There is a growing body of evidence in support of more active engagement of patients in health research, beyond the traditional role of a subject or participant, which has led to the realization that their perspectives are a critical component of effective health research.1,2 This importance has recently been acknowledged in a number of countries, including the United Kingdom, the United States, and Canada. For example, the Canadian Institutes of Health Research has established the Strategy for Patient-Oriented Research, a coalition of federal, provincial, and territorial partners all dedicated to supporting researchers in integrating patients into all phases of research to better inform practice for improved patient outcomes. The partners include a mix of stakeholders, such as patients (ie, parents, caregivers, family, and public members), researchers, health professionals, and policy makers, among others. Patient-oriented research is defined in the Strategy for Patient-Oriented Research initiative as a continuum...

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