Literature DB >> 19691463

What is involvement in research and what does it achieve? Reflections on a pilot study of the personal costs of stroke.

Christopher McKevitt1, Nina Fudge, Charles Wolfe.   

Abstract

BACKGROUND: Health researchers are encouraged to involve service users as partners in their research. There is a need to increase the evidence base of involvement, including an accumulation of empirical accounts of involvement practices, demonstrating how involvement influences research and refinement of the concept itself. AIMS: To report the development of a pilot study by academic researchers and stroke service users belonging to a user research group to investigate costs of stroke to individuals and families; to reflect on what this example of user involvement achieved and implications for what involvement means.
METHODS: We conducted a 2-year ethnographic study that included participant observation, formal and informal interviews with professionals and user group members and documentary analysis. Data were systematically recorded to permit description of processes and reflexive analysis. RESULTS AND
CONCLUSIONS: We report on five stages of the research process from service user identification of a research question to interpretation of pilot study findings. Professional researchers led the research process and developed a novel method to involve stroke service users in the development of a questionnaire. Some academic colleagues questioned the value of the proposed investigation as it did not appear to conform to implicit criteria of quality research. We argue that the moral status that user involvement has acquired means that academics' concerns about quality did not prevent the pilot study from being conducted. We suggest that much of what was undertaken might be considered standard good practice in developing new research studies but also identify additional benefits of user involvement. Implications for conceptual development and evaluation are discussed.

Entities:  

Mesh:

Year:  2009        PMID: 19691463      PMCID: PMC5060514          DOI: 10.1111/j.1369-7625.2009.00573.x

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


  20 in total

1.  Ethnography and health care.

Authors:  J Savage
Journal:  BMJ       Date:  2000-12-02

Review 2.  Consumer involvement in health research: a review and research agenda.

Authors:  Jonathan Boote; Rosemary Telford; Cindy Cooper
Journal:  Health Policy       Date:  2002-08       Impact factor: 2.980

3.  Researching sexual and reproductive behaviour: a peer ethnographic approach.

Authors:  Neil Price; Kirstan Hawkins
Journal:  Soc Sci Med       Date:  2002-10       Impact factor: 4.634

4.  Social movements in health: an introduction.

Authors:  Phil Brown; Stephen Zavestoski
Journal:  Sociol Health Illn       Date:  2004-09

5.  Best research for best health: a new national health research strategy.

Authors:  Timothy W Evans
Journal:  Clin Med (Lond)       Date:  2006 Sep-Oct       Impact factor: 2.659

6.  The effect of involvement in participatory research on parent researchers in a Sure Start programme.

Authors:  Ann Rowe
Journal:  Health Soc Care Community       Date:  2006-11

7.  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

8.  What patients want: consumer involvement in the design of a randomized controlled trial of routine oxygen supplementation after acute stroke.

Authors:  Khalid Ali; Christine Roffe; Peter Crome
Journal:  Stroke       Date:  2006-02-02       Impact factor: 7.914

9.  Consumers leading public consultation: the general public's knowledge of stroke.

Authors:  Laura J Morgan; Ruth Chambers; Jyoti Banerji; John Gater; Joanne Jordan
Journal:  Fam Pract       Date:  2005-01-07       Impact factor: 2.267

10.  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
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  11 in total

1.  Consumer involvement in systematic reviews of comparative effectiveness research.

Authors:  Julia Kreis; Milo A Puhan; Holger J Schünemann; Kay Dickersin
Journal:  Health Expect       Date:  2012-03-06       Impact factor: 3.377

2.  Involving service users in intervention design: a participatory approach to developing a text-messaging intervention to reduce repetition of self-harm.

Authors:  Christabel Owens; Paul Farrand; Ruth Darvill; Tobit Emmens; Elaine Hewis; Peter Aitken
Journal:  Health Expect       Date:  2010-09-23       Impact factor: 3.377

Review 3.  Patient and service user engagement in research: a systematic review and synthesized framework.

Authors:  Nathan D Shippee; Juan Pablo Domecq Garces; Gabriela J Prutsky Lopez; Zhen Wang; Tarig A Elraiyah; Mohammed Nabhan; Juan P Brito; Kasey Boehmer; Rim Hasan; Belal Firwana; Patricia J Erwin; Victor M Montori; M Hassan Murad
Journal:  Health Expect       Date:  2013-06-03       Impact factor: 3.377

4.  Shaping innovations in long-term care for stroke survivors with multimorbidity through stakeholder engagement.

Authors:  Euan Sadler; Talya Porat; Iain Marshall; Uy Hoang; Vasa Curcin; Charles D A Wolfe; Christopher McKevitt
Journal:  PLoS One       Date:  2017-05-05       Impact factor: 3.240

Review 5.  Giving voice to older adults living with frailty and their family caregivers: engagement of older adults living with frailty in research, health care decision making, and in health policy.

Authors:  Jayna Holroyd-Leduc; Joyce Resin; Lisa Ashley; Doris Barwich; Jacobi Elliott; Paul Huras; France Légaré; Megan Mahoney; Alies Maybee; Heather McNeil; Daryl Pullman; Richard Sawatzky; Paul Stolee; John Muscedere
Journal:  Res Involv Engagem       Date:  2016-06-17

6.  Public involvement in health and social sciences research: A concept analysis.

Authors:  Mel Hughes; Catherine Duffy
Journal:  Health Expect       Date:  2018-08-29       Impact factor: 3.377

Review 7.  Evaluating the "return on patient engagement initiatives" in medicines research and development: A literature review.

Authors:  Lidewij Eva Vat; Teresa Finlay; Tjerk Jan Schuitmaker-Warnaar; Nick Fahy; Paul Robinson; Mathieu Boudes; Ana Diaz; Elisa Ferrer; Virginie Hivert; Gabor Purman; Marie-Laure Kürzinger; Robert A Kroes; Claudia Hey; Jacqueline E W Broerse
Journal:  Health Expect       Date:  2019-09-06       Impact factor: 3.377

8.  The Possibilities and Limits of "Co-producing" Research.

Authors:  Jonathan Paylor; Christopher McKevitt
Journal:  Front Sociol       Date:  2019-04-05

9.  Patient and public involvement in stroke research: a scoping review protocol.

Authors:  Patricia Hall; Thilo Kroll; Julianne Hickey; Diarmuid Stokes; Olive Lennon
Journal:  HRB Open Res       Date:  2022-07-28

10.  Conducting research in psoriatic arthritis: the emerging role of patient research partners.

Authors:  Niti Goel
Journal:  Rheumatology (Oxford)       Date:  2020-03-01       Impact factor: 7.580

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