I n recent years, there has been increasing interest in conducting randomized controlled trials (RCTs) that are pragmatic in orientation. 1,2 Pragmatic trials use study settings and methods similar to usual care, as well as taking into account the perspectives of patients. 3,4 Some of the design features of pragmatic trial design -for example, selecting outcomes that are important to patients 5 -overlap with objectives of patient-oriented research. [6][7][8] Patient and public involvement (PPI) in research provides an opportunity for patients and families to share their lived experiences and better align research with patient values and priorities. 6 For the purpose of this research and in alignment with the Canadian Institutes of Health Research (CIHR) Strategy for Patient-Oriented Research (SPOR), 6 we define PPI as "researchers consulting or working with members of the public, patients, service users, and carers in any or all part(s) of the research process, including the choice of research topic, design, planning, conduct or dissemination of research." 9 We refer to these individuals as "PPI partners"; partners could include, for example, grant co-applicants, members of a Trial Steering Committee, or members of a patient or public advisory panel. In health research, PPI is strongly encouraged by international funding bodies, 6,10,11 institutions 12 and stakeholder groups. 13,14 Previous reviews of RCTs found low prevalence of PPI, with inconsistent reporting. [15][16][17][18][19][20][21] However, no trial-specific reporting guidelines require authors to indicate whether their trial included PPI (although the generic Guidance for Reporting Involvement of Patients and the Public [GRIPP2] 22 checklist may be used when PPI was part of an intervention), and journals rarely require PPI to be reported. 17 Relying