Diversity on a mental health research register: Barriers and Facilitators to the Consent for Contact Register | C4C
This study aims to help guide investigators initiating or conducting research participation registries to understand the potential barriers to enrolling participants and the preferences that these individuals have related to registry models and operations. The primary objective of this study is to explore the reasons why service user groups who are underrepresented on C4C say no to joining the C4C research register.