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Table 3 Adapted Guidance for Reporting Involvement of Patients and the Public 2, short form [15]

From: Patient and public involvement in dementia research in the European Union: a scoping review

Section and topic Item
1: Countrya EU country the PPI study was conducted
2: Aim Report the aim of PPI
3: PPI term useda Term used to describe PPI
4: Populationa Which patient or public population took part in PPI
5: Methods Provide a clear description of the methods used for PPI
6: Study results Report the results of PPI on the research process impact on researchers and PPI members, including both positive and negative outcomes
7: Discussion and conclusions Comment on the extent to which PPI influenced the study overall
8: Reflections/critical perspective Comment critically on the study, reflecting on the aspects of involvement that went well and those that did not
9: Evaluation methodsa Methods used to evaluate the impact of PPI on researchers, on patient and public involved, on the research process
10: Findings from evaluationa The impact of PPI on researchers, on patient and public involved, on the research process
  1. (aadapted sections)