Abstract
Background:
Patient and public involvement in research (PPI) aims to increase the quality and relevance of research by incorporating the perspective from those ultimately affected by the research. Despite these potential benefits, PPI is rarely included in epidemiology protocols.
Objective:
to provide an overview of methods used for PPI and offer practical recommendations for the efficient implementation in epidemiological research.
Methods:
We conducted a review on PPI methods. We mirrored it with a patient advocate’s viewpoint about PPI. We then identified key steps to optimize PPI in epidemiological research based on our review and the viewpoint of the patient advocate taking into account the identification of barriers and facilitation of PPI. From these, we provided practical recommendations to launch a patient-centered cohort study. We used the implementation of a new digital cohort study as an exemplary use case.
Results:
We analyzed data from 98 studies, with 59% of studies performed in the United Kingdom. The most common methods were workshops (48.5%), meetings, events or conferences (35.1%), surveys (34.0%), focus groups (26.0%), interviews (23.7%), consensus techniques (8.2%), experience-based co-design (8.2%), James Lind Alliance (7.2%), and social media analysis (6.2%). The viewpoint of a patient showed a strong interest in participating in research. Research ideas (61.2%), co-design (42.9%), defining priorities (30.6%), participation in data analysis (26.5%) and being member of the steering committee (16.5%) were the most usual PPI modalities. We identified 8 general recommendations and 32 key PPI-related steps that can serve as guidelines to increase the relevance of epidemiological studies.
Conclusions:
PPI is a project within a project that contributes to improving knowledge and increasing the relevance of research. PPI methods are mainly used for ideas generation. Based on our review and case study, we recommend to include PPI at an early stage and through all the research cycles and to combine methods for generation of new ideas. For e-cohorts, the use of digital tools are essential to scale up PPI. We encourage investigators to rely on our practical recommendations to extend PPI in future epidemiological studies.
Patient and public involvement in research (PPI) aims to increase the quality and relevance of research by incorporating the perspective from those ultimately affected by the research. Despite these potential benefits, PPI is rarely included in epidemiology protocols.
Objective:
to provide an overview of methods used for PPI and offer practical recommendations for the efficient implementation in epidemiological research.
Methods:
We conducted a review on PPI methods. We mirrored it with a patient advocate’s viewpoint about PPI. We then identified key steps to optimize PPI in epidemiological research based on our review and the viewpoint of the patient advocate taking into account the identification of barriers and facilitation of PPI. From these, we provided practical recommendations to launch a patient-centered cohort study. We used the implementation of a new digital cohort study as an exemplary use case.
Results:
We analyzed data from 98 studies, with 59% of studies performed in the United Kingdom. The most common methods were workshops (48.5%), meetings, events or conferences (35.1%), surveys (34.0%), focus groups (26.0%), interviews (23.7%), consensus techniques (8.2%), experience-based co-design (8.2%), James Lind Alliance (7.2%), and social media analysis (6.2%). The viewpoint of a patient showed a strong interest in participating in research. Research ideas (61.2%), co-design (42.9%), defining priorities (30.6%), participation in data analysis (26.5%) and being member of the steering committee (16.5%) were the most usual PPI modalities. We identified 8 general recommendations and 32 key PPI-related steps that can serve as guidelines to increase the relevance of epidemiological studies.
Conclusions:
PPI is a project within a project that contributes to improving knowledge and increasing the relevance of research. PPI methods are mainly used for ideas generation. Based on our review and case study, we recommend to include PPI at an early stage and through all the research cycles and to combine methods for generation of new ideas. For e-cohorts, the use of digital tools are essential to scale up PPI. We encourage investigators to rely on our practical recommendations to extend PPI in future epidemiological studies.
Original language | English |
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Article number | e25743 |
Journal | Journal of Medical Internet Research |
Volume | 23 |
Issue number | 12 |
DOIs | |
Publication status | Published - 23 Dec 2021 |
Keywords
- patient and public involvement
- workshops
- surveys
- co-design
- mobile phone
- digital cohort study
- digital epidemiology
- social media