Patients as research partners in preference studies: learnings from IMI-PREFER
- PMID: 37029449
- PMCID: PMC10080166
- DOI: 10.1186/s40900-023-00430-9
Patients as research partners in preference studies: learnings from IMI-PREFER
Abstract
Background: There is growing recognition of the importance of patient and public stakeholder involvement (PPI) in patient preference research. However, limited evidence exists regarding the impact, barriers and enablers of PPI in preference studies. The Innovative Medicines Initiative (IMI)-PREFER project conducted a series of preference case studies which incorporated PPI.
Objective: To describe: (1) how PPI was operationalized in the PREFER case studies, (2) the impact of PPI, and (3) factors that served to impede and facilitate PPI.
Methods: We reviewed the PREFER final study reports to determine how patient partners were involved. We conducted a thematic framework analysis to characterize the impact of PPI and then administered a questionnaire to the PREFER study leads to identify barriers and facilitators to effective PPI.
Results: Eight PREFER case studies involved patients as research partners. Patient partners were involved in activities spanning all phases of the patient preference research process, including in study design, conduct and dissemination. However, the type and degree of patient partner involvement varied considerably. Positive impacts of PPI included improvements in the: (1) quality of the research and research process; (2) patient partner empowerment; (3) study transparency and dissemination of results; (4) research ethics, and (5) trust and respect between the research team and the patient community. Of the 13 barriers identified, the 3 most frequently reported were inadequate resources, insufficient time to fully involve patient partners, and uncertainty regarding how to operationalize the role of 'patient partner. Among the 12 facilitators identified, the two most frequently cited were (1) having a clearly stated purpose for involving patients as research partners; and (2) having multiple patient partners involved in the study.
Conclusion: PPI had many positive impacts on the PREFER studies. Preference study leads with prior PPI experience reported a greater number of positive impacts than those with no such experience. In light of the numerous barriers identified, multi-faceted implementation strategies should be considered to support adoption, integration and sustainment of PPI within preference research. Additional case studies of patient partner involvement in preference research are needed as well to inform best practices in this area.
Keywords: Medical product decision-making; Patient and public involvement/engagement (PPI); Patient impact; Patient involvement; Patient preference study; Patient preferences; Patient research partners.
Plain language summary
Research about patients’ preferences for medicinal products and treatments is growing. Such research could be improved if patients were involved as ‘research partners,’ that is, as active members of the study team itself. To date, however, little is known about the actual experience of involving patients as partners in such research. This paper presents learnings from involving patients as partners in 8 case studies conducted as part of IMI-PREFER, a big, European-based project which aimed to develop recommendations about how to conduct preference research. Involving patients as partners led to improvements in the: (1) quality of the research and research process; (2) recruitment of participants; (3) content and design of patient-facing informational materials; and, (4) how and what study results were shared with patient communities. Our findings showed that it is important to plan for patient partners’ involvement early on in the design of the preference study so as to ensure that they are fully integrated into the research team and their opportunity to contribute to all stages of the research is optimized. Such planning should address how patient partners will be paid, what their role responsibilities will include, how and when they will be trained and educated, and how they will be supported throughout the course of the study. Having a clearly stated purpose for involving patients as research partners, selecting patient partners who have had prior research experience and relationships with the researchers, and having multiple patient partners on the study team are all also helpful in supporting successful patient involvement. We need more people to share their experiences with involving patient partners in preference research so that we can continue to improve how this is done.
© 2023. The Author(s).
Conflict of interest statement
MYS was a fulltime employee of AstraZeneca plc and a shareholder in the company at the time that this study was conducted. MYS is currently a fulltime employee of Evidera, Inc., PPD, a part of Thermo Fisher Scientific. MM is a fulltime employee of Novartis and a shareholder in the company. All other co-authors (IC, MF, IH, RJ, SO, GS, and VS) have no conflicts of interest to report. This article and its contents reflect the authors’ personal views and not the view of PREFER, IMI, the European Union or EFPIA, or any organization with which any of the authors are affiliated.
Similar articles
-
Developing catalyst films of health experiences: an analysis of a robust multi-stakeholder involvement journey.Res Involv Engagem. 2022 Jul 29;8(1):34. doi: 10.1186/s40900-022-00369-3. Res Involv Engagem. 2022. PMID: 35906697 Free PMC article.
-
The value of involving patients and public in health services research and evaluation: a qualitative study.Res Involv Engagem. 2021 Jun 29;7(1):49. doi: 10.1186/s40900-021-00289-8. Res Involv Engagem. 2021. PMID: 34187590 Free PMC article.
-
A qualitative systematic review of internal and external influences on shared decision-making in all health care settings.JBI Libr Syst Rev. 2012;10(58):4633-4646. doi: 10.11124/jbisrir-2012-432. JBI Libr Syst Rev. 2012. PMID: 27820528
-
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.
-
Patient and Public Involvement in Technology-Related Dementia Research: Scoping Review.JMIR Aging. 2024 Mar 4;7:e48292. doi: 10.2196/48292. JMIR Aging. 2024. PMID: 38437014 Free PMC article.
Cited by
-
Patient and public involvement in the development of the digital tool MyBoT to support communication between young people with a chronic condition and care providers.Health Expect. 2024 Apr;27(2):e14003. doi: 10.1111/hex.14003. Health Expect. 2024. PMID: 38444291 Free PMC article.
-
EULAR recommendations for the involvement of patient research partners in rheumatology research: 2023 update.Ann Rheum Dis. 2024 Oct 21;83(11):1443-1453. doi: 10.1136/ard-2024-225566. Ann Rheum Dis. 2024. PMID: 38876509 Free PMC article.
-
The impact of a patient advisory board on a clinical comparative effectiveness trial: a comparison of patient and researcher perspectives.J Comp Eff Res. 2025 Mar;14(3):e240050. doi: 10.57264/cer-2024-0050. Epub 2025 Jan 30. J Comp Eff Res. 2025. PMID: 39881634 Free PMC article. Clinical Trial.
-
The HEALERS: a patient, community, and stakeholder advisory board focus group series to refine a novel virtual world-based cardiac rehabilitation intervention and clinical trial.Front Digit Health. 2025 Jul 15;7:1427539. doi: 10.3389/fdgth.2025.1427539. eCollection 2025. Front Digit Health. 2025. PMID: 40735343 Free PMC article.
-
Frameworks Used to Engage Postsecondary Students in Campus Mental Health Research: A Scoping Review.Health Expect. 2025 Apr;28(2):e70144. doi: 10.1111/hex.70144. Health Expect. 2025. PMID: 40116286 Free PMC article.
References
-
- European Medicines Agency (EMA). Regulatory science to 2025 strategy. 2020. https://www.ema.europa.eu/en/documents/regulatory-procedural-guideline/e....
-
- European Commission (EC). Pharmaceutical strategy for Europe 2020. 2020. https://health.ec.europa.eu/system/files/2021-02/pharma-strategy_report_....
-
- US Food and Drug Administration Guidance to Industry. Patient preference information – voluntary submission, review in premarket approval applications, humanitarian device exemption applications, and de novo requests, and inclusion in decision summaries and device labeling: guidance for industry, Food and Drug Administration staff, and other stakeholders. U.S. Department of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health and Center for Biologics Evaluation and Research 2016. https://www.fda.gov/media/92593/download.
-
- International Council on Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use. ICH harmonised guideline. Revision of M4E guideline on enhancing the format and structure of benefit-risk information in ICH Efficacy-M4E(R2). https://database.ich.org/sites/default/files/M4E_R2__Guideline.pdf.