The participation of adult service users, including older people, in developing social care
Abel, P., Ewins, S., Hughes, M., Martin, C., Newman, P. & Teelock, G. (2002). The Good Practice Guide for Support Workers and Personal Assistants Working with Disabled People with Communication Impairments. London: Scope.
Adkins, B. & Caldwell, D. (2004). Firm or subgroup culture: where does fitting in matter most? Journal of Organizational Behavior, 25 (8): 969-978.
Afshar, H., Franks, M. & Maynard, M. (2002). Women, Ethnicity and Empowerment in Later Life.
Aldridge, J. (2007). Picture this: the use of participatory photographic research methods with people with learning disabilities. Disability & Society, 22 (1): 1-17.
Alexander, C., Edwards, R., Temple, B., with, Kanani, U., Zhuang, L., Mohib, M. & Sam, A. (2004). Access to Services with Interpreters: User Views. York: Joseph Rowntree Foundation.
Allan, K. (2001). Communication and Consultation: Exploring Ways for Staff to Involve People with Dementia in Developing Services. Bristol: The Policy Press.
Andrews, J., Manthorpe, J. & Watson, R. (2004). Involving older people in intermediate care. Journal of Advanced Nursing, 46 (3): 303-310.
Arnstein, S. (1969). A ladder of citizen participation in the USA. Journal of the American Institute of Planners, 35 (4): 214-224.
Attree, P. (2004). 'It was like my little acorn, and it's going to grow into a big tree': a qualitative study of a community support project. Health and Social Care in the Community, 12 (2): 155-161.
Attwood, M., Pedler, M., Pritchard, S. & Wilkinson, D. (2003). Leading Change: a Guide to Whole Systems Working. Bristol: Policy Press.
Audit Commission (2003). Connecting with Users and Citizens. London: Audit Commission.
Baggott, R. (2005). A funny thing happened on the way to the forum? Reforming patient and public involvement in the NHS in England. Public Administration, 83 (3): 533-551.
Baggott, R., Allsop, J. & Jones, K. (2004). Speaking for Patients and Carers: Health Consumer Groups and the Policy Process. Basingstoke: Palgrave Macmillan.
Bamber, C. & McKeown, M. (2003). Workforce development: a systematic approach to involving service users and other stakeholders. The Mental Health Review, 8 (2): 13-16.
Bamford, C. & Bruce, E. (2000). Defining the outcomes of community care: the perspectives of older people with dementia and their carers. Ageing and Society, 20 (5): 543-570.
Banongo, E., Davies, J., Godin, P., Bandit Thompson, J., Lohneis, C., Collins, D., Floyd, M., Fuller, S., Heyman, B., Reynolds, L. & Simpson, A. (2007). Engaging Service Users in the Evaluation and Development of Forensic Mental Health Services. London: City University London.
Barnes, M. (1999). Users as citizens: collective action and the local governance of welfare Social Policy and Administration, 33 (1): 73-90.
Barnes, M. (2005). The same old process? Older people, participation and deliberation. Ageing and Society, 25 (2): 245-259.
Barnes, M., Davis, A. & Rogers, H. (2006). Women's voices, women's choices: experiences and creativity in consulting women users of mental health services Journal of Mental Health, 15 (3): 329-341.
Barnes, M., Harrison, S., Mort, M. & Shardlow, P. (1999). Unequal Partners: User Groups and Community Care. Bristol: The Policy Press.
Barnes, M., Newman, J., Knops, A. & Sullivan, H. (2003). Constituting 'the public' in public participation. Public Administration, 81 (2): 379-399.
Begum, N. (2005). 'I’m Not Asking to Live Like the Queen.’ The Vision of Service Users (or Potential Service Users) and Carers who are Seldom Heard on the Future of Social Care for Adults in England. London: Social Care Institute for Excellence.
Begum, N. (2006). Doing it for Themselves: Participation and Black and Minority Ethnic Service Users. London: Social Care Institute for Excellence/REU.
Beresford, P. (1988). Consumer views: data collection or democracy? In I. Allen (Ed.), Hearing the Voice of the Consumer pp. 37-51. London: Policy Studies Institute.
Beresford, P. (2000). Service users' knowledges and social work theory: conflict or collaboration? British Journal of Social Work, 30 (4): 489-503.
Beresford, P. (2001). Service users, social policy and the future of welfare. Critical Social Policy, 21 (4): 494-512.
Beresford, P. (2002a). User involvement in research and evaluation: liberation or regulation? Social Policy and Society, 1 (2): 95-105.
Beresford, P. (2002b). User involvement: time to get serious. MCC: Building knowledge for integrated care, 10 (3): 3-4.
Beresford, P. (2005a). Redistributing profit and loss: the new economics of the market and social welfare. Critical Social Policy, 25 (4): 464-482.
Beresford, P. (2005b). 'Service user': regressive or liberatory terminology? Disability & Society, 20 (4): 469-477.
Beresford, P. & Branfield, F. (2006). Developing inclusive partnerships: user-defined outcomes, networking and knowledge − a case study. Health and Social Care in the Community, 14 (5): 436-444.
Beresford, P., Branfield, F., Taylor, J., Brennan, M., Sartori, A., Lalani, M. & Wise, G. (2006). Working together for better social work education. Social Work Education, 25 (4): 326-331.
Beresford, P. & Campbell, J. (1994). Disabled people, service users, user involvement and representation. Disability & Society, 9 (3): 315-325.
Beresford, P. & Croft, S. (2004). Service users and practitioners reunited: the key component for social work reform. British Journal of Social Work, 34 (1): 53-68.
Beresford, P. & Evans, C. (1999). Research note: research and empowerment British Journal of Social Work, 29 (5): 671-677.
Beresford, P. & Hoban, M. (2005). Participation in Anti-Poverty and Regeneration Work and Research: Overcoming Barriers and Creating Opportunities. York: Joseph Rowntree Foundation.
Beresford, P., Shamash, M., Forrest, V., Turner, M. & Branfield, F. (2005). Developing Social Care: Service Users’ Vision for Adult Support. London: Social Care Institute for Excellence.
Bickerstaff, K. & Walker, G. (2005). Shared visions, unholy alliances: power, governance and deliberative processes in local transport planning. Urban Studies, 42 (12): 2123-2144.
Bowes, A. & Sim, D. (2006). Advocacy for Black and minority ethnic communities: understandings and expectations. 36 (7): 1209-1225.
Branfield, F. & Beresford, P. (2006). Making User Involvement Work: Supporting Service User Networking and Knowledge. York: Joseph Rowntree Foundation.
Brannelly, T. (2006). Negotiating ethics in dementia care: An analysis of an ethic of care in practice. Dementia: the International Journal of Social Research and Practice, 5 (2): 197-212.
Braye, S. (2000). Participation and involvement in social care: an overview. In H. Kemshall & R. Littlechild (Eds.), User Involvement and Participation in Social Care: Research Informing Practice, pp. 9-28. London: Jessica Kingsley Publishers.
Bull, M.J., Hansen, H.E. & Gross, C.R. (2000). A professional-patient partnership model of discharge planning with elders hospitalized with heart failure. Applied Nursing Research, 13 (1): 19-28.
Butt, J. (2005). Are we there yet? Identifying the characteristics of social care organisations that successfully promote diversity. In J. Butt, B. Patel & O. Stuart (Eds.), Race Equality Discussion Papers, pp. 4-28. London: Social Care Institute for Excellence.
Butt, J. & Dhaliwal, S. (2005). Different Paths: Challenging Services. A Study of the Housing Experiences of Black and Minority Ethnic Disabled and Deaf People. London: Habinteg Housing Association/Asra Greater London Housing Association/REU.
Butt, J. & O'Neil, A. (2004). 'Let's move on': Black and minority ethnic older people's views on research findings. York: Joseph Rowntree Foundation.
Butt, J., Patel, B. & Stuart, O. (2005). Race Equality Discussion Papers. London: Social Care Institute for Excellence.
Cambridge, P. & McCarthy, M. (2001). User focus groups and Best Value in services for people with learning disabilities. Health and Social Care in the Community, 9 (6): 476-489.
Cantley, C., Steven, K. & Smith, M. (2003). 'Hear what I say’: Developing Dementia Advocacy Services. Newcastle upon Tyne: Dementia North.
Cantley, C., Woodhouse, J. & Smith, M. (2005). Listen to Us: Involving People with Dementia in Planning and Developing Services. Newcastle: Dementia North.
Carabine, J. & Monro, S. (2004). Lesbian and gay politics and participation in New Labour's Britain. Social Politics, 11 (2): 312-327.
Carpenter, J., Schneider, J., McNiven, F., Brandon, T., Stevens, R. & Wooff, D. (2004). Integration and targeting of community care for people with severe and enduring mental health problems: users' experiences of the care programme approach and care management. British Journal of Social Work, 34 (3): 313-333.
Carr, S. (2004). Has Service User Participation Made a Difference to Social Care Services? London: Social Care Institute for Excellence.
Carter, T. & Beresford, P. (2000). Age and Change. Models of Involvement for Older People. York: York Publishing Services.
Cayton, H. (2004). Telling stories: choices and challenges on the journey of dementia. Dementia: the International Journal of Social Research and Practice, 3 (1): 9-17.
Chahal, K. & Ullah, A.I. (2004). Experiencing Ethnicity: Discrimination and Service Provision. York: Joseph Rowntree Foundation. .
Charities Evaluations Services (2006). PQASSO: How to Implement a Quality Assurance System. London: Charities Evaluations Services.
Cheston, R., Bender, M. & Byatt, S. (2000). Involving people who have dementia in the evaluation of services: a review. Journal of Mental Health, 9 (5): 471-479.
Chouhan, K. & Lusane, C. (2004). Black Voluntary and Community Sector Funding, Civic Engagement and Capacity-Building. York: Joseph Rowntree Foundation.
Clare, L. & Cox, S. (2003). Improving service approaches and outcomes for people with complex needs through consultation and involvement. Disability & Society, 18 (7): 935-953.
Colley, H. & Hodkinson, P. (2001). Problems with Bridging the Gap: the reversal of structure and agency in addressing social exclusion. Critical Social Policy, 21 (3): 335-359.
Collins, A.J. (2004). Can we learn to live differently? Lessons from Going for Green: a case study of Merthyr Tydfil (South Wales). International Journal of Consumer Studies, 28 (2): 202-211.
Cornwall, A. & Gaventa, J. (2000). From users and choosers to makers and shapers: repositioning participation in social policy. Institute of Development Studies Bulletin, 31 (4): 50-62.
Craig, G., Taylor, M. & Parkes, T. (2004). Protest or partnership? The voluntary and community sectors in the policy process. Social Policy and Administration, 38 (3): 221-239.
Croft, S. & Beresford, P. (1992). The politics of participation. Critical Social Policy, 35 (1): 20-44.
Davidson, E.J. (2004). Evaluation Methodology Basics: the Nuts and Bolts of Sound Evaluation. Thousand Oaks, CA: Sage Publications, Inc.
Davies, H.T.O., Nutley, S.M. & Mannion, R. (2000). Organisational culture and quality of health care. Quality in Health Care, 9 (2): 111-119.
Davies, P. & River, L. (2005). Being Taken Seriously: The Polari in Partnership Project - Promoting Change for Older Lesbians, Gay Men and Bisexuals. London: Polari.
Department of Health (1999). National Service Framework for Mental Health. London: Department of Health.
Department of Health (2001). National Service Framework for Older People. London: Department of Health.
Department of Health (2002). Requirements for Social Work Training. London: Department of Health.
Department of Health (2005). Supporting People with Long Term Conditions: An NHS and Social Care Model to Support Local Innovation and Innovation. London: Department of Health.
Department of Health (2006a). Reward and Recognition. The Principles and Practice of Service User Payment and Reimbursement in Health and Social Care: A Guide for Service Providers, Service Users and Carers. London: Department of Health.
Department of Health (2006b). A Stronger Local Voice: A Framework for Creating a Stronger Local Voice in the Development of Health and Social Care Services. London: Department of Health.
Department of Health (2007). DH Press Release 24 January 2007: Multi-million pound social enterprise fund unveiled. London: Department of Health.
Department of Health & Farrell, C. (2004). Patient and Public Involvement in Health: The Evidence for Policy Implementation. London: Department of Health.
Department of Health/Public Services Productivity Panel (2000). Working in Partnership: Developing a Whole Systems Approach. London: HM Treasury.
Diamond, B., Parkin, G., Morris, K., Bettinis, J. & Bettesworth, C. (2003). User involvement: substance or spin? Journal of Mental Health, 12 (6): 613-626.
Disability Discrimination Act 2005. London: The Stationery Office Limited.
Duffy, J. (2006). Participating and Learning: Citizen Involvement in Social Work Education in the Northern Ireland Context. A Good Practice Guide. London: Social Care Institute for Excellence/Social Work and Social Policy (SWAP)/Northern Ireland Social Care Council (NISCC).
Duncan, P. & Thomas, S. (2000). Neighbourhood Regeneration: Resourcing Community Involvement. Bristol: Policy Press. .
Evans, C. (2004). Reflections on a model of empowered user involvement. Journal of Integrated Care, 12 (6): 22-27.
Evans, C. & Carmichael, A. (2002). Users’ Best Value: A Guide to User Involvement Good Practice in Best Value Reviews. York: York Publishing Services in association with JRF.
Evans, R. & Banton, M. (2002). Learning from Experience: Involving Black Disabled People in Shaping Services. Leamington Spa: Council of Disabled People Warwickshire.
Faulkner, A. (2004). The Ethics of Survivor Research: Guidelines for the Ethical Conduct of Research Carried out by Mental Health Service Users and Survivors: Policy Press, in association with JRF.
Fergusson, R. (2005). Discourses of exclusion: reconceptualising participation among young people. Journal of Social Policy, 33 (2): 289-320.
Fincham, R. & Rhodes, P. (2005). Organizational Behaviour (Fourth Edition), (Fourth edition). Oxford: Oxford University Press.
Fisher, M. (2002). The role of service users in problem formulation and technical aspects of social research. Social Work Education, 21 (3): 305-312.
Forbat, L. & Atkinson, D. (2005). Advocacy in practice: the troubled position of advocates in adult services. British Journal of Social Work, 35 (3): 321-335.
Francis, J. & Netten, A. (2004). Raising the quality of home care: a study of service users' views. Social Policy & Administration, 38 (3): 290-305.
Fyson, R. & Simons, K. (2003). Strategies for change: making Valuing People a reality. British Journal of Learning Disabilities, 31 (4): 153-158.
Gerrish, K. (2001). The nature and effect of communication difficulties arising from interactions between district nurses and South Asian patients and their carers. Journal of Advanced Nursing, 33 (5): 566-574.
Glasby, J. & Beresford, P. (2006). Who knows best? Evidence-based practice and the service user contribution. Critical Social Policy, 26 (1): 268-284.
Hagglund, K.J., Clark, M.J., Farmer, J.E. & Sherman, A.K. (2004). A comparison of consumer-directed and agency directed personal assistance services programmes. Disability and Rehabilitation, 26 (9): 518-527.
Harrison, S. & Mort, M. (1998). Which champions, which people? Public and user involvement in health care as a technology of legitimation. Social Policy and Administration, 32 (1): 60-70.
Health and Social Care (Community Health and Standards) Act 2003. London: The Stationery Office Limited.
Health and Social Care Act 2001. London: The Stationery Office Limited.
Heffernan, K. (2006). Social work, new public management and the language of 'service user'. British Journal of Social Work, 36 (1): 139-147.
Her Majesty's Government/Department of Health (2006). Our Health, Our Care, Our Say: a New Direction for Community Services, Cm 6737. London: Department of Health.
Hodge, S. (2005). Participation, discourse and power: a case study in service user involvement. Critical Social Policy, 25 (2): 164-179.
Hofstede, G. (1998). Identifying organizational subcultures: an empirical approach. Journal of Management Studies, 35 (1): 1-12.
Hughes, D. (1996). NHS managers as rhetoricians: a case of culture management? Sociology of Health and Illness, 18 (3): 291-314.
Hyde, P. & Davies, H.T.O. (2004). Service design, culture and performance: collusion and co-production in health care. Human Relations, 57 (11): 1407-1426.
Joyce, T. & Shuttleworth, L. (2001). From engagement to participation: How do we bridge the gap? British Journal of Learning Disabilities, 29 (2): 63-71.
Kirby, P., Lanyon, C., Cronin, K. & Sinclair, R. (2003a). Building a Culture of Participation: Involving Children and Young People in Policy, Service Planning, Delivery and Evaluation: Handbook. London: Department for Education and Skills.
Kirby, P., Lanyon, C., Cronin, K. & Sinclair, R. (2003b). Building a Culture of Participation: Involving Children and Young People in Policy, Service Planning, Delivery and Evaluation: Research Report. London: Department for Education and Skills.
Kotecha, N., Fowler, C., Donskoy, A.-L., Johnson, P., Shaw, T. & Doherty, K. (2007). A Guide to User-Focused Monitoring: Setting up and Running a Project. London: Sainsbury Centre for Mental Health.
Lewington, W. & Clipson, C. (2003). Advocating for Equality. London: Scope.
Lister, R. (1998). Citizen in action: citizenship and community development in a Northern Ireland context. Community Development Journal, 33 (3): 226-235.
Lunch, N. & Lunch, C. (2006). Insights into Participatory Video: a Handbook for the Field. Oxford: Insight.
Macaulay, A.C., Commanda, L.E., Freeman, W.L., Gibson, N., McCabe, M.L., Robbins, C.M. & Twohig, P.L. (1999). Participatory research maximises community and lay involvement. British Medical Journal, 319 (7212): 774-778.
Manthorpe, J., Clough, R., Cornes, M., Bright, L., Moriarty, J., Iliffe, S. & OPRSI (Submitted). Four years on: the impact of the National Service Framework for Older People on the experiences, expectations and views of older people.
Miller, E., Cook, A., Alexander, H., Cooper, S.A., Hubbard, G., Morrison, J. & Petch, A. (2006). Challenges and strategies in collaborative working with service user researchers: reflections from the academic researcher. Research Policy and Planning, 24 (3): 197-208.
Millward, L. (2005). 'Just because we are amateurs doesn't mean we aren't professional': the importance of expert activists in tenant participation. Public Administration, 83 (3): 735-751.
Mitchell, R. (2005). 'I'm tickled that I took that photo'. Journal of Dementia Care, 13 (2): 14.
Modood, T., Berthoud, R., Lakey, J., Smith, P., Virdee, S. & Beishon, S. (1997). Ethnic Minorities in Britain. Diversity and Disadvantage. London: Policy Studies Institute.
Mordey, M. & Crutchfield, J. (2004). User involvement in supported housing. Housing, Care and Support, 7 (1): 7-10.
Moriarty, J., Manthorpe, J., Price, L., Cornes, M., Clough, R., Bright, L., Iliffe, S. & Older People Researching Social Issues (2006). 'Rights and regulation: adding diversity in inspections of older people’s services (conference paper)'. Paper presented at Sexuality in social work and social care: critical thinking and new approaches, South Bank University, London.
Morris, J. (2005). Citizenship and disabled people: a scoping paper prepared for the Disability Rights Commission. London: Disability Rights Commission.
National AIDS Trust (2006). Public Attitudes Towards HIV. London: National AIDS Trust..
National Audit Office (2004). Getting Citizens Involved: Community Participation in Neighbourhood Renewal. London: The Stationery Office.
National Health Service Reform and Health Care Professions Act 2002. London: The Stationery Office Limited.
Newman, J. (2002). Modernising Government: New Labour, Policy and Society. London: Sage Publications Ltd.
Newman, J., Barnes, M., Sullivan, H. & Knops, A. (2004). Public participation and collaborative governance. Journal of Social Policy, 33 (2): 203-223.
O'Keefe, E. & Hogg, C. (1999). Public participation and marginalized groups: the community development model. Health Expectations, 2 (4): 245-254.
Parasuraman, A., Berry, L.L. & Zeithaml, V.A. (1988). SERVQUAL: A multiple-item scale for measuring consumer perceptions of service quality. Journal of Retailing, 64 (1): 12-40.
Parasuraman, A., Berry, L.L. & Zeithaml, V.A. (1991). Refinement and reassessment of the SERVQUAL scale. Journal of Retailing, 67 (4): 420-450.
Patmore, C. (2001). Can managers research their own services? An experiment in consulting frail, older community care clients Managing Community Care, 9 (5): 8-17.
Patton, M.Q. (2001). Qualitative Research & Evaluation Methods, (3rd edition). Thousand Oaks, CA: Sage Publications, Inc.
Pawson, R., Boaz, A., Grayson, L., Long, A. & Barnes, C. (2003). Types and Quality of Knowledge in Social Care. London: Social Care Institute for Excellence.
Pinfold, V., Byrne, P. & Toulmin, H. (2005). Challenging stigma and discrimination in communities: a focus group study identifying UK mental health service users' main campaign priorities. International Journal of Social Psychiatry, 51 (2): 128-138.
Porter, J., Parsons, S. & Robertson, C. (2006). Time for review: supporting the work of an advisory group. Journal of Research in Special Educational Needs, 6 (1): 11-16.
Postle, K. & Beresford, P. (2007). Capacity building and the reconception of political participation: a role for social care workers? . British Journal of Social Work, 37 (1): 143-158.
Postle, K., Wright, P. & Beresford, P. (2005). Older people's participation in political activity - making their voices heard: a potential support role for welfare professionals in countering ageism and social exclusion. Practice, 17 (3): 173-189.
Proctor, G. (2001). Listening to older women with dementia: relationships, voices and power. Disability and Society, 16 (3): 361-376.
Rapaport, J., Manthorpe, J., Moriarty, J., Hussein, S. & Collins, J. (2005). Advocacy and people with learning disabilities in the UK: how can local funders find value for money? Journal of Intellectual Disabilities, 9 (4): 299-319.
Raynes, N.V. (1998). Involving residents in quality specification. Ageing and Society, 18 (1): 65-78.
Reed, J., Stanley, D. & Clarke, C. (2004a). Health, Well-being and Older People. Bristol: Policy Press.
Reed, J., Weiner, R. & Cook, G. (2004b). Partnership research with older people - moving towards making the rhetoric a reality. Journal of Clinical Nursing, 13 (s1): 3-10.
Roberts, K. (2002). Exploring participation: older people on discharge from hospital. Journal of Advanced Nursing, 40 (4): 413-420.
Robson, P., Begum, N. & Locke, M. (2003). Developing User Involvement: Working Towards User-Centred Practice in Voluntary Organisations Bristol: The Policy Press.
Rose, D. (2003). Collaborative research between users and professionals: peaks and pitfalls. Psychiatric Bulletin, 27 (11): 404-406.
Roulstone, A., Hudson, V., Kearney, J., Martin, A., with & Warren, J. (2006). Working Together: Carer Participation in England, Wales and Northern Ireland. London: Social Care Institute for Excellence.
Rummery, K. & Glendinning, C. (2000). Access to services as a civil and social rights issue: the role of welfare professionals in regulating access to and commissioning services for disabled and older people under New Labour. Social Policy and Administration, 34 (5): 529-550.
Rutter, D., Manley, C., Weaver, T., Crawford, M.J. & Fulop, N. (2004). Patients or partners? Case studies of user involvement in the planning and delivery of adult mental health services in London. Social Science & Medicine, 58 (10): 1973-1984.
Scriven, M. (1991). Evaluation Thesaurus, (3rd edition). Thousand Oaks, CA: Sage Publications, Inc.
Secretary of State for Health (2001). Valuing People: A New Strategy for Learning Disability for the 21st Century, CM 5086. London: The Stationery Office.
Simmons, R. & Birchall, J. (2005). A joined-up approach to user participation in public services: strengthening the "participation chain". Social Policy and Administration, 39 (3): 260-283.
Smith, R. (2004). A matter of trust: service users and researchers. Qualitative Social Work, 3 (3): 335-346.
Stalker, K. (1998). Some ethical and methodological issues in research with people with learning difficulties Disability & Society, 13 (1): 5-19.
Stickley, T. (2006). Should service user involvement be consigned to history? A critical realist perspective. Journal of Psychiatric and Mental Health Nursing, 13 (5): 570-577.
Taylor, D. (2005). Governing through evidence: participation and power in policy evaluation. Journal of Social Policy, 34 (4): 601-618.
Taylor, M., Purdue, D., Carlton, N., Mackridge, R., Syed, A., Ardron, R., Wilson, M., Meegan, R. & Russell, H. (2005). Making Connections: An Evaluation of the Community Participation Programmes. London: Neighbourhood Renewal Unit..
Tew, J. (2006). Understanding power and powerlessness: towards a framework for emancipatory practice in social work. Journal of Social Work, 6 (1): 33-51.
Townsley, R., Howarth, J., Graham, M. & LeGrys, P. (2002). Committed to Change? Promoting the Involvement of People with Learning Difficulties in Staff Recruitment. Bristol: Policy Press in association with JRF.
Truman, C. & Raine, P. (2002). Experience and meaning of user involvement: some explorations from a community mental health project. Health & Social Care in the Community, 10 (3): 136-143.
Turner, M. & Beresford, P. (2005). Contributing on Equal Terms: Service User Involvement and the Benefits System. London: Social Care Institute for Excellence.
Turner, M., Brough, P. & Williams-Findlay, R.B. (2003). Our Voice in our Future: Service Users Debate the Future of the Welfare State. York: Joseph Rowntree Foundation.
Twigg, J. (2000). The changing role of users and carers. In B. Hudson (Ed.), The Changing Role of Social Care, pp. 103-119. London: Jessica Kingsley Publishers.
Waldman, J. (2005). Using evaluative research to support practitioners and service users in undertaking reflective writing for public dissemination. British Journal of Social Work, 35 (6): 975-981.
Wallcraft, J., with, Read, J. & Sweeney, A. (2003). On Our Own Terms: Users and Survivors of Mental Health Services Working Together for Support and Change. London: Sainsbury Centre for Mental Health.
Wallerstein, N. What is the evidence on effectiveness of empowerment to improve health? Copenhagen: WHO Regional Office for Europe.
Walmsley, J. (2004). Involving users with learning difficulties in health improvement: lessons from inclusive learning disability research. Nursing Inquiry, 11 (1): 54-64.
Wang, C.C. (1999). Photovoice: a participatory action research strategy applied to women's health. Journal of Womens Health, 8 (2): 185-192.
Waterson, J. & Morris, K. (2005). Training in 'social ' work: exploring issues of involving users in teaching on social work degree programmes. Social Work Education, 24 (6): 653-675.
Weeks, L., Shane, C., MacDonald, F., Hart, C. & Smith, R. (2006). Learning from the experts: people with learning difficulties training and learning from each other. British Journal of Learning Disabilities, 34 (1): 49-55.
Wilkinson, H. (Ed.) (2002). The Perspectives of People with Dementia: Research Methods and Motivations. London: Jessica Kingsley Publishers.
Wilson, A. & Beresford, P. (2000). 'Anti-oppressive practice': emancipation or appropriation? British Journal of Social Work, 30 (5): 553-573.
Wisniewski, M. (2001). Using SERVQUAL to assess customer satisfaction with public sector services. Managing Service Quality, 11 (6): 380-388.
Wistow, G. (2005). Developing Social Care: the Past, the Present and the Future. London: Social Care Institute for Excellence.
Wright, P., Turner, C., Clay, D. & Mills, H. (2006). The Participation of Children and Young People in Developing Social Care. London: Social Care Institute for Excellence.