How to engage patients in research and quality improvement in community-based primary care settings: Protocol for a participatory action research pilot study

被引:9
|
作者
Haesebaert J. [1 ,2 ]
Samson I. [3 ]
Lee-Gosselin H. [4 ]
Guay-Bélanger S. [1 ]
Proteau J.-F. [5 ]
Drouin G. [5 ]
Guimont C. [5 ]
Vigneault L. [5 ]
Poirier A. [5 ]
Sanon P.-N. [5 ]
Roch G. [6 ,7 ]
Poitras M.-È. [8 ]
Leblanc A. [1 ,3 ]
Légaré F. [1 ,2 ,3 ]
机构
[1] Centre de recherche sur les soins et services de première ligne de l’Université Laval, CIUSSS de la Capitale-Nationale, Pavillon Landry-Poulin, 2525, chemin de la Canardière, Quebec City, G1J 0A4, QC
[2] Tier 1 Canada Research Chair in Shared Decision Making and Knowledge Translation, Université Laval, Quebec, QC
[3] Department of Family Medicine and Emergency Medicine, Faculty of Medicine, Université Laval, Quebec City, QC
[4] Department of Management, Faculty of Business Administration, Université Laval, Quebec City, QC
[5] Centre Hospitalier Universitaire de Québec – Université Laval Research Centre, Hôpital Saint-François d’Assise, Quebec City, QC
[6] Faculty of Nursing, Université Laval, Quebec City, QC
[7] Department of Health Sciences, Université du Québec à Chicoutimi, Chicoutimi, QC
基金
加拿大健康研究院;
关键词
Participatory action research; Patient advisory council; Patient involvement; Patient-centeredness; Primary care; Quality improvement;
D O I
10.1186/s40900-018-0113-3
中图分类号
学科分类号
摘要
Background Involvement of end-users, including patients, managers and clinicians, in identifying quality improvement and research priorities might improve the relevance of projects and increase their impact. Few patient engagement initiatives have taken place in community based primary care practices (CBPCPs) and best practices for engaging patients in such settings are not well defined. The aim of this pilot study is to develop and assess the feasibility of a new collaborative model of advisory council involving clinicians, managers, patients and caregivers in CBPCP to strengthen their capacity to conduct quality improvement and patient-oriented research projects. Methods We will conduct a participatory action research project in two non-academic CBPCPs in Quebec City (Canada). In each CBPCP, the advisory council will include 12 patients or caregivers, a clinician and a clinic manager. Patients or their caregivers will be identified by clinicians and contacted by patient-experts. They will be eligible if they are registered at the practice, motivated, and available to attend meetings. The council will meet every 6 weeks for a total of six meetings. Two patient-experts will guide council members to identify quality improvement priorities and patient-oriented research questions based on their experience in the clinic. They will then be supported to plan actions to target these priorities. Analysis of meetings will be based on feasibility criteria, notes by non-participant observers in log books, audio-recording of the meetings and questionnaires to evaluate council members’ perceptions and the likelihood they would engage in such councils. Discussion The results of this study will be a model of patient engagement and a discussion of factors to improve the model to fit the needs of primary care patients and professionals. This will lay the foundation for a sustainable structure for long-term patient engagement and contribute to the development of a patient-centered and quality-improvement culture in CBPCPs. © The Author(s) 2018.
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