Rosemary Barber

Dados Biográficos

ID207974
NOMERosemary Barber
PRENOMESRosemary
SOBRENOMEBarber
ASSINATURABARBER R
AFILIAÇÕESUniversity of Sheffield
ORCID0000-0003-1981-7830
VERIFICADOSim
TOTAL DE OBRAS9
TOTAL DE CITAÇÕES27
TOTAL COMO AUTOR9
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO2007
ANO MAIS RECENTE DE PUBLICAÇÃO2018
ÍNDICE H3

  • Integrating Qualitative and Quantitative Data in the Development of Outcome Measures

    Open AccessAnju Keetharuth, Elizabeth Taylor Buck et al.ARTICLEInternational Journal of…2018

    While it is important to treat symptoms, there is growing recognition that in order to help people with mental health problems lead meaningful and fulfilling lives, it is crucial to capture the impact of their conditions on wider aspects of their social lives. We constructed two versions of the Recovering Quality of Life (ReQoL) measure—ReQoL-10 and ReQoL-20—for use in routine settings and clinical trials from a larger pool of items by combining …

  • GRIPP2 reporting checklists

    Open AccessSophie Staniszewska, Jo Brett et al.ARTICLEResearch Involvement and Engagement2017

    While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research partners at all stages…

  • GRIPP2 reporting checklists

    Open AccessSophie Staniszewska, Jo Brett et al.ARTICLEBMJ2017

    Background While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. Objective To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research p…

  • Exploring the Impact of Patient and Public Involvement in a Cancer Research Setting

    Open AccessJill Thompson, Paul Bissell et al.ARTICLEQualitative Health Research2014Citada por: 4Referências: 19

    An enduring theme in the literature exploring patient and public involvement (PPI) in research has been the focus on evaluating impact, defined usually in terms of participants' practical contribution to enhancing research processes. By contrast, there has been less emphasis on the perspectives and experiences of those involved in PPI. Drawing on qualitative data with people involved in the National Cancer Research Network in the United Kingdom, …

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

    Open AccessRosemary Barber, Jonathan D Boote et al.ARTICLEHealth Expectations2012

    Background Public involvement is central to health and social research policies, yet few systematic evaluations of its impact have been carried out, raising questions about the feasibility of evaluating the impact of public involvement. Objective To investigate whether it is feasible to evaluate the impact of public involvement on health and social research. Methods Mixed methods including a two‐round Delphi study with pre‐specified 80% consensus…

  • Credibility and the 'professionalized' lay expert

    Open AccessJill Thompson, Paul Bissell et al.ARTICLEHealth An Interdisciplinary…2012Citada por: 15Referências: 13

    Contemporary health policy in England places increasing emphasis on patient and public involvement (PPI) in health and health research. With regard to the latter, it has been suggested that PPI brings 'different' perspectives to research decision-making spaces, based on what has been referred to as 'experiential expertise'. This article presents findings from a qualitative study of PPI in cancer research settings in England. We argue that partici…

  • Critical perspectives on 'consumer involvement' in health research

    Open AccessP Ward, Paul R Ward et al.ARTICLEJournal of Sociology2010Citada por: 8Referências: 33

    Researchers in the area of health and social care (both in Australia and internationally) are encouraged to involve consumers throughout the research process, often on ethical, political and methodological grounds, or simply as 'good practice'. This article presents findings from a qualitative study in the UK of researchers' experiences and views of consumer involvement in health research. Two main themes are presented. First, we explore the 'kno…

  • Health researchers’ attitudes towards public involvement in health research

    Open AccessJill Thompson, Rosemary Barber et al.ARTICLEHealth Expectations2009

    Objective To investigate health researchers’ attitudes to involving the public in research. Background Public involvement in research is encouraged by the Department of Health in the UK. Despite this, the number of health researchers actively involving the public in research appears to be limited. There is little research specifically addressing the attitudes of health researchers towards involving the public: how they interpret the policy, what …

  • Involving consumers successfully in NHS research

    Open AccessRosemary Barber, Jonathan D Boote et al.ARTICLEHealth Expectations2007

    Objectives To investigate how far and in what way consumers are involved in NHS research. Background There is guidance from the UK Department of Health on involving consumers in research, but it is not known how these policies have been implemented. Design A national postal survey was conducted of 884 researchers selected randomly from the National Research Register, 16 researchers registered on the INVOLVE database and 15 consumers nominated by …