Literature DB >> 36273206

Patient and public involvement in an international rheumatology translational research project: an evaluation.

Savia de Souza1, Eva C Johansson2, Susanne Karlfeldt3, Karim Raza4, Ruth Williams5.   

Abstract

BACKGROUND: Rheuma Tolerance for Cure (RTCure) is a five-year international collaboration between academia, industry and patients/members of the public. It focuses on developing approaches to predict the onset of rheumatoid arthritis (RA) and designing clinical trials to reduce the risk of disease development through immune-tolerising and other treatments. We conducted a mid-term evaluation of patient and public involvement (PPI) within the project.
METHODS: Two surveys on PPI were co-designed by the PPI Coordinator, Patient/Public Research Partners (PRPs) and a researcher. Both anonymous, electronic surveys were distributed to 61 researchers and 9 PRPs. Quantitative survey data were analysed using descriptive statistics and free text responses underwent inductive thematic analysis.
RESULTS: Researcher and Patient response rates were 33% and 78%, respectively. Quantitative Researcher Survey data highlighted that (i) responding researchers represented all seven Work Packages (WPs), (ii) 40% thought PRPs had made a large or extremely large contribution to their own WPs, (iii) 55% thought PPI has had a moderate or large impact on RTCure, (iv) 75% worked with PRPs in RTCure, and (v) 60% said PRPs had affected their research thinking. Quantitative PRP Survey data highlighted that (i) PRPs were most involved in four WPs, (ii) 43% thought they had made a minor contribution to their main WP, (iii) 57% thought PPI has had a small impact on RTCure, and (iv) 57% thought they received too little feedback on the outcome of their contribution to different tasks. Four main themes were identified in both surveys: 'PRP contributions', 'Experiences of PPI', 'Impact of PPI on RTCure', and 'How PPI can be improved'. Two additional themes from the Researcher Survey were 'Impact of PPI on researchers' and 'Influence on Future Projects', and from the PRP Survey were 'Impact of PPI on PRPs' and 'Engagement with PRPs'.
CONCLUSION: PPI seemed to have a significant impact on RTCure, however, PRPs were less aware. A focus on improving communication between PRPs and researchers (facilitated by the PPI Coordinator), and providing PPI training for researchers is likely to improve involvement. Complex legal agreements for PRPs should be avoided and careful attention paid to appropriate PRP compensation.
© 2022. The Author(s).

Entities:  

Keywords:  Clinical trials; Evaluation; Patient and public involvement; Patient engagement; Rheumatoid arthritis; Surveys; Translational research

Year:  2022        PMID: 36273206     DOI: 10.1186/s41927-022-00311-w

Source DB:  PubMed          Journal:  BMC Rheumatol        ISSN: 2520-1026


  22 in total

1.  Implementing a patient-led service for chronic conditions.

Authors:  Denise Pope; Sue Tipler; John Kirwan; Sarah Hewlett
Journal:  Nurs Times       Date:  2005 Dec 6-12

2.  Commentary: Patients as Partners: Building on the Experience of Outcome Measures in Rheumatology.

Authors:  John R Kirwan; Maarten P T de Wit; Clifton O Bingham; Amye Leong; Pamela Richards; Peter Tugwell; Marieke Voshaar; Laure Gossec
Journal:  Arthritis Rheumatol       Date:  2016-06       Impact factor: 10.995

Review 3.  The impact of patient and public involvement on UK NHS health care: a systematic review.

Authors:  Carole Mockford; Sophie Staniszewska; Frances Griffiths; Sandra Herron-Marx
Journal:  Int J Qual Health Care       Date:  2011-11-22       Impact factor: 2.038

4.  Development and initial cohort validation of the Arthritis Research UK Musculoskeletal Health Questionnaire (MSK-HQ) for use across musculoskeletal care pathways.

Authors:  Jonathan C Hill; Sujin Kang; Elena Benedetto; Helen Myers; Steven Blackburn; Stephanie Smith; Kate M Dunn; Elaine Hay; Jonathan Rees; David Beard; Sion Glyn-Jones; Karen Barker; Benjamin Ellis; Ray Fitzpatrick; Andrew Price
Journal:  BMJ Open       Date:  2016-08-05       Impact factor: 2.692

5.  Patient involvement in the development of a handbook for moderate rheumatoid arthritis.

Authors:  Louise Prothero; Sofia Georgopoulou; Savia de Souza; Ailsa Bosworth; Lindsay Bearne; Heidi Lempp
Journal:  Health Expect       Date:  2016-04-18       Impact factor: 3.377

6.  The extent, quality and impact of patient and public involvement in primary care research: a mixed methods study.

Authors:  Steven Blackburn; Sarah McLachlan; Sue Jowett; Philip Kinghorn; Paramjit Gill; Adele Higginbottom; Carol Rhodes; Fiona Stevenson; Clare Jinks
Journal:  Res Involv Engagem       Date:  2018-05-24

7.  Reducing arthritis fatigue impact: two-year randomised controlled trial of cognitive behavioural approaches by rheumatology teams (RAFT).

Authors:  Sarah Hewlett; Celia Almeida; Nicholas Ambler; Peter S Blair; Ernest H Choy; Emma Dures; Alison Hammond; William Hollingworth; Bryar Kadir; John Richard Kirwan; Zoe Plummer; Clive Rooke; Joanna Thorn; Nicholas Turner; Jon Pollock
Journal:  Ann Rheum Dis       Date:  2019-02-06       Impact factor: 19.103

8.  Intensive management for moderate rheumatoid arthritis: a qualitative study of patients' and practitioners' views.

Authors:  Louise Prothero; Jackie Sturt; Savia de Souza; Heidi Lempp
Journal:  BMC Rheumatol       Date:  2019-03-28

9.  Patient and clinician views on the quality of foot health care for rheumatoid arthritis outpatients: a mixed methods service evaluation.

Authors:  Savia de Souza; Ruth Williams; Heidi Lempp
Journal:  J Foot Ankle Res       Date:  2016-01-06       Impact factor: 2.303

10.  Patient involvement in rheumatology outpatient service design and delivery: a case study.

Authors:  Savia de Souza; James Galloway; Carol Simpson; Radka Chura; Joanne Dobson; Nicola J Gullick; Sophia Steer; Heidi Lempp
Journal:  Health Expect       Date:  2016-06-27       Impact factor: 3.377

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