A Lived Experience-led rapid scoping review of 81 peer-reviewed and grey literature publications confirmed that the people most impacted by mental health research — consumers, families, carers, supporters and kin — are routinely excluded from defining research questions, contributing to data collection and analysis, and learning the outcomes of research they participated in.
Despite more than 20 years of calls in policy and peer-reviewed literature for meaningful Lived Experience inclusion, mainstream research practices have changed little. People with Lived Experience are frequently left out of technical research activities and confined to the role of participant rather than active contributor or leader. The report argues that capability building, mentoring, and intentional opportunity creation are essential to change this.