about
The Keele community knee pain forum: action research to engage with stakeholders about the prevention of knee pain and disabilityExploring perceived barriers, drivers, impacts and the need for evaluation of public involvement in health and social care research: a modified Delphi study.Mapping the impact of patient and public involvement on health and social care research: a systematic reviewConsumer input into research: the Australian Cancer Trials website.A systematic review of the impact of patient and public involvement on service users, researchers and communities.Operationalising a model framework for consumer and community participation in health and medical researchEthical issues in mental health research: the case for community engagementEngaging people who use drugs in policy and program development: a review of the literature.Impact on the individual: what do patients and carers gain, lose and expect from being involved in research?Involving lay and professional stakeholders in the development of a research intervention for the DEPICTED study.Patient involvement in research priorities (PIRE): a study protocolEthical, strategic and meaningful involvement of women living with HIV starts at the beginning.User involvement in the development of a research bid: barriers, enablers and impacts.Can the impact of public involvement on research be evaluated? A mixed methods study.Can research development bursaries for patient and public involvement have a positive impact on grant applications? A UK-based, small-scale service evaluation.Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study.Series: The research agenda for general practice/family medicine and primary health care in Europe. Part 5: Needs and implications for future research and policy.Evaluating patient and stakeholder engagement in research: moving from theory to practice.Building capacity for service user and carer involvement in research: the implications and impact of best research for best health.Youth Speak: increasing engagement of young people in mental health research.Improving the quality of prison research: A qualitative study of ex-offender service user involvement in prison suicide prevention research.'I'm sure we made it a better study…': Experiences of adults with intellectual disabilities and parent carers of patient and public involvement in a health research study.Assessing the organizational impact of patient involvement: a first STEPP.A stronger voice.It's not just 'What' you do, it's also the 'Way' that you do it: Patient and Public Involvement in the Development of Health Research.Lone voices have an emotional content: focussing on mental health service user and carer involvement.Consumers and carers as partners in mental health research: reflections on the experience of two project teams in Victoria, Australia.Identifying the patient perspective of the quality of mental healthcare for common chronic problems: a qualitative study.Service user reflections on the impact of involvement in research.Perceived Significance of Engagement in Research Prioritization Among Chronic Kidney Disease Patients, Caregivers, and Health Care Professionals: A Qualitative Study
P2860
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P2860
description
2005 nî lūn-bûn
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2005年の論文
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2005年論文
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2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
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2005年论文
@zh-cn
name
The impact of service user involvement in research.
@ast
The impact of service user involvement in research.
@en
type
label
The impact of service user involvement in research.
@ast
The impact of service user involvement in research.
@en
prefLabel
The impact of service user involvement in research.
@ast
The impact of service user involvement in research.
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P2093
P2860
P1476
The impact of service user involvement in research.
@en
P2093
Jean Boness
John Girdlestone
Virginia Minogue
P2860
P304
P356
10.1108/09526860510588133
P577
2005-01-01T00:00:00Z