncertain Lives, Untimely Deaths - Experiences and Psychosocial Needs of the Young Adult with Serious Chronic Illness, Aldershot, Avebury, 1996, 176pp. In: Journal of Advanced Nursing, 1998, 28(1), 226.

Payne S. Review of Costain Schou K & Hewison J Experiencing Cancer, Buckingham, Open University Press, 1999, 197pp. In: Health Psychology Update, 37, 23-24.

Payne S. Review of Sutherland S. A Personal Crisis and Medical Dilemma. 2nd Ed. Oxford University Press, Journal of Advanced Nursing, 1999, 30(4), 1001-1006.

Payne S. Review of Robbins M. Evaluating Palliative Care: Establishing the Evidence Base. Oxford University Press. International Journal of Palliative Nursing, 1999, 5(6), 307.

Payne S. Review of McNamara B. Fragile Lives: Death, Dying and Care. Buckingham: Open University Press. Progress in Palliative Care, 2001, 9(5), 230.

Payne S. Review of Walter T. On Bereavement: the culture of grief. Buckingham: Open University Press. Mortality, 2001, 6(2), 220-221.

Payne S. Review of Anne-Mei. The. Palliative Care and Communication: Experiences in the Clinic. Buckingham, Open University Press. In: Progress in Palliative Care 11(1), 49-50.

Payne S. Review of Mark Duman. Producing Patient Information: How to Research, Develop and Produce Effective Information Resources. London, UK: King's Fund, 2003. In: Progress in Palliative Care, 2004, 12(1), 53.

Payne S. Review of Wesley C Finegan. Trust me I'm a cancer patient. Radcliffe Medical Press. Palliative Medicine, 2004, 18(7), 671-672.

Payne S. Review of Firth, P., Luff, G. and Oliviere, D. Loss, Change and Bereavement, Cruse Bereavement Care, 2005, 24(3), 51.

Referred Published Conference Contributions

Farmer, A.J., Payne, S. and Royle, G.T. A comparative study of psychological morbidity in women with screen detected and symptomatic breast cancer. British Journal of Cancer, 65 supp XVI, 1992, 40.

Farmer, A.J., Payne, S. and Royle, G.T. A prospective study of psychological morbidity in women with screen detected and symptomatic breast cancer. The Breast, 1(3), 1992, 158.

Endall, M.J., Payne, S., Remington, R. and Royale, G.T. Detection of anxiety and depression by surgeons and significant others, in women attending a breast clinic. Psycho-Oncology, 3(2), 1994, 143.

Payne, S.A. and James, B. Lay understanding of common medical and psychological terms. Proceedings of the British Psychological Society, 2(1), 1994, 26.

Westwell, P. and Payne, S. Qualitative research: The need for adequate support. Proceedings of the British Psychological Society, 2(1), 1994, 28.

Jarrett, N. and Payne, S. Nurse-patient communication in the context of cancer care. Proceedings of the British Psychological Society, 3(1), 1995, 54.

Sque, M. and Payne, S.A. The experience of donor families. Palliative Medicine, 9(1), 1995, 68.

Fitzsimmons, D., George, S., Payne, S. and Johnson, C.D. Quality of life assessment in pancreatic cancer. European Pancreatic Club/International Association of Pancreatology, 14 June 1996, Mannheim, Germany. International Journal of Pancreatology, 19(3), 1996, 220.

Fitzsimmons, D., George, S., Payne, S. and Johnson, C.D. What worries the patient with pancreatic cancer? Palliative Care Research Forum, 6 November 1996, Coventry. Palliative Medicine, October, 1996.

Jarrett, N.J. and Payne, S. 'Comfortable' conversation: a new approach to the old topic of nurse-patient communication. Psycho-Oncology, 5(4), 1996, 355.

Payne. S. Quality demand: dilemmas for qualitative researchers. Conference proceedings for the December 1995 British Psychosocial Oncology Society Conference. Psycho‑Oncology, 5(4), 1996, 359.

Payne, S., Hillier, R. and Langley-Evans, A. The impact of witnessing death on hospice patients. Proceedings of the British Psychological Society, 4(1), 1996, 35-36.

Sque, M. and Payne, S. Dissonant loss: The experiences of donor relatives. Proceedings of the British Psychological Society, 4(1), 1996, 38.

Fitzsimmons, D., George, S., Payne, S. and Johnson, C.D. Development of a pancreatic cancer quality of life questionnaire: a grounded theory approach. Quality of Life Research, 6(7/8), 1997, 645.

Fitzsimmons, D., George, S., Payne, S. and Johnson, C.D. Multilingual development of a pancreatic cancer quality of life module to supplement the EORTC QLQ-C30. Quality of Life Research, 6(7/8), 1997, 645.

Fitzsimmons, D., George, S., Payne, S. and Johnson, C.D. Pretesting a pancreatic cancer quality of life module to supplement the QLQ-C30. Digestion, 58(2), 1997, 21(81).

Fitzsimmons, D., George, S., Payne, S. and Johnson, C.D. Quality of life in pancreatic cancer: differences in perception between health professionals and patients. Digestion, 58(2), 1997, 21(89).

Fitzsimmons, D., George, S., Payne, S. and Johnson, C.D. Quality of life in pancreatic cancer: differences in perception between health professionals and patients. Gut, 40(1), 1997, A12.

Farmer, A.J. and Payne, S.A. 'That little bit of breast cancer....' The minimization of screen detected disease: a qualitative analysis. Psycho-Oncology, 7(1), 1998, 60.

Feldman, L., Chacón, G., Payne, S. Carrasquel Y. and Blanco, G. Spillover, social support and health in working women. In: Pernille Due, M.D. ed. The Fifth International Congress of Behavioural Medicine, Abstracts, Hellerup, Denmark, International Conference Services A/S, 1998, 103.

Fitzsimmons, D., Payne, S., George, S. and Johnson, C.D. Development of a pancreatic cancer quality of life module to supplement the EORTC core cancer module the QLQ-C30. Psycho-Oncology, 7(1), 1998, 60.

Low, J.T.S., and Payne S. The good and bad death perceptions of health professionals working in palliative care. Proceedings of the British Psychological Society, 6(1), 1998, 33-34.

Low, J.T.S., Roderick, P. and Payne S. An investigation on the impact of different stroke services on carers psychological health and coping strategies. Proceedings of the British Psychological Society, 6(1), 1998, 33.

Jarrett, N. and Payne, S. 'Always look on the bright side of life...': creating and sustaining optimism in the cancer care context. Proceedings of the British Psychological Society, 6(1), 1998, 27-28.

Smith, P. and Payne S. Concerns of informal carers in palliative care. Proceedings of the British Psychological Society, 6(1), 1998, 29.

Ellis-Hill, C., Payne, S. and Ward C. An investigation of identity change and mood following stroke. Proceedings of the Society for Research in Rehabilitation Meeting, 15‑17 July 1998, University of Southampton. Clinical Rehabilitation, 13(1), 1999, 84.

Large, S., Payne, S., Jarrett, N., and Turner, P. An analysis of written information provided by hospices: a national survey. Palliative Medicine, 1999, 13: 504-505.

Payne, S., Field, D., Wiles, R., and Jarrett, N. Primary care based counsellors' experiences of bereavement counselling. Palliative Medicine, 1999 13: 505-506.

Smith, P., and Payne, S. The place of family caregivers in palliative care setting: perceptions of their role and relationship with health professionals. Palliative Medicine, 1999 13: 520-521.

Payne, S. Hospice bereavement support: the role of volunteers in New Zealand. Palliative Medicine, 1999, 13(6): 521-522.

Brown, L., Payne, S., and Royle, G. Outpatient follow-up for breast cancer patients. Psycho-oncology, 2000, 9(4): 363.

Payne, S. A critical review of the contribution of health psychology to palliative care. Proceedings of The British Psychological Society, 2000, 8(2): 43.

Dean, S., Weinman, J., Payne, S. and Smith, J. Adhering to therapeutic exercise for low back pain. Proceedings of The British Psychological Society, 2000, 8(2): 28.

Dean, S., Weinman, J., Payne, S., and Smith, J. Factors contributing to therapeutic exercise adherence for low back pain. Proceedings of The British Psychological Society, 2001, 9(1): 53.

Murphy, C., Wiles, R., Ashburn, A. and Payne, S. Communication between physiotherapists and patients in relation to recovery following stroke. Proceedings of The British Psychological Society, 2001, :71.

Ashburn, A., Wiles, R., Murphy, C., Payne, S. and Campbell, F. Communication between patients with strokes and physiotherapists. Proceedings of the Society for Research in Rehabilitation. Clinical Rehabilitation 15(4) 2001.

Payne, S. and Hardy, M. Finding a language to talk about older people: Clinical discourses used by nurses. Proceedings of the British Psychological Society 9(2), 2001: 145.

Payne, S. Balancing information needs: dilemmas in producing patient information leaflets. Health Informatics, Proceedings of the 7th International Symposium on Health Information Management Research, 2002: 16-23

May, J., Ellis-Hill, C. and Payne, S. Gate keeping and legitimisation were central in the interactions between informal carers of older people and healthcare workers. Evidence Based Nursing, 2002, 5: 95.

Payne, S., Wiles, R., Field, D. and Jarrett, N. The language and discourses of bereavement. Proceedings of the British Psychological Society 11 (1), 2003: 38.

Dean, S., Payne, S. and Weinman, J. Pain and the Professional. Proceedings of the British Psychological Society 11 (1), 2003: 121.

Hawker, S., Kerr, C. and Payne, S. End of Life Care in Community Hospitals from the Perspectives of Bereaved Family Members and Carers. Palliative Medicine, 2004 18 (2), 149-150.

Dean, S., Weinman, J. and Payne, S. Exercise Therapy for Low Back Pain: a Pragmatic Controlled Trial of a Psychological Approach to promote Adherence and Outcome. 5th Interdisciplinary World Congress on Low Back and Pelvic Pain, Melbourne, Australia, 2004 10-13, 332-335.

Skilbeck, J., Payne, S., Ingleton, C., Nolan, M., Carey, I. and Hanson, A. A Qualitative Study to Explore Family Carers. Palliative Medicine, 2004 18 (2), 151.

Payne, S., Field, D, Relf, M. and Reid, D. Hospice-Based Bereavement Services. Preliminary results of UK postal survey. Palliative Medicine, 2004 18 (2), 151-152.

Payne, S., Seymour, J., Chapman, A., Chau, R. and Lloyd, M. Attitudes and Beliefs about End-of-Life Care in the Chinese Community: Challenging Stereotypes. Palliative Medicine, 2004 18 (2), 153.

Hughes, P. M., Payne, S., Ingleton, C. and Noble, T. W. Evaluating Community Nurses' Knowledge of Palliative Care: Use of the palliative care quiz for nursing before and after an education programme. Palliative Medicine, 2004 18 (2), 156-157.

Gott, M., Payne, S., Seamark, D. and Barnes, S. Conducting a Multi-Centre Longitudinal Study within Palliative Care: Ethical and Practical Challenges. Palliative Medicine, 2004 18 (2), 168-169.

Scott, G., Steele, K., Payne, S., Ingleton, C., Nolan, M. and Carey, I. What do you mean by respite? Palliative Medicine, 2004 18 (2), 170.

Ahmed, N., Bestall, J. C., Ahmedzai, S. H., Payne, S., Clarke, D. and Noble, B. Systematic review of the problems and issues of accessing specialist palliative care by patients, carers and health and social care professionals. Palliative Medicine, 2004 18 (2), 171-172.

Payne, S., Skilbeck, J., Ingleton, C., Nolan, M. and Carey, I. Recruiting carers to palliative care studies: methodological challenges. Palliative Medicine, 2004 18 (4), 330.

Payne, S., Gott, M., Seamark, D. and Barnes, S. Practical strategies for conducting a multi-centre, longitudinal survey of palliative care needs in heart failure. Palliative Medicine, 2004 18 (4), 335.

Field D, Reid. D, Payne S and Relf M. A national postal survey of adult bereavement support in hospice and specialist palliative care services in the UK, Palliative Medicine, 2004, 18 (4), 326.

Sque M, Long T and Payne S. Organ Donation: Key Factors Influencing Families' Decision-Making, Transplantation, 2004, 78 (2), 240-241.

Payne S. Life and Death Decisions: researching the way forward. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 6-7.

Payne S, Chapman A, Seymour J and Lloyd M. "Amongst the peasants, food is placed as 'the sky'" (Chinese proverb): older Chinese people's views on food and end-of-life care. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 11.

Chapman, A., Payne, S., Seymour, J. and Lloyd, M. 'How could you have a choice?': Older Chinese people's views on cancer and palliative care choices. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 11.

Payne, S. Families - a resource for home care. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 16.

Skilbeck, J., Payne, S., Nolan, M., Ingleton, C. and Hanson, A. Respite care in the hospice setting: what do the carers think? European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 21.

Sargeant, A., Payne, S., Small, N., Gott, M. and Oliviere, D. 'Being Heard': Engaging patients and families in designing, developing and evaluating palliative care in the UK. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 48.

Payne, S., Introduction to the session on 'Families' a resource for home care? European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 49.

Reid, D., Field, D., Payne, S. and Relf, M. The use of volunteer counsellors for bereavement support in a study of bereavement services in UK hospices. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 56.

Reid, D., Field, D., Payne, S. and Relf, M. Approaches to offering adult bereavement support by Hospice Chaplains to people of diverse faiths in the UK. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 56.

Payne, S. Nursing care - what is the optimal standard? European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 72.

Payne, S. How can discourse analysis be used in palliative care? European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 75.

Froggatt, K., Payne, S. Managers' Perspectives on Death and Dying in Care Homes for Older People. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 85.

Seymour, J. ,Witherspoon, R., Gott, M., Ross, H. and Payne, S. The circumstances, experiences and preferences of older people at the end of life. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 85.

Payne, S., Hawker, S., Kerr, C., Seamark, D. and Davis, C. Palliative Care in Community Hospitals in the UK: an under recognised resource for older people. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 85.

Froggatt, K. and Payne, S. A Regulatory Perspective on the Management of Dying and Death in Care Homes for Older People. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 101.

Payne, S, Field, D., Reid, D. and Relf, M. Bereavement research: towards to common understanding of methodological and ethical issues. European Journal of Palliative Care, Abstracts of the 9th Congress of the European Association for Palliative Care (EAPC), 2005, 118.

Barnes S, Gott M, Payne S. (2005). Recruiting older people with heart failure into a study exploring palliative care needs. Poster, 9th Congress of the European Association for Palliative Care, Aachen

Sargeant, A., Payne, S., Gott, M., Small, N. and Oliviere, D. Motivational differences between service users and professionals can affect user involvement in palliative care. Palliative Medicine, 6th Palliative Care Congress, 2006, 136.

Payne, S., Chapman, A., Seymour, S. and Holloway, M. Cultural understandings of a 'good death': what criteria do older Chinese people living in the UK use? Palliative Medicine, 6th Palliative Care Congress, 2006, 138.

Barnes, S., Gott, M., Payne, S., Seamark, D., Parker, C. and Small, N. Prevalence of symptoms in a community-based sample of heart failure patients. Palliative Medicine, 6th Palliative Care Congress, 2006, 140.

Payne, S., Reid, D., Field, D. and Relf, M. Adult Hospice Bereavement Support: 'Nice' or not quite 'Nice' yet? Palliative Medicine, 6th Palliative Care Congress, 2006, 141.

Chapman, A., Payne, S., Seymour, S. and Holloway, M. Why do older Chinese people choose hospital as their preferred place to die? Palliative Medicine, 6th Palliative Care Congress, 2006, 143-144.

Reid, D., Field, D., Payne, S. and Relf, M. Adult Bereavement Support in Hospices: Sources of satisfaction amongst bereaved people. Palliative Medicine, 6th Palliative Care Congress, 2006, 145-146.

Horne, G., Seymour, J. and Payne, S. Advance Care Planning for Patients with Lung Cancer: The proposed development of a complex intervention. Palliative Medicine, 6th Palliative Care Congress, 2006, 148.

Feldman, L. and Payne, S. Palliative care services: how do they help patients and families, Bereavement support in hospices, Bereavement and loss: social and cultural dimension. 3rd National Congress of Behavioural Medicine, October 2005, VITAE 26 - Academia Biomédica Digital.htm, May 2006.

Payne S. Organisational case study methodology. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 229.

Payne S. Resilience and research: experiences of applying for project funds. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 242.

Gott, M, Barnes, S, Payne, S, Seamark, D and Small, N. Preparation for dying and views about the 'good death' in heart failure: a qualitative study with older patients and bereaved carers. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 246.

Seymour J, Payne S, Chapman A and Holloway M. End of Life Care: Experiences and attitudes of white indigenous and Chinese older people in the UK. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 250.

Chapman A, Payne S, Seymour J and Holloway M. Views about the use of traditional Chinese medicine in the UK. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 253.

Rolls L, Payne S and Relf M. Collaborative relationships: supporting the researcher in palliative care and bereavement. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 284.

Barnes S, Gott M, Payne S, Parker C and Seamark D. A study to explore characteristics, quality of life and concerns of informal carers of older people with heart failure. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 357.

Reeve J, Lloyd-Williams M, Dowrick C and Payne S. Healing narratives in people with advanced metastatic cancer. 4th Research Forum of the European Association for Palliative Care (EAPC). Palliative Medicine, 2006, 20(3), 374.

Skilbeck J, Payne S, Reid D and Davis G. Dying in old age: how illness trajectories influence place of death. 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 95.

Payne S. What is "hospice"? 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 99.

Oliviere D and Payne S. Meet the Expert Session: user Involvement and Palliative Care. 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 102.

Stevens T, Payne S, Burton C, Addington-Hall J and Jones A. Palliative care in stroke - a critical review of the literature. 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 124.

Sargeant A, Payne S, Seymour J, Ingleton C and Ward S. What are the key issues identified by Heart Failure Nurses in the UK working with patients at the end of life? 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 125.

Sargeant A, Payne S, Seymour J, Ingleton C and Ward S. How do the levels of physician contact differ between cancer and heart failure patients in Scotland during the last four weeks of life? 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 125.

Barnes S, Gott M, Payne S, Seamark D, Parker C, Small N and Gariballa S. Coping with Death and Bereavement: Views of Carers' of Older Heart Failure Patients in the UK. 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 145.

Smith P, Ramcharan P, Payne S and Chapman A. Employment and Family Caring in palliative Care Settings: A review of the literature. 10th Congress of the European Association for Palliative Care (EAPC). European Journal of Palliative Care, 2007, 156.