We will collaborate with members of Black communities, NHS providers and wider stakeholders across the UK to conduct the research in four phases.
Phase 1
Interviews, focus groups and surveys with Black men diagnosed with prostate cancer, Black men without prostate cancer and immediate families of Black men with prostate cancer to understand their experiences/perceptions of stigma. By Families, we mean those who may influence men’s decision-making, such as partners.
Phase 2
Stakeholder engagement workshops with Black men and their families to discuss findings from phase one and develop resources which are culturally appropriate with them (such as videos, pocket guides) to inform public health messaging on prostate cancer.
Phase 3
Focus groups with Black men and their families to test if the resources developed are acceptable to them. We will use their comments and feedback to improve the resources so they are useful in clinical and community settings.
Phase 4
Test how practical it will be to integrate the resources within clinical and community settings to improve patient care and early engagement with cancer services among Black men in the UK.