Literature DB >> 12940792

Evolving the multiple roles of 'patients' in health-care research: reflections after involvement in a trial of shared decision-making.

Hazel Thornton1, Adrian Edwards, Glyn Elwyn.   

Abstract

OBJECTIVE: This paper offers 'consumer-led' reflections by steering group members of a patient-centred research study involving consumer advocates, patients' associations and patients, throughout the whole study, from pre- to post-study phases. ORIGINAL STUDY
DESIGN: The study: 'Shared decision making and risk communication in general practice' incorporated systematic reviews, psychometric evaluation of outcome measures, and quantitative, qualitative and health economic analyses of a cluster randomized trial of professional skill development, all informed by consumer and patient engagement. SETTING AND PARTICIPANTS: The work was produced by a wide collaboration led by researchers from the Department of General Practice, University of Wales College of Medicine, Cardiff, including a consumers' advisory group and a patients' association. The study participants were 20 general practitioners from Gwent, their practice staff, and almost 800 patients at these practices. DISCUSSION: Consumers and patients contributed to several stages of the research from inception and design, securing of funding, implementation of the protocol, and interpretation and dissemination of the findings. 'Patient involvement' research initiatives that include an equally wide variety of 'user' participants as 'health-professional' participants, accountable to a 'Health in Partnership' funded project, require a user-led viewpoint to be presented and disseminated. This paper presents reflections on the processes of the research, the interpretations of study findings by the involved parties, and notes how this model is fundamental to effective research in the field of patient-centred health care if future practice, policy and research are to change.

Entities:  

Mesh:

Year:  2003        PMID: 12940792      PMCID: PMC5060182          DOI: 10.1046/j.1369-6513.2003.00231.x

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  17 in total

1.  Outcomes that matter to patients in tombstone trials.

Authors:  I Chalmers; M Clarke
Journal:  Lancet       Date:  2001-11-10       Impact factor: 79.321

2.  Recruitment of women into trials.

Authors:  Hazel Thornton; Mary Dixon-Woods
Journal:  Lancet       Date:  2002-01-12       Impact factor: 79.321

Review 3.  Explaining risks: turning numerical data into meaningful pictures.

Authors:  Adrian Edwards; Glyn Elwyn; Al Mulley
Journal:  BMJ       Date:  2002-04-06

4.  Finding a voice.

Authors: 
Journal:  Lancet       Date:  2002-06-08       Impact factor: 79.321

5.  Participating in primary care research.

Authors:  Robert K McKinley; Mary Dixon-Woods; Hazel Thornton
Journal:  Br J Gen Pract       Date:  2002-12       Impact factor: 5.386

6.  Prostate specific antigen testing for prostate cancer.

Authors:  Hazel Thornton; Mary Dixon-Woods
Journal:  BMJ       Date:  2002-10-05

7.  Why men with prostate cancer want wider access to prostate specific antigen testing: qualitative study.

Authors:  Alison Chapple; Sue Ziebland; Sasha Shepperd; Rachel Miller; Andrew Herxheimer; Ann McPherson
Journal:  BMJ       Date:  2002-10-05

Review 8.  Quality improvement report: Improving design and conduct of randomised trials by embedding them in qualitative research: ProtecT (prostate testing for cancer and treatment) study. Commentary: presenting unbiased information to patients can be difficult.

Authors:  Jenny Donovan; Nicola Mills; Monica Smith; Lucy Brindle; Ann Jacoby; Tim Peters; Stephen Frankel; David Neal; Freddie Hamdy
Journal:  BMJ       Date:  2002-10-05

9.  Thrombolysis for acute ischaemic stroke: consumer involvement in design of new randomised controlled trial.

Authors:  Liedeke Koops; Richard I Lindley
Journal:  BMJ       Date:  2002-08-24

10.  The development of COMRADE--a patient-based outcome measure to evaluate the effectiveness of risk communication and treatment decision making in consultations.

Authors:  Adrian Edwards; Glyn Elwyn; Kerry Hood; Michael Robling; Christine Atwell; Margaret Holmes-Rovner; Paul Kinnersley; Helen Houston; Ian Russell
Journal:  Patient Educ Couns       Date:  2003-07
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  15 in total

1.  Patients' understanding of risk.

Authors:  Hazel Thornton
Journal:  BMJ       Date:  2003-09-27

2.  Perceptions around concordance--focus groups and semi-structured interviews conducted with consumers, pharmacists and general practitioners.

Authors:  Jasmina Bajramovic; Lynne Emmerton; Susan E Tett
Journal:  Health Expect       Date:  2004-09       Impact factor: 3.377

Review 3.  Patient empowerment as a component of health system reforms: rights, benefits and vested interests.

Authors:  Cinzia Colombo; Lorenzo Moja; Marien Gonzalez-Lorenzo; Alessandro Liberati; Paola Mosconi
Journal:  Intern Emerg Med       Date:  2012-01-26       Impact factor: 3.397

4.  User involvement in the development of a research bid: barriers, enablers and impacts.

Authors:  Sophie Staniszewska; Nicola Jones; Mary Newburn; Shanit Marshall
Journal:  Health Expect       Date:  2007-06       Impact factor: 3.377

5.  Receiving a summary of the results of a trial: qualitative study of participants' views.

Authors:  Mary Dixon-Woods; Clare Jackson; Kate C Windridge; Sara Kenyon
Journal:  BMJ       Date:  2006-01-09

6.  Participating in a trial in a critical situation: a qualitative study in pregnancy.

Authors:  S Kenyon; M Dixon-Woods; C J Jackson; K Windridge; E Pitchforth
Journal:  Qual Saf Health Care       Date:  2006-04

7.  Developing participatory research in radiology: the use of a graffiti wall, cameras and a video box in a Scottish radiology department.

Authors:  Sandra A Mathers; Helen Anderson; Sheila McDonald; Rosemary A Chesson
Journal:  Pediatr Radiol       Date:  2009-12-01

8.  Participants' preference for type of leaflet used to feed back the results of a randomised trial: a survey.

Authors:  Stephen Brealey; Lazaros Andronis; Laura Dennis; Christine Atwell; Stirling Bryan; Simon Coulton; Helen Cox; Ben Cross; Fiona Fylan; Andrew Garratt; Fiona Gilbert; Maureen Gillan; Maggie Hendry; Kerenza Hood; Helen Houston; David King; Veronica Morton; Michael Robling; Ian Russell; Clare Wilkinson
Journal:  Trials       Date:  2010-12-01       Impact factor: 2.279

Review 9.  Effects of consumers and health providers working in partnership on health services planning, delivery and evaluation.

Authors:  Dianne Lowe; Rebecca Ryan; Lina Schonfeld; Bronwen Merner; Louisa Walsh; Lisa Graham-Wisener; Sophie Hill
Journal:  Cochrane Database Syst Rev       Date:  2021-09-15

10.  Needs-led research: a way of employing user involvement when devising research questions on the trust model in community home-based health care services in Norway.

Authors:  Ruth-Ellen Slåtsveen; Torunn Wibe; Liv Halvorsrud; Anne Lund
Journal:  Res Involv Engagem       Date:  2021-06-22
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