Literature DB >> 18515813

The impact of consumer involvement in research: an evaluation of consumer involvement in the London Primary Care Studies Programme.

Katrina Wyatt1, Mary Carter, Vinita Mahtani, Angela Barnard, Annie Hawton, Nicky Britten.   

Abstract

BACKGROUND: The value of consumer involvement in health services research is widely recognized. While there is a growing body of evidence about the principles of good consumer involvement, there is little research about the effect that involvement can have on the research. This evaluation assessed the level and impact of consumer involvement in the London Primary Care Studies Programme (LPCSP), all of whose individual projects had to demonstrate substantial involvement as a condition of funding.
OBJECTIVE: To evaluate consumer involvement in the LPSCP and understand what impact consumers had on the research process and outcomes.
METHODS: A multi-method case study approach was undertaken, using survey techniques, interviews, focus groups, observation and scrutiny of written documents. The overall data set comprised 61 questionnaires, 44 semi-structured interviews, 2 focus groups and 15 hours of observation of meetings. Eleven primary care-based research projects which together made up the LPCSP.
RESULTS: An in-depth description of consumer involvement in the Programme was produced. Nine projects had consumers as co-applicants, four projects had been completed before the evaluation began and one was still ongoing at the time of the evaluation. Of the eight projects which have produced final reports, all met their aims and objectives. Consumers had had an additional impact in the research, in the initial design of the study, in recruitment of the research subjects, in developing data collection tools, in collecting the data, in analysis and disseminating the findings.
CONCLUSIONS: Consumer involvement in National Health Service research is a relatively recent policy development and while there is an increasing amount of literature about how and why consumers should be involved in research, there is less evidence about the impact of such involvement. This evaluation provides evidence about the impact that consumers have not only on the research process but also on the outcomes of the research.

Mesh:

Year:  2008        PMID: 18515813     DOI: 10.1093/fampra/cmn019

Source DB:  PubMed          Journal:  Fam Pract        ISSN: 0263-2136            Impact factor:   2.267


  19 in total

1.  Can the impact of public involvement on research be evaluated? A mixed methods study.

Authors:  Rosemary Barber; Jonathan D Boote; Glenys D Parry; Cindy L Cooper; Philippa Yeeles; Sarah Cook
Journal:  Health Expect       Date:  2011-02-17       Impact factor: 3.377

2.  Patient and public involvement in patient-reported outcome measures: evolution not revolution.

Authors:  Sophie Staniszewska; Kirstie L Haywood; Jo Brett; Liz Tutton
Journal:  Patient       Date:  2012       Impact factor: 3.883

Review 3.  Mapping the impact of patient and public involvement on health and social care research: a systematic review.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Health Expect       Date:  2012-07-19       Impact factor: 3.377

4.  Patient, Family, and Community Advisory Councils in Health Care and Research: a Systematic Review.

Authors:  Benjamin J Oldfield; Marcus A Harrison; Inginia Genao; Ann T Greene; Mary Ellen Pappas; Janis G Glover; Marjorie S Rosenthal
Journal:  J Gen Intern Med       Date:  2018-07-26       Impact factor: 5.128

5.  Development of the MASCC Teaching Tool for Patients Receiving Oral Agents for Cancer.

Authors:  Sultan Kav; Lisa Schulmeister; Anita Nirenberg; Linda Barber; Judi Johnson; Cynthia Rittenberg
Journal:  Support Care Cancer       Date:  2009-07-10       Impact factor: 3.603

6.  Involving consumers successfully in NHS research: a national survey.

Authors:  Rosemary Barber; Jonathan D Boote; Cindy L Cooper
Journal:  Health Expect       Date:  2007-12       Impact factor: 3.377

Review 7.  A systematic review of the impact of patient and public involvement on service users, researchers and communities.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Patient       Date:  2014       Impact factor: 3.883

8.  Patient Involvement in the Design of a Patient-Centered Clinical Trial to Promote Adherence to Supplemental Oxygen Therapy in COPD.

Authors:  Kristen E Holm; Richard Casaburi; Scott Cerreta; Hélène A Gussin; Julian Husbands; Janos Porszasz; Valentin Prieto-Centurion; Robert A Sandhaus; Jamie L Sullivan; Linda J Walsh; Jerry A Krishnan
Journal:  Patient       Date:  2016-06       Impact factor: 3.883

9.  Assessing public perception of a sand fly biting study on the pathway to a controlled human infection model for cutaneous leishmaniasis.

Authors:  Vivak Parkash; Georgina Jones; Nina Martin; Morgan Steigmann; Elizabeth Greensted; Paul Kaye; Alison M Layton; Charles J Lacey
Journal:  Res Involv Engagem       Date:  2021-05-30

10.  Developing and evaluating a model of public involvement and engagement embedded in a national longitudinal study: HealthWise Wales.

Authors:  Julia Townson; Jan Davies; Lisa Hurt; Pauline Ashfield-Watt; Shantini Paranjothy
Journal:  Int J Popul Data Sci       Date:  2020-04-16
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