The Cerebral Palsy Research Network, United Cerebral Palsy and CanChild are excited to present and discuss what it means for community members – people with lived experience and their caregivers – to engage in the research process. Engaging in the research process is not about being a study participant though that is a great way to support CP research too. Instead, it is about how YOU can influence the research that gets conducted – what study questions are important, how should they be defined, what are the outcomes that are important to participants and how should the results be shared with the medical and cerebral palsy (CP) communities.
Click here to see Community Engagement in Research
