Literature DB >> 15526385

Will it make a difference if I show up and share? A citizens' perspective on improving public involvement processes for health system decision-making.

Julia Abelson1, Pierre-Gerlier Forest, Ann Casebeer, Gail Mackean.   

Abstract

INTRODUCTION: Health policy decision-makers are grappling with increasingly complex and ethically controversial decisions at a time when citizens are demanding more involvement in these decision processes.
OBJECTIVES: To assess and revise a set of guiding principles for the design of public involvement processes generated from a synthesis of public participation design and evaluation frameworks that can be used to inform the design and evaluation of future public participation processes in the health sector.
METHODS: Six focus groups held in five Canadian provinces comprising citizens with considerable experience of public participation processes. RESULTS AND DISCUSSION: Our findings suggest that citizen participants are highly critical of, and discerning about,their public participation experiences. Yet, they are optimistic and determined to contribute in meaningful ways to future public policy processes. They are clear about where improvements are needed and give top priority to what information is shared, and how, among participants and decision-makers. The views of experienced citizens mapped well onto most of the prior principles of public involvement with a few modifications. First, participants gave greater emphasis to the content and balance of information for the purposes of building trust and credibility between citizens and decision-makers. Second, participants viewed themselves, as well as decision-makers, as sources of information to be shared through the consultation process. Finally, participants stressed the importance of getting the information and communication principles right over addressing all other principles.

Entities:  

Mesh:

Year:  2004        PMID: 15526385     DOI: 10.1258/1355819042250203

Source DB:  PubMed          Journal:  J Health Serv Res Policy        ISSN: 1355-8196


  14 in total

1.  The integration of citizens into a science/policy network in genetics: governance arrangements and asymmetry in expertise.

Authors:  Geneviève Daudelin; Pascale Lehoux; Julia Abelson; Jean L Denis
Journal:  Health Expect       Date:  2010-10-28       Impact factor: 3.377

2.  From rhetoric to reality: including patient voices in supportive cancer care planning.

Authors:  Sara K Tedford Gold; Julia Abelson; Cathy A Charles
Journal:  Health Expect       Date:  2005-09       Impact factor: 3.377

3.  Involving patients in health technology funding decisions: stakeholder perspectives on processes used in Australia.

Authors:  Edilene Lopes; Jackie Street; Drew Carter; Tracy Merlin
Journal:  Health Expect       Date:  2015-02-21       Impact factor: 3.377

4.  Inclusivity and dementia: health services planning with individuals with dementia: effective inclusion requires action at multiple levels by individuals with dementia, care partners, service providers and funding organizations.

Authors:  Kyle Whitfield; Susan Wismer
Journal:  Healthc Policy       Date:  2006-01

5.  Consumers' perspectives on national health insurance in South Africa: using a mobile health approach.

Authors:  Edda Weimann; Maria C Stuttaford
Journal:  JMIR Mhealth Uhealth       Date:  2014-10-28       Impact factor: 4.773

Review 6.  Engaging older adults in healthcare research and planning: a realist synthesis.

Authors:  Heather McNeil; Jacobi Elliott; Kelsey Huson; Jessica Ashbourne; George Heckman; Jennifer Walker; Paul Stolee
Journal:  Res Involv Engagem       Date:  2016-03-07

Review 7.  Giving voice to older adults living with frailty and their family caregivers: engagement of older adults living with frailty in research, health care decision making, and in health policy.

Authors:  Jayna Holroyd-Leduc; Joyce Resin; Lisa Ashley; Doris Barwich; Jacobi Elliott; Paul Huras; France Légaré; Megan Mahoney; Alies Maybee; Heather McNeil; Daryl Pullman; Richard Sawatzky; Paul Stolee; John Muscedere
Journal:  Res Involv Engagem       Date:  2016-06-17

8.  A knowledge synthesis of patient and public involvement in clinical practice guidelines: study protocol.

Authors:  France Légaré; Antoine Boivin; Trudy van der Weijden; Christine Packenham; Sylvie Tapp; Jako Burgers
Journal:  Implement Sci       Date:  2009-06-04       Impact factor: 7.327

9.  Knowledge translation research in population health: establishing a collaborative research agenda.

Authors:  Christian Dagenais; Valéry Ridde; Marie-Claire Laurendeau; Karine Souffez
Journal:  Health Res Policy Syst       Date:  2009-12-10

10.  Taking stock of current societal, political and academic stakeholders in the Canadian healthcare knowledge translation agenda.

Authors:  Mandi S Newton; Shannon Scott-Findlay
Journal:  Implement Sci       Date:  2007-10-04       Impact factor: 7.327

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