- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05980182
Engaging Black Men in Colorectal Cancer Screening (SUCCEED)
August 4, 2025 updated by: Virginia Commonwealth University
SUCCEED: Engaging Black Men in Colorectal Cancer Screening (CRC) Screening
To determine the unmet needs, attitudes, barriers and facilitators of African American (AA)/ Black men use of colorectal cancer screening and describe how community leaders such as barbers may act as Community Champions to educate and facilitate screening participation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Virginia
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Richmond, Virginia, United States, 23298
- Virginia Commonwealth University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Adult men
- Identify as Black or African American
- Work or live in Petersburg, VA or surrounding counties
- Eligible for colorectal cancer (CRC) screening at time of study enrollment
Exclusion Criteria:
- Inability to speak or read English
- Currently up-to-date with CRC screening
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Tailored Screen to Save (S2S) content
Content to be delivered using a combination of short video and text-based information optimized for delivery via Quick Response (QR) codes for smartphones.
|
Self-directed application (app) that is downloaded to the participant's personal device.
The app contains five informational videos, that provide an orientation to the content on the app, and discuss what colorectal cancer is, and the type of CRC screening tests that are available as well as a video with a personal history.
There is a a National Cancer Institute (NCI) risk calculation tool, and a family history infographic.
Once the videos have been viewed participants have the option to indicate if they wish to receive a call from the healthcare clinic to discuss scheduling an appointment for screening.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Colorectal Screening Status
Time Frame: 3 Months
|
The number of participants that complete screening (any type)
|
3 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Determine Feasibility of Mobile Health (mHealth) Application -Enrollment
Time Frame: Week 1
|
The number of men that enroll for the intervention (application)
|
Week 1
|
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Determine the Feasibility of the mHealth Application-Videos
Time Frame: Week 1
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The number of participants that view the videos
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Week 1
|
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Determine the Feasibility of the mHealth Application- Retention
Time Frame: Baseline (Day 1), Week 2, and Week 12
|
The number of participants that complete Questionnaires (>65%)
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Baseline (Day 1), Week 2, and Week 12
|
|
Determine the Feasibility of the mHealth Application- Clinic/ Screening Request
Time Frame: Week 12
|
The number of participants that respond to the request to contact clinic/ navigation services
|
Week 12
|
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Determine the Feasibility of the mHealth Application - Sharing Content
Time Frame: Week 12
|
The number of participants that share content on social network
|
Week 12
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Maria Thomson, Ph.D., Virginia Commonwealt University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 5, 2023
Primary Completion (Actual)
June 25, 2024
Study Completion (Actual)
June 25, 2024
Study Registration Dates
First Submitted
July 27, 2023
First Submitted That Met QC Criteria
August 4, 2023
First Posted (Actual)
August 7, 2023
Study Record Updates
Last Update Posted (Actual)
August 20, 2025
Last Update Submitted That Met QC Criteria
August 4, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MCC-21-18632
- HM20023619 (Other Identifier: Virginia Commonwealth University)
- CA264067-01 (Other Grant/Funding Number: NCI)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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