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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05895279
Other study ID # 21-006715
Secondary ID NCI-2022-0990621
Status Completed
Phase N/A
First received
Last updated
Start date August 2, 2021
Est. completion date September 30, 2021

Study information

Verified date May 2024
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This phase III trial determines how well the Minority Prostate Cancer (MiCaP) Research Digest works in providing information to black men about the latest prostate cancer research. MiCaP Research Digest may be an effective method to help people learn about prostate cancer.This goal of this trial is to create educational programming that helps Black men make informed decisions about their prostate healthcare since Black men are diagnosed with prostate cancer more than any other race or ethnicity.


Description:

PRIMARY OBJECTIVE: I. To develop a research dissemination program, the Minority Prostate Cancer (MiCaP) Research Digest, which will spread information about CaP scientific discoveries, evidence-based interventions, and open clinical trials instantly among black males (BM). OUTLINE: Participants are randomized to 1 of 2 arms. ARM I: Participants watch MiCaP Research Digest video on study. Participants complete a survey throughout the trial. ARM II: Participants watch an alternative video on study. Participants complete a survey throughout the trial.


Recruitment information / eligibility

Status Completed
Enrollment 220
Est. completion date September 30, 2021
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender Male
Age group 35 Years to 70 Years
Eligibility Inclusion Criteria: - Identify as a Black male - Between the ages of 35 and 70 - For virtual data collection, have access to the internet and Zoom (if joining study online) - For virtual data collection, reside anywhere in the U.S. - For in-person data collection, reside in one of the nine (9) catchment areas of the Mayo Clinic Cancer Center: Baker, Duval, Nassau, Clay, St. John's, Putnam, Flagler, Volusia and Brevard Exclusion Criteria: - Identify as a race or ethnicity that is not Black - Identify as female - Be younger than age 35 and older than age 70 - Lack access to internet and Zoom (if joining study online)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Media Intervention
Watch MiCaP Research Digest video
Media Intervention
Watch alternate video
Survey Administration
Complete survey

Locations

Country Name City State
United States Mayo Clinic in Florida Jacksonville Florida

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in perception of access to medical services and general health Using the Minority Prostate Cancer (MiCaP) survey developed for this study, participants are asked 10 questions regarding access to medical services and general health with a yes/no response. Baseline, 1 hour after video intervention
Primary Change in perception in participation with clinical trials about prostate cancer Using the Minority Prostate Cancer (MiCaP) survey developed for this study, participants are asked 10 questions regarding views on participating in clinical trials about prostate cancer with a yes/no response. Baseline, 1 hour after video intervention
Primary Change in perception of familiarity with prostate cancer research Using the Minority Prostate Cancer (MiCaP) survey developed for this study, participants are asked 5 questions regarding views on participating in clinical trials about prostate cancer with a true/false/don't know response. Baseline, 1 hour after video intervention
Primary Change in perception of familiarity with a research study protocol Using the Minority Prostate Cancer (MiCaP) survey developed for this study, participants are asked 5 questions regarding information about a study protocol with a true/false/don't know response. Baseline, 1 hour after video intervention
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