Cited by 1,598Mental Health and Patient InvolvementCommunity Health and DevelopmentHealth Policy Implementation Science

The DOI matches its Crossref record; 70 of the 71 references it cites were found in a registry or an index.

Mapping the impact of patient and public involvement on health and social care research: a systematic review

Open access
Brett, Jo, Staniszewska, Sophie, Mockford, Carole, Herron‐Marx, Sandra, Hughes, John, Tysall, Colin, Suleman, Rashida·2014·Health Expectations

Abstract

Background: There is an increasing international interest in patient and public involvement ( PPI ) in research, yet relatively little robust evidence exists about its impact on health and social care research. Objective: To identify the impact of patient and public involvement on health and social care research. Design: A systematic search of electronic databases and health libraries was undertaken from 1995 to 2009. Data were extracted and quality assessed utilizing the guidelines of the NHS C entre for R eviews and D issemination 2009 and the C ritical A ppraisal S kills P rogramme ( CASP ). Grey literature was assessed using the D ixon‐ W oods et al . (2005) checklist. Inclusion criteria: All study types that reported the impact PPI had on the health and/or social care research study. Main results: A total of 66 studies reporting the impact of PPI on health and social care research were included. The positive impacts identified enhanced the quality and appropriateness of research. Impacts were reported for all stages of research, including the development of user‐focused research objectives, development of user‐relevant research questions, development of user‐friendly information, questionnaires and interview schedules, more appropriate recruitment strategies for studies, consumer‐focused interpretation of data and enhanced implementation and dissemination of study results. Some challenging impacts were also identified. Conclusion: This study provides the first international evidence of PPI impact that has emerged at all key stages of the research process. However, much of the evidence base concerning impact remains weak and needs significant enhancement in the next decade.

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Crossref · 10.1111/j.1369-7625.2012.00795.x

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Show all 71 references

Research works printed but not linked: 12

  1. Dixon P, 1999, A Database of Examples of Consumer Involvement in Research
  2. Blaxter M, 1995, Consumer Issues Within the NHS: An R & D Contribution to Consumer Involvement in the NHS
  3. Brett J, 2010, Systematic Review of the Conceptualization, Measurement, Impact and Outcomes of Patient and Public Involvement in Health and Social Care Research
  4. Dixon‐Woods M, 2005, Vulnerable Groups and Access, to Health Care: A Critical Interpretative Review
  5. Popay J, 2005, Developing guidance on conduct of narrative synthesis in systematic reviews, Journal of Epidemiology and Community Health, 59, A7
  6. UKCRC & TwoCan Associates, 2009, An Evaluation of the Process and Impact of Patient and Public Involvement in the Advisory Groups of the UK Clinical Research Collaboration
  7. Faulkner A, 2006, Beyond our Expectations: A Report of the Experiences of Involving Service Users in Forensic Mental Health Research
  8. Sainsbury Centre for Mental Health, 2008, A Review of Service User Involvement in Prison Mental Health Research
  9. Kelson M, 1999, National Sentinel Audits Involving Older People: A Guide to Involving Older People in Local Audit Activity
  10. 10.1080/13561820400011792 · DOI
  11. Rose D, 2004, Telling different stories: user involvement in mental health research, Research and Policy Planning, 22, 23
  12. Faulkner A, 2004, Capturing the Experiences of those Involved in the TRUE Project. A Story of Colliding Worlds

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Metadata

Authors
Brett, J., Staniszewska, S., Mockford, C., Herron‐Marx, S., Hughes, J., Tysall, C., & Suleman, R.
Affiliations
  • University of Warwick (GB)
  • Royal College of Nursing Research Institute, School of Health and Social Studies, University of Warwick Coventry UK
  • United Kingdom Clinical Research Collaboration (GB)
Corresponding author
Brett, Jo
Venue
Health Expectations
Publisher
Wiley
Published
2012-07-19
Volume
17
Issue
5
Pages
637-650
ISSN
  • 1369-6513 (ISSN-L)
  • 1369-7625
OpenAlex
W2049504028
Cited by
1,598
References
71
Citations by year
2026: 140 · 2025: 167 · 2024: 201 · 2023: 171 · 2022: 151 · 2021: 154 · 2020: 158 · 2019: 133 · 2018: 119 · 2017: 78 · 2016: 55 · 2015: 39 · 2014: 15 · 2013: 16
FWCI
3.41
Type
journal article
Language
en
Open access
Locations
  • Health Expectations (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Open Research Online - ORO (The Open University) (submittedVersion)
Funders
  • London School of Hygiene and Tropical Medicine
  • United Kingdom Clinical Research Collaboration
  • University of Warwick
Topics
  • Health Sciences › Health Professions › General Health Professions › Mental Health and Patient Involvement
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Community Health and Development
  • Health Sciences › Health Professions › General Health Professions › Health Policy Implementation Science
Keywords
patient and public involvement, health research, social care research, research quality, research questions, research recruitment, research dissemination, implementation of research findings, research stages
MeSH terms
Health Services Research, Humans, Patient Participation, Social Welfare, Community-Based Participatory Research

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