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Educational Intervention for Colorectal Cancer Screening
N/A
Waitlist Available
Led By Electra Paskett, PhD
Research Sponsored by Ohio State University Comprehensive Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Participants from Franklin County or from Appalachia Ohio (depending on program location
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to two years
Awards & highlights
No Placebo-Only Group
Summary
This trial looks at how well educational tools help improve people's knowledge of colorectal cancer and rates of cancer screening.
Who is the study for?
This trial is for individuals from Franklin County or Appalachia Ohio. It's designed to see if certain educational tools can increase understanding and screening rates for colorectal cancer.
What is being tested?
The study tests the effectiveness of an educational intervention, which includes using an inflatable colon model, PowerPoint presentations, or flip books/charts to boost knowledge and screenings for colorectal cancer.
What are the potential side effects?
Since this is an educational intervention rather than a medical treatment, there are no direct physical side effects expected from participating in this trial.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to two years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to two years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in knowledge and degree to which reported intentions regarding colorectal cancer screening are related to the educational session
Change in knowledge and strength of intention to be screened
Frequency of reported family history of colorectal cancer
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Screening (educational intervention)Experimental Treatment2 Interventions
Participants attend educational sessions comprising of an inflatable colon interactive exhibit that allows visitors to walk through a colon while seeing images, a PowerPoint presentation that contains messages that are tailored to meet the cultural and linguistic needs of Black/African Americans, Appalachians, and Hispanics/Latinos, and or flip books/flip charts. Participants also receive a copy of the study information sheet which contains the basic elements of informed consent and a pre-education session knowledge survey.
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Who is running the clinical trial?
Ohio State University Comprehensive Cancer CenterLead Sponsor
340 Previous Clinical Trials
294,295 Total Patients Enrolled
National Cancer Institute (NCI)NIH
13,925 Previous Clinical Trials
41,017,800 Total Patients Enrolled
Electra Paskett, PhDPrincipal InvestigatorOhio State University Comprehensive Cancer Center
3 Previous Clinical Trials
1,341 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Screening (educational intervention)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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