About this trial
The goal of this randomised feasibility trial is to examine feasibility and acceptability of a co-produced and faith-placed intervention to increase uptake of breast, cervical, bowel, and abdominal aortic aneurysm (AAA) screening among Black communities in the North East of England, Leeds and Scotland, United Kingdom (UK).
Participants will be invited to attend a two-hour workshop at each of the three study sites and will be randomly assigned to either the intervention group or the control group.
This 24-month feasibility study will inform the development of a full-scale randomised-controlled trial co-produced for Black people that uses culturally appropriate messages that support screening for early diagnosis in this underserved group.
Eligibility criteria
Qualifiers
Members of participating churches (North East of England, Leeds, Scotland)
Self-identify as Black,
Female aged 25-74,
Male aged 50-74,
Disqualifiers
Not a member of participating churches (North East of England, Leeds, Scotland).
Individuals who do not self-identify as Black
Do not self-identity as Black
Females aged outside the range of 25-74
Trial design
Treatments tested in this trial
- Faith-placed intervention to promote breast, cervical, bowel, and AAA screening uptake in Black communities.
Treatment groups
Sponsors and collaborators
University of Sunderland
Lead sponsor
University of Glasgow
Collaborator