Mapping the impact of patient and public involvement on health and social care research: a systematic review. (19th July 2012)
- Record Type:
- Journal Article
- Title:
- Mapping the impact of patient and public involvement on health and social care research: a systematic review. (19th July 2012)
- Main Title:
- Mapping the impact of patient and public involvement on health and social care research: a systematic review
- Authors:
- Brett, Jo
Staniszewska, Sophie
Mockford, Carole
Herron‐Marx, Sandra
Hughes, John
Tysall, Colin
Suleman, Rashida - Abstract:
- <abstract abstract-type="main" id="hex795-abs-0001"> <title>Abstract</title> <sec id="hex795-sec-0001" sec-type="section"> <title>Background</title> <p>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.</p> </sec> <sec id="hex795-sec-0002" sec-type="section"> <title>Objective</title> <p>To identify the impact of patient and public involvement on health and social care research.</p> </sec> <sec id="hex795-sec-0003" sec-type="section"> <title>Design</title> <p>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 Centre for Reviews and Dissemination 2009 and the Critical Appraisal Skills Programme (CASP). Grey literature was assessed using the Dixon‐Woods <italic>et al</italic>. (2005) checklist.</p> </sec> <sec id="hex795-sec-0004" sec-type="section"> <title>Inclusion criteria</title> <p>All study types that reported the impact PPI had on the health and/or social care research study.</p> </sec> <sec id="hex795-sec-0005" sec-type="section"> <title>Main results</title> <p>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<abstract abstract-type="main" id="hex795-abs-0001"> <title>Abstract</title> <sec id="hex795-sec-0001" sec-type="section"> <title>Background</title> <p>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.</p> </sec> <sec id="hex795-sec-0002" sec-type="section"> <title>Objective</title> <p>To identify the impact of patient and public involvement on health and social care research.</p> </sec> <sec id="hex795-sec-0003" sec-type="section"> <title>Design</title> <p>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 Centre for Reviews and Dissemination 2009 and the Critical Appraisal Skills Programme (CASP). Grey literature was assessed using the Dixon‐Woods <italic>et al</italic>. (2005) checklist.</p> </sec> <sec id="hex795-sec-0004" sec-type="section"> <title>Inclusion criteria</title> <p>All study types that reported the impact PPI had on the health and/or social care research study.</p> </sec> <sec id="hex795-sec-0005" sec-type="section"> <title>Main results</title> <p>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.</p> </sec> <sec id="hex795-sec-0006" sec-type="section"> <title>Conclusion</title> <p>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.</p> </sec> </abstract> … (more)
- Is Part Of:
- Health expectations. Volume 17:Number 5(2014)
- Journal:
- Health expectations
- Issue:
- Volume 17:Number 5(2014)
- Issue Display:
- Volume 17, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 17
- Issue:
- 5
- Issue Sort Value:
- 2014-0017-0005-0000
- Page Start:
- 637
- Page End:
- 650
- Publication Date:
- 2012-07-19
- Subjects:
- Medical policy -- Periodicals
Public health -- Periodicals
Health planning -- Periodicals
362.105 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=hex ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1369-7625 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/j.1369-7625.2012.00795.x ↗
- Languages:
- English
- ISSNs:
- 1369-6513
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4275.015545
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3804.xml