A little more conversation please? Qualitative study of researchers' and patients' interview accounts of training for patient and public involvement in clinical trials
- PMID: 25928689
- PMCID: PMC4410574
- DOI: 10.1186/s13063-015-0667-4
A little more conversation please? Qualitative study of researchers' and patients' interview accounts of training for patient and public involvement in clinical trials
Abstract
Background: Training in patient and public involvement (PPI) is recommended, yet little is known about what training is needed. We explored researchers' and PPI contributors' accounts of PPI activity and training to inform the design of PPI training for both parties.
Methods: We used semi-structured qualitative interviews with researchers (chief investigators and trial managers) and PPI contributors, accessed through a cohort of clinical trials, which had been funded between 2006 and 2010. An analysis of transcripts of audio-recorded interviews drew on the constant comparative method.
Results: We interviewed 31 researchers and 17 PPI contributors from 28 trials. Most researchers could see some value in PPI training for researchers, although just under half had received such training themselves, and some had concerns about the purpose and evidence base for PPI training. PPI contributors were evenly split in their perceptions of whether researchers needed training in PPI. Few PPI contributors had themselves received training for their roles. Many informants across all groups felt that training PPI contributors was unnecessary because they already possessed the skills needed. Informants were also concerned that training would professionalise PPI contributors, limiting their ability to provide an authentic patient perspective. However, informants welcomed informal induction 'conversations' to help contributors understand their roles and support them in voicing their opinions. Informants believed that PPI contributors should be confident, motivated, intelligent, focussed on helping others and have relevant experience. Researchers looked for these qualities when selecting contributors, and spoke of how finding 'the right' contributor was more important than accessing 'the right' training.
Conclusions: While informants were broadly receptive to PPI training for researchers, they expressed considerable reluctance to training PPI contributors. Providers of training will need to address these reservations. Our findings point to the importance of reconsidering how training is conceptualised, designed and promoted and of providing flexible, learning opportunities in ways that flow from researchers' and contributors' needs and preferences. We also identify some areas of training content and the need for further consideration to be given to the selection of PPI contributors and models for implementing PPI to ensure clinical trials benefit from a diversity of patient perspectives.
Figures
Similar articles
-
What Difference Does Patient and Public Involvement Make and What Are Its Pathways to Impact? Qualitative Study of Patients and Researchers from a Cohort of Randomised Clinical Trials.PLoS One. 2015 Jun 8;10(6):e0128817. doi: 10.1371/journal.pone.0128817. eCollection 2015. PLoS One. 2015. PMID: 26053063 Free PMC article.
-
From plans to actions in patient and public involvement: qualitative study of documented plans and the accounts of researchers and patients sampled from a cohort of clinical trials.BMJ Open. 2014 Dec 4;4(12):e006400. doi: 10.1136/bmjopen-2014-006400. BMJ Open. 2014. PMID: 25475243 Free PMC article.
-
An evidence base to optimise methods for involving patient and public contributors in clinical trials: a mixed-methods study.Southampton (UK): NIHR Journals Library; 2015 Sep. Southampton (UK): NIHR Journals Library; 2015 Sep. PMID: 26378330 Free Books & Documents. Review.
-
Patient and public involvement in randomised clinical trials: a mixed-methods study of a clinical trials unit to identify good practice, barriers and facilitators.Trials. 2021 Oct 23;22(1):735. doi: 10.1186/s13063-021-05701-y. Trials. 2021. PMID: 34688304 Free PMC article. Clinical Trial.
-
A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study.Res Involv Engagem. 2023 May 31;9(1):37. doi: 10.1186/s40900-023-00440-7. Res Involv Engagem. 2023. PMID: 37259130 Free PMC article. Review.
Cited by
-
Patient and Public Involvement for Dementia Research in Low- and Middle-Income Countries: Developing Capacity and Capability in South Asia.Front Neurol. 2021 Mar 23;12:637000. doi: 10.3389/fneur.2021.637000. eCollection 2021. Front Neurol. 2021. PMID: 33833728 Free PMC article.
-
A patient and public involvement (PPI) toolkit for meaningful and flexible involvement in clinical trials - a work in progress.Res Involv Engagem. 2016 Apr 27;2:15. doi: 10.1186/s40900-016-0029-8. eCollection 2016. Res Involv Engagem. 2016. PMID: 29062516 Free PMC article.
-
Reflections on qualitative data analysis training for PPI partners and its implementation into practice.Res Involv Engagem. 2019 Aug 14;5:22. doi: 10.1186/s40900-019-0156-0. eCollection 2019. Res Involv Engagem. 2019. PMID: 31428457 Free PMC article.
-
Training and peer-group coaching for pairs of researchers and patient representatives to support continuous two-way learning.Res Involv Engagem. 2024 Oct 25;10(1):110. doi: 10.1186/s40900-024-00646-3. Res Involv Engagem. 2024. PMID: 39456103 Free PMC article.
-
Implementing early rehabilitation and mobilisation for children in UK paediatric intensive care units: the PERMIT feasibility study.Health Technol Assess. 2023 Nov;27(27):1-155. doi: 10.3310/HYRW5688. Health Technol Assess. 2023. PMID: 38063184 Free PMC article.
References
-
- National Health and Medical Research Council and Consumers’ Health Forum of Australia. A Model Framework for Consumer and Community Participation in Health and Medical Research. Canberra: Australian Government; 2005.
-
- Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada, Social Sciences and Humanities Research Council of Canada: Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans. http://www.pre.ethics.gc.ca/pdf/eng/tcps2/TCPS_2_FINAL_Web.pdf. Accessed 28 July 2014.
-
- Department of Health . Best research for best health: a new national health research strategy. London: Department of Health; 2006. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources