- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04812743
Colorectal Health Research Champions
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Virginia
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Richmond, Virginia, United States, 23298
- Virginia Commonwealth University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
the individual is > 30 years of age
- They are literate
- They are/were directly or indirectly impacted by colorectal cancer and interested in becoming a champion for colorectal cancer research.
To participate in a chat hosted by the CHRC the inclusion criteria is:
- adult of any gender
- over 30 years of age.
Exclusion Criteria for chat hosted by the CHRC:
-Those < 30 years of age
Study Plan
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: Colorectal Health Research Champion trainees
Colorectal Health Research Champion (CHRC) trainees receive 5 education sessions on colorectal cancer, clinical research, biospecimen donation, ethics, and presentation skills.
The CHRCs will invite others in their social networks to present to them this educational information, following the train the trainer model of health education.
|
20 Colorectal Health Research Champions will be recruited from the VCU Massey Cancer Center Catchment Area (66 counties in Virginia) The Colorectal Health Research Champions will receive training in four specific areas during group educational sessions. Colorectal Health Research Champions will be asked to disseminate the four defined messages on at least two occasions to small groups in their social network in a venue of their choice (house chats, faith-based, social gatherings, family gatherings, etc.). We ask that each CHRC participant host 2 chats with 5-10 people in attendance at each chat. We expect that at least 200 participants will be invited to chats through 10 CHRCs. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Increase in participants knowledge and intentions related to colorectal cancer screening.
Time Frame: 4 months
|
Participant knowledge will be measured using pre/post questionnaires, with each correct answer being worth one point (14 total points) Higher summary scores indicate a greater change in knowledge.
Intentions are measured on a 5 -point likert scale.
|
4 months
|
|
Increase in knowledge and intentions related to biospecimen donation and clinical trial participation.
Time Frame: 4 months
|
Participant knowledge and intentions related to biospecimen donation and clinical trial participation will be measured using pre/post questionnaires, with each correct answer being worth one point (20 total points).
Higher summary scores indicate a greater change in knowledge.
Intentions are measured on a 5 -point likert scale.
|
4 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Vanessa B Sheppard, PhD, Virginia Commonwealth University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MCC-19-15899
- HM20017398 (Other Identifier: Virginia Commonwealth University IRB)
- NCI-2019-08595 (Other Identifier: NCI)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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