Literature DB >> 27633160

A synthesis of the evidence on peer research with potentially vulnerable adults: how this relates to dementia.

Claudio Di Lorito1, Linda Birt2, Fiona Poland2, Emese Csipke3, Dianne Gove4, Ana Diaz-Ponce4, Martin Orrell1.   

Abstract

BACKGROUND: There is limited literature around peer research in dementia. This study aims to identify the benefits, the risks and the practical challenges and to develop a model of good practice in peer research with people with dementia.
METHODS: We searched on PsycInfo, PubMed and Google Scholar for empirical investigations or discussion papers on peer research. Given the limited literature in the field of dementia, we included studies with groups who share similar demographics (older people), experience of stigma (mental health service users) and exclusion from research (people with learning disabilities). We applied no restrictions on language and publication date. ANALYSIS: We identified three themes: the potential benefits, the potential risks and the practical challenges of peer research. We developed a model of good practice. The European Working Group of People with Dementia reviewed our paper and added to our findings.
RESULTS: We included seven papers. Potential benefits of peer research included enriched data and empowering people with dementia. Potential risks included power differentials between researchers and issues of representativeness. The practical issues for good practice included the training of peer researchers, defining involvement and roles, working with cognitive impairment and considering resource implications. The European Working Group of People with Dementia emphasised the importance of equality issues.
CONCLUSION: Involving people with dementia in peer research can generate several benefits, including empowerment and opportunities for inclusion for the peer researchers and the research participants living with dementia, challenging academics' traditional views on research processes and gathering enhanced research data. There remains a need for further research on the impact of peer research in dementia studies.
Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

Entities:  

Keywords:  co-research; dementia; participatory research; patient and public involvement; peer research

Mesh:

Year:  2016        PMID: 27633160     DOI: 10.1002/gps.4577

Source DB:  PubMed          Journal:  Int J Geriatr Psychiatry        ISSN: 0885-6230            Impact factor:   3.485


  11 in total

1.  Planning Ahead for Dementia Research Participation: Insights from a Survey of Older Australians and Implications for Ethics, Law and Practice.

Authors:  Nola Ries; Elise Mansfield; Rob Sanson-Fisher
Journal:  J Bioeth Inq       Date:  2019-07-11       Impact factor: 1.352

Review 2.  A review of reviews on principles, strategies, outcomes and impacts of research partnerships approaches: a first step in synthesising the research partnership literature.

Authors:  F Hoekstra; K J Mrklas; M Khan; R C McKay; M Vis-Dunbar; K M Sibley; T Nguyen; I D Graham; H L Gainforth
Journal:  Health Res Policy Syst       Date:  2020-05-25

3.  Co-producing a shared understanding and definition of empowerment with people with dementia.

Authors:  Tracey McConnell; Tristan Sturm; Mabel Stevenson; Noleen McCorry; Michael Donnelly; Brian J Taylor; Paul Best
Journal:  Res Involv Engagem       Date:  2019-06-10

4.  Embedding patient and public involvement: Managing tacit and explicit expectations.

Authors:  Fiona Poland; Georgina Charlesworth; Phuong Leung; Linda Birt
Journal:  Health Expect       Date:  2019-09-20       Impact factor: 3.377

Review 5.  Ethical considerations for engaging frail and seriously ill patients as partners in research: sub-analysis of a systematic review.

Authors:  Claire Ludwig; Ian D Graham; Josee Lavoie; Wendy Gifford; Dawn Stacey
Journal:  Res Involv Engagem       Date:  2021-01-31

6.  A Case Study of Co-production Within a Mental Health Recovery College Dementia Course: Perspectives of A Person With Dementia, Their Family Supporter and Mental Health Staff.

Authors:  Juniper West; Linda Birt; Danielle Wilson; Elspeth Mathie; Fiona Poland
Journal:  Front Rehabil Sci       Date:  2022-06-22

7.  Adding to the knowledge on Patient and Public Involvement: Reflections from an experience of co-research with carers of people with dementia.

Authors:  Claudio Di Lorito; Maureen Godfrey; Marianne Dunlop; Alessandro Bosco; Kristian Pollock; Veronika van der Wardt; Rowan H Harwood
Journal:  Health Expect       Date:  2020-03-17       Impact factor: 3.377

8.  Use of nonintrusive sensor-based information and communication technology for real-world evidence for clinical trials in dementia.

Authors:  Stefan Teipel; Alexandra König; Jesse Hoey; Jeff Kaye; Frank Krüger; Julie M Robillard; Thomas Kirste; Claudio Babiloni
Journal:  Alzheimers Dement       Date:  2018-06-21       Impact factor: 21.566

9.  Working with Aboriginal young people in sexual health research: a peer research methodology in remote Australia.

Authors:  Stephen Bell; Peter Aggleton; Andrew Lockyer; Tellisa Ferguson; Walbira Murray; Bronwyn Silver; John Kaldor; Lisa Maher; James Ward
Journal:  Qual Health Res       Date:  2020-10-03

Review 10.  Public Engagement and Neurology: An Update.

Authors:  Luigi Lavorgna; Francesco Brigo; Sabrina Esposito; Gianmarco Abbadessa; Maddalena Sparaco; Roberta Lanzillo; Marcello Moccia; Matilde Inglese; Luca Bonfanti; Francesca Trojsi; Emanuele Spina; Antonio Russo; Pasquale De Micco; Marinella Clerico; Gioacchino Tedeschi; Simona Bonavita
Journal:  Brain Sci       Date:  2021-03-28
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