Consumer‐driven health care
Building partnerships in research
Bibliographic Data
| ID | 19508976 |
|---|---|
| Authors | Beverley Shea (0000-0002-7686-2585, University of Ottawa, corresponding author), Nancy Santesso (0000-0003-0550-4585, University of Ottawa), Ann Qualman (Cochrane), Turid Heiberg (Diakonhjemmet Hospital), Amye Leong (0000-0002-9948-7407), Maria Judd (University of Ottawa), Vivian Robinson (University of Ottawa), George A Wells (0000-0002-2289-9139, University of Ottawa), George Wells (0000-0002-9100-1628), Peter Tugwell (0000-0001-5062-0556, University of Ottawa) |
| Year | 2005 |
| Volume | 8 |
| Issue | 4 |
| Pages | 352-359 |
| Publication date | 2005-12-01 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Health Expectations (JOURNAL) |
| Journal identifiers | ISSN: 1369-6513 • E-ISSN: 1369-7625 |
| Publisher | Wiley (PUBLISHER • GB) |
| DOI | 10.1111/j.1369-7625.2005.00347.x |
| PMID | 16266423 |
| OpenAlex | W1995433954 |
| Language | EN |
| Citations received | 18 |
| References cited | 2 |
Over the past four decades, there has been a widespread movement to increase the involvement of patients and the public in health care. Strategies to effectively foster consumer participation are occurring within all research activities from research priority setting to utilization. One of the ten principles of the Cochrane Collaboration is to ‘enable wide participation’, and this includes consumers. The Cochrane Musculoskeletal Group (CMSG) is a review group of 50 within the Collaboration that has been working to increase consumer participation since its inception in 1993. Based in Canada, the CMSG has embraced the concept of knowledge translation as advocated by the Canadian Institutes of Health Research. The emphasis in knowledge translation is on interactions or partnerships between researchers and users to facilitate the use of relevant research in decision making. While the CMSG recognizes the importance of reaching all users, much of its work has focused on developing relationships with people with musculoskeletal diseases to enhance consumer participation in research. The CMSG has built a network of consumer members who guide research priorities, peer review systematic reviews and also promote and facilitate consumer‐appropriate knowledge dissemination. Consumers were recruited through links with other arthritis organizations and the recruitment continues. Specific roles were established for the consumer team and responsibilities of the CMSG staff developed. The continuing development of a diversified team of consumer participants enables the CMSG to produce and promote access to high quality relevant systematic reviews and summaries of those reviews to the consumer
Business · Health care · Knowledge management · Knowledge translation · Medical education · Political science · Public relations · Clinical practice guidelines implementation · Engineering · Health Policy Implementation Science · Medicine · Mental Health and Patient Involvement · Psychology · Marketing
Translating Knowledge Directly to Childbearing Women
A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities
System-Wide and Group-Specific Health Service Improvements
What becomes of social science knowledge
The staged addiction
Consumer involvement in systematic reviews of comparative effectiveness research
Patient-expert partnerships in research
Clarifying the mechanisms and resources that enable the reciprocal involvement of seldom heard groups in health and social care research
Involvement of the consumer voice
Mapping the impact of patient and public involvement on health and social care research
Improving the quality of prison research
PartecipaSalute, an Italian project to involve lay people, patients’ associations and scientific‐medical representatives in the health debate
Do not forget the professional – the value of the FIRST model for guiding the structural involvement of patients in rheumatology research
Do different stakeholder groups share mental health research priorities? A four‐arm Delphi study
The Cochrane Library review titles that are important to users of health care, a Cochrane Consumer Network project
Collaboration and co‐ownership in research
Patient and service user engagement in research
Patient involvement in health research
| Citations per year | 0.9 |
|---|---|
| Citation span | 2006 - 2025 (20) |
| Highly cited | No |