Sponsor study identifier
Secondary identifiers
OTHER · National Cancer Institute
interventional
24
1 country
1
Study Start
February 6, 2025
Actual (reported)Primary Completion
October 29, 2025
Actual (reported)Study Completion
October 29, 2025
Actual (reported)To learn about barriers to prostate cancer screening in Black, faith-based communities. Investigators will use the information collected in this study to create a prostate cancer education program that is relevant to Black men within the church and improve prostate cancer screening.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
October 29, 2025
Actual (reported)Click on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
February 6, 2025
Actual (reported)February 6, 2025
Actual (reported)February 20, 2025
Actual (reported)October 29, 2025
Actual (reported)October 29, 2025
Actual (reported)Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
Through study completion, an average of 1 year.
Participants will be asked about your views and personal opinions on barriers of prostate cancer screening in the Black community, with a specific focus on Black men in church. Participants will also watch an educational video about prostate cancer and review specialized prostate cancer guidelines for Black men and will be asked to provide feedback about these materials. The focus group will take about 2 hours to complete and will be led by the study Investigator and a research coordinator. A member of the research team will also take notes during the focus group, and the discussion will also be audio recorded and transcribed (written down word for word). Additionally, participant demographic information will be collected (such as your age).
The focus group will take about 2 hours to complete and will be led by the study Investigator and a research coordinator. A member of the research team will also take notes during the focus group, and the discussion will also be audio recorded and transcribed (written down word for word). Additionally, participant demographic information will be collected (such as your age).
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
MD Anderson Cancer Center
Houston, Texas, 77030, United States
Matthew T Smith
M.D. Anderson Cancer Center
24 participants (actual enrollment reported by the registry).
First Submitted
February 6, 2025
First Posted
February 20, 2025
Study Start
February 6, 2025
Actual (reported)Contact the study team to confirm eligibility.
Primary Completion
October 29, 2025
Actual (reported)Study Completion
October 29, 2025
Actual (reported)Last Updated
October 31, 2025
Record last verified: 2025-10
Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.
Source: ClinicalTrials.gov.
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