How can we describe impact of adult patient participation in health-service development? A scoping review
Olsson, Ann Britt Sandvin; Strøm, Anita; Haaland-Øverby, Mette; Fredriksen, Kari-Elise; Stenberg, Una
Peer reviewed, Journal article
Published version

View/ Open
Date
2020Metadata
Show full item recordCollections
- Artikler / Articles [1287]
- Publikasjoner fra CRIStin [1248]
Original version
Patient Education and Counseling. 2020, 103 (8), 1453-1466 10.1016/j.pec.2020.02.028Abstract
Objective: Patient participation represents a worldwide policy, but its impact lacks research. This study investigates impact of patient participation in health-service development by providing a comprehensive overview of how the literature describes it.
Method: A scoping review with a broad search strategy was conducted. The literature was examined for study characteristics, purpose for, approaches to and impact of patient participation. The data were analyzed using a thematic analysis.
Results: The 34 included primary studies reported impacts of patient participation that were interpreted to constitute two categories: 1. The participatory process impact on involved patient representatives and health professionals, and the organization s patient participation practice itself. 2. The participatory service development s impact on the design and delivery of services regarding patients and health professionals, and the organization.
Conclusion: The literature describes a broad variation of impacts from health-service development, relevant for health professionals and patient representatives when initiating or participating in such processes. Our review provides an overview and discussion of these types of impact.
Practice implications: The findings can be of practical relevance to those aiming to develop services, quality indicators regarding effects of patient participation, or to further investigate aspects of participatory service development.
Description
This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Publisher
ElsevierJournal
Patient Education and CounselingCopyright
© 2020 The Author(s). Published by Elsevier B.V.Related items
Showing items related by title, author, creator and subject.
-
Immigrant health status and access to healthcare: The case of Norway
Chance, Emmanuel Aoudi (Doctoral thesis, 2018)Health is one of the most important assets of a society; it is necessary for social and economic development and for achieving ample length and quality of life for its members. This thesis asserts that health should be a ... -
Evaluation of the Rosa Chatbot Providing Genetic Information to patients at risk of hereditary breast and ovarian cancer: Qualitative interview study
Siglen, Elen; Vetti, Hildegunn Høberg; Augestad, Mirjam Tonheim; Steen, Vidar Martin; Lunde, Åshild; Bjorvatn, Cathrine (Peer reviewed; Journal article, 2023)Background: Genetic testing has become an integrated part of health care for patients with breast or ovarian cancer, and the increasing demand for genetic testing is accompanied by an increasing need for easy access to ... -
Postnatal depression is a Public Health nursing issue: perspectives from Norway and Ireland
Glavin, Kari; Leahy-Warren, Patricia (Peer reviewed; Journal article, 2013)The framework provided by the Millennium Development Goals includes maternal health as an area of priority. Postnatal depression (PND) is a serious public health issue because it occurs at a crucial time in a mothers’ life, ...