Between funder requirements and ‘jobbing scientists’: the evolution of patient and public involvement in a mental health biomedical research centre - a qualitative study
Abstract Background In the UK, there has been a strong drive towards patient and public involvement (PPI) in health research. Its benefits include improvements in the quality, relevance and acceptability of research, and empowerment, self-respect and value for service users. Organisational context c...
Main Authors: | Joanne Evans, Stan (Constantina) Papoulias |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2020-04-01
|
Series: | Research Involvement and Engagement |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s40900-020-00185-7 |
Similar Items
-
The Maudsley Biomedical Research Centre (BRC) data linkage service user and carer advisory group: creating and sustaining a successful patient and public involvement group to guide research in a complex area
by: Amelia Jewell, et al.
Published: (2019-06-01) -
Rapid research response to the COVID-19 pandemic: perspectives from a National Institute for Health Biomedical Research Centre
by: Lorna R. Henderson, et al.
Published: (2022-02-01) -
Translating research into action: an international study of the role of research funders
by: Robert K. D. McLean, et al.
Published: (2018-05-01) -
Involvement of general public in biomedical research
by: C S Pramesh, et al.
Published: (2016-01-01) -
User involvement in ageing and health research: a survey of researchers’ and older adults’ perspectives
by: Maya Kylén, et al.
Published: (2022-09-01)