Literature DB >> 15814182

The experiential knowledge of patients: a new resource for biomedical research?

J Francisca Caron-Flinterman1, Jacqueline E W Broerse, Joske F G Bunders.   

Abstract

Both governments and patients' movements are increasingly making a plea in favour of the active participation of patients in biomedical research processes. One of the arguments concerns the contribution that patients could make to the relevance and quality of biomedical research based on their 'experiential knowledge'. This article reflects on the validity of patients' experiential knowledge in the context of biomedical research processes. Since a conclusive argument on the validity of patients' experiential knowledge could not be reached on the basis of theoretical reflection alone, a pragmatic approach was chosen that assessed the validity of patients' experiential knowledge in terms of its practical usefulness for biomedical research. Examples of patient participation in biomedical research were sought through literature research and more than 60 interviews with (bio)medical scientists, patients, representatives from patients' organisations, and health professionals in the Netherlands and the United Kingdom. These examples were analysed for a concrete contribution by patients to the research process. Twenty-one cases of patient participation in biomedical research were identified. After further analysis, concrete use of patients' experiential knowledge could be traced for nine of these cases. These findings suggest that patients' experiential knowledge, when translated into explicit demands, ideas, or judgements, can contribute to the relevance and quality of biomedical research. However, its deliberate use would require a more structural and interactive approach to patient participation. Since the implementation of such an approach could face various obstacles in current biomedical research practices, further research will be needed to investigate its feasibility.

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Year:  2004        PMID: 15814182     DOI: 10.1016/j.socscimed.2004.11.023

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  98 in total

1.  Assessment of the benefits of user involvement in health research from the Warwick Diabetes Care Research User Group: a qualitative case study.

Authors:  Antje Lindenmeyer; Hilary Hearnshaw; Jackie Sturt; Ralph Ormerod; Geoff Aitchison
Journal:  Health Expect       Date:  2007-09       Impact factor: 3.377

2.  Addressing Deficits and Injustices: The Potential Epistemic Contributions of Patients to Research.

Authors:  Katrina Hutchison; Wendy Rogers; Vikki A Entwistle
Journal:  Health Care Anal       Date:  2017-12

Review 3.  Close to the bench as well as at the bedside: involving service users in all phases of translational research.

Authors:  Felicity Callard; Diana Rose; Til Wykes
Journal:  Health Expect       Date:  2011-05-25       Impact factor: 3.377

4.  Knowledge translation in mental health: a scoping review.

Authors:  Elliot M Goldner; Victoria Jeffries; Dan Bilsker; Emily Jenkins; Matthew Menear; Lisa Petermann
Journal:  Healthc Policy       Date:  2011-11

5.  The Potential of the Imitation Game Method in Exploring Healthcare Professionals' Understanding of the Lived Experiences and Practical Challenges of Chronically Ill Patients.

Authors:  Rik Wehrens
Journal:  Health Care Anal       Date:  2015-09

6.  Patients as research partners; how to value their perceptions, contribution and labor?

Authors:  Elise Smith; Jean-Chrisophe Bélisle-Pipon; David Resnik
Journal:  Citiz Sci       Date:  2019-03-08

7.  Practice-based research agenda priorities selected by patients: findings from a dental practice-based research network.

Authors:  Naoki Kakudate; Yoko Yokoyama; Futoshi Sumida; Yuki Matsumoto; Joseph L Riley; Valeria V Gordan; Gregg H Gilbert
Journal:  Int Dent J       Date:  2018-10-23       Impact factor: 2.512

8.  Status, challenges and facilitators of consumer involvement in Australian health and medical research.

Authors:  Carla Saunders; Afaf Girgis
Journal:  Health Res Policy Syst       Date:  2010-11-18

9.  Aiming for inclusion: a case study of motivations for involvement in mental health-care governance by ethnic minority users.

Authors:  Cláudia de Freitas
Journal:  Health Expect       Date:  2013-05-27       Impact factor: 3.377

10.  Patients' experience compared with physicians' recommendations for treating fecal incontinence: a qualitative approach.

Authors:  Sara B Cichowski; Gena C Dunivan; Rebecca G Rogers; Yuko M Komesu
Journal:  Int Urogynecol J       Date:  2014-02-27       Impact factor: 2.894

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