Engaging older adults in healthcare research and planning: a realist synthesis
暂无分享,去创建一个
Paul Stolee | Heather McNeil | Jacobi Elliott | Jennifer D. Walker | P. Stolee | H. McNeil | J. Elliott | G. Heckman | Jennifer Walker | George Heckman | Jessica Ashbourne | Kelsey Huson | Kelsey Huson | J. Ashbourne
[1] Eva Lidén,et al. Patient participation in discharge planning conference , 2014, International journal of integrated care.
[2] S. Oliver,et al. Consumer involvement in the health technology assessment program , 2004, International Journal of Technology Assessment in Health Care.
[3] Rebecca R. Cheezum,et al. Community-based participatory research: a capacity-building approach for policy advocacy aimed at eliminating health disparities. , 2010, American journal of public health.
[4] E. Yuen,et al. Partnering to Collect Health Services and Public Health Data in Hard-to-Reach Communities: A Community-Based Participatory Research Approach for Collecting Community Health Data , 2010, Progress in community health partnerships : research, education, and action.
[5] C. Gwede,et al. Designing a Community-Based Lay Health Advisor Training Curriculum to Address Cancer Health Disparities , 2013, Health promotion practice.
[6] Paul Dieppe,et al. Relation between agendas of the research community and the research consumer , 2000, The Lancet.
[7] H. Dawkins,et al. Informing public health policy through deliberative public engagement: perceived impact on participants and citizen-government relations. , 2013, Genetic testing and molecular biomarkers.
[8] G. Gargioni. Community healthcare programmes: empowering people to improve access to prevention and care , 2010 .
[9] P. Tobin,et al. Community-based health research led by the Vuntut Gwitchin First Nation , 2011, International journal of circumpolar health.
[10] M. Ford,et al. Training Partnership Dyads for Community-Based Participatory Research , 2013, Health promotion practice.
[11] S. Couzos,et al. ‘We are Not Just Participants—We are in Charge’: The NACCHO Ear Trial and the Process for Aboriginal Community-controlled Health Research , 2005, Ethnicity & health.
[12] William M. K. Trochim,et al. Concept mapping: an introduction to structured conceptualization in health care. , 2005, International journal for quality in health care : journal of the International Society for Quality in Health Care.
[13] C. Jenkins,et al. Beyond the Medical Model: Interdisciplinary Programs of Community‐Engaged Health Research , 2011, Clinical and translational science.
[14] Ray Pawson,et al. RAMESES publication standards: realist syntheses , 2013, BMC Medicine.
[15] D. Gough,et al. Clarifying differences between review designs and methods , 2012, Systematic Reviews.
[16] Paul Meissner,et al. A New Taxonomy for Stakeholder Engagement in Patient-Centered Outcomes Research , 2012, Journal of General Internal Medicine.
[17] S. Arnstein,et al. Ladder of Citizen Participation , 2020 .
[18] A. Draper,et al. Using Participatory Approaches with Older People in a Residential Home in Guyana: Challenges and Tensions , 2012, Journal of Cross-Cultural Gerontology.
[19] S. Glouberman,et al. Choosing Healthcare Options by Involving Canada's Elderly: a protocol for the CHOICE realist synthesis project on engaging older persons in healthcare decision-making , 2015, BMJ Open.
[20] C. Grogan,et al. Residents' perceptions of effective community representation in local health decision-making. , 2012, Social science & medicine.
[21] M. Holosko,et al. How service users become empowered in human service organizations: the empowerment model. , 2001, International journal of health care quality assurance incorporating Leadership in health services.
[22] A. Tricco,et al. What is the most appropriate knowledge synthesis method to conduct a review? Protocol for a scoping review , 2012, BMC Medical Research Methodology.
[23] C-L Huang,et al. Community health development: what is it? , 2005, International nursing review.
[24] Jonathan Sussman,et al. Of time and troubles: Patient involvement and the production of health care disparities , 2012, Health.
[25] Norma Daykin,et al. Developing user involvement in a UK cancer network: professionals’ and users’ perspectives , 2004 .
[26] Nicole Ruggiano. Consumer Direction in Long-Term Care Policy: Overcoming Barriers to Promoting Older Adults' Opportunity for Self-Direction , 2012, Journal of gerontological social work.
[27] Colin Camerer,et al. Not So Different After All: A Cross-Discipline View Of Trust , 1998 .
[28] N. Goodwin,et al. What are the principles that underpin integrated care? , 2014, International journal of integrated care.
[29] M. Fitch,et al. From Patient to Participant: Enhancing the Validity and Ethics of Cancer Research through Participatory Research , 2013, Journal of Cancer Education.
[30] G. White,et al. Consumers as Collaborators in Research and Action , 2001, People with Disabilities.
[31] Broden Giambrone,et al. 'About time!' Insights from Research with Pride: a community-student collaboration. , 2012, Health promotion international.
[32] V. Dickson-Swift,et al. Community participation in rural health: a scoping review , 2013, BMC Health Services Research.
[33] Douglas D. Perkins. Speaking truth to power: Empowerment ideology as social intervention and policy , 1995, American journal of community psychology.
[34] L. London,et al. Implementing community participation through legislative reform: a study of the policy framework for community participation in the Western Cape province of South Africa , 2012, BMC International Health and Human Rights.
[35] J. Higgins. Closer to Home: The Case for Experiential Participation in Health Reform , 1999, Canadian Journal of Public Health.
[36] G. Heckman. Integrated care for the frail elderly. , 2011, HealthcarePapers.
[37] Trudy van der Weijden,et al. Patient and public involvement in clinical guidelines: international experiences and future perspectives , 2010, Quality and Safety in Health Care.
[38] A. Nauta,et al. Factors predicting trust between GPs and OPs , 2001, International journal of integrated care.
[39] K. Middleton,et al. Patients’ and Community Leaders’ Perceptions Regarding Conducting Health Behavior Research in a Diverse, Urban Clinic Specializing in Rheumatic Diseases , 2012, Progress in community health partnerships : research, education, and action.
[40] A. Casebeer,et al. Will it make a difference if I show up and share? A citizens' perspective on improving public involvement processes for health system decision-making , 2004, Journal of health services research & policy.
[41] J. Slaets,et al. Inclusion of frail elderly patients in clinical trials: solutions to the problems. , 2013, Journal of geriatric oncology.
[42] H. V. van Stel,et al. Multidisciplinary integrated Parent and Child Centres in Amsterdam: a qualitative study , 2013, International journal of integrated care.
[43] Engaging the Deaf American Sign Language Community: Lessons From a Community-Based Participatory Research Center , 2012, Progress in community health partnerships : research, education, and action.
[44] D. Wilkin,et al. Are primary care groups and trusts consulting local communities? , 2002, Health & social care in the community.
[45] P. Powell,et al. From tokenism to meaningful engagement: best practices in patient involvement in an EU project , 2015, Research Involvement and Engagement.
[46] D. Lüdecke. Patient centredness in integrated care: results of a qualitative study based on a systems theoretical framework , 2014, International journal of integrated care.
[47] J Gabbay,et al. Involving consumers in research and development agenda setting for the NHS: developing an evidence-based approach. , 2004, Health technology assessment.
[48] T. Greenhalgh,et al. Realist review - a new method of systematic review designed for complex policy interventions , 2005, Journal of health services research & policy.
[49] H. Kendig,et al. Involving older people in community‐based research: Developing a guiding framework for researchers and community organisations , 2009, Australasian journal on ageing.
[50] J. Boote,et al. What does it mean to involve consumers successfully in NHS research? A consensus study , 2004, Health expectations : an international journal of public participation in health care and health policy.
[51] Moving beyond good intentions: Indigenous participation in Aboriginal and Torres Strait Islander health research , 2005, Australian and New Zealand journal of public health.
[52] I. Graham. Knowledge synthesis and the Canadian Institutes of Health Research , 2012, Systematic Reviews.
[53] Sally Brearley,et al. Involving older people in research: methodological issues. , 2005, Health & social care in the community.
[54] W. Doherty,et al. Citizen health care: A model for engaging patients, families, and communities as coproducers of health. , 2006 .
[55] B. Israel,et al. Can communities and academia work together on public health research? Evaluation results from a community-based participatory research partnershipin detroit , 2001, Journal of Urban Health.
[56] Roland Bal,et al. Inter-organisational communication networks in healthcare: centralised versus decentralised approaches , 2007, International journal of integrated care.
[57] Andrew D Oxman,et al. SUPPORT Tools for evidence-informed health Policymaking (STP) 15: Engaging the public in evidence-informed policymaking , 2009, Health research policy and systems.
[58] M. Markle-Reid,et al. Interprofessional partnerships in chronic illness care: a conceptual model for measuring partnership effectiveness , 2008, International journal of integrated care.
[59] Douglas G. Altman,et al. Practical statistics for medical research , 1990 .
[60] J. Grimshaw,et al. Understanding the relationship between the perceived characteristics of clinical practice guidelines and their uptake: protocol for a realist review , 2011, Implementation science : IS.
[61] J. Sloan,et al. Patient engagement in research: a systematic review , 2014, BMC Health Services Research.
[62] T. Abma,et al. Patient issues in health research and quality of care: an inventory and data synthesis , 2013, Health expectations : an international journal of public participation in health care and health policy.
[63] M. Slade,et al. The contribution of advisory committees and public involvement to large studies: case study , 2010, BMC health services research.
[64] Carol R. Horowitz,et al. Community-Based Participatory Research From the Margin to the Mainstream: Are Researchers Prepared? , 2009, Circulation.
[65] Sandy Oliver,et al. Patients’ and clinicians’ research priorities , 2011, Health expectations : an international journal of public participation in health care and health policy.
[66] Charlotte Paterson,et al. 'Take small steps to go a long way' consumer involvement in research into complementary and alternative therapies. , 2004, Complementary therapies in nursing & midwifery.
[67] C. Charles,et al. From rhetoric to reality: including patient voices in supportive cancer care planning , 2005, Health expectations : an international journal of public participation in health care and health policy.
[68] Trisha Greenhalgh,et al. Protocol - realist and meta-narrative evidence synthesis: Evolving Standards (RAMESES) , 2011, BMC medical research methodology.
[69] J. Boote,et al. Public involvement in the systematic review process in health and social care: a narrative review of case examples. , 2011, Health policy.
[70] S. Staniszewska,et al. The PRIME project: developing a patient evidence‐base , 2010, Health expectations : an international journal of public participation in health care and health policy.
[71] K. Graham,et al. Community Action Research: Who Does What to Whom and Why? Lessons Learned from Local Prevention Efforts (International Experiences) , 2000, Substance use & misuse.
[72] M. D. de Wit,et al. European League Against Rheumatism recommendations for the inclusion of patient representatives in scientific projects , 2011, Annals of the Rheumatic Diseases.
[73] J. Sweeney,et al. Patient and family engagement: a framework for understanding the elements and developing interventions and policies. , 2013, Health affairs.
[74] N. Lightfoot,et al. Thinking outside the box: Aboriginal people's suggestions for conducting health studies with Aboriginal communities. , 2011, Public health.
[75] Peter J. Smith. A transdisciplinary approach to research on work and health: What is it, what could it contribute, and what are the challenges? , 2007 .
[76] T. Greenhalgh,et al. Realist synthesis - an introduction , 2004 .
[77] S. Jaglal,et al. Communicating during care transitions for older hip fracture patients: family caregiver and health care provider's perspectives , 2013, International journal of integrated care.
[78] A. Adams,et al. Learning to work together: developing academic and community research partnerships. , 2004, WMJ : official publication of the State Medical Society of Wisconsin.
[79] J. Morone,et al. Power to the People? Restoring Citizen Participation , 2003, Journal of health politics, policy and law.
[80] K. Dickersin,et al. Consumer involvement in systematic reviews of comparative effectiveness research , 2013, Health expectations : an international journal of public participation in health care and health policy.
[81] S. Harrison,et al. Involving patients in research: setting up a service users' advisory group. , 2001, Journal of management in medicine.
[82] J. Andrews,et al. Partnership readiness for community-based participatory research. , 2012, Health education research.
[83] A. Mühlbacher,et al. Patient-centredness in integrated healthcare delivery systems - needs, expectations and priorities for organised healthcare systems , 2013, International journal of integrated care.
[84] J. Lenaghan,et al. Involving the public in rationing decisions. The experience of citizens juries. , 1999, Health policy.