Meaningful and active collaboration between researchers and persons with lived experience of arthritis (patients, caregivers, family members and friends) improves the relevance and impact of research. As a result, many funding agencies now require persons with lived experience to be actively involved in the governance, priority setting, conduct and translation of research. This shift has generated widespread enthusiasm for involving patients as partners in health research. However, patient engagement in research goes beyond buzzwords, and there is no one-size fits-all approach.
This webinar will discuss different forms of patient engagement, focusing on the importance of matching researchers’ needs and patient knowledge, navigating power dynamics, providing training and support for patient and research, and fostering regular reflection within research teams to enhance their engagement practices