Diversity on a mental health research register: Barriers and Facilitators to the Consent for Contact Register. | C4C
To investigate the reasons why underrepresented service users, say no to registering to consent for contact. These findings aim to make an important contribution to the continuous advancement of the C4C model, minimising the negative reactions from patients (Cunningham, 2017) and allowing them to participate in research through an informed decision (Oduola et al., 2017).