- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01072851
Tools for Improving Colorectal Cancer Screening Rates: Multimedia Versus Print
Tools for Improving Colorectal Cancer Screening Rates: Multimedia vs Print
The objective of this study is to compare the effectiveness of multimedia and print tools designed to provide patients at safety-net clinics with comprehensible information about colorectal cancer screening and motivate them to complete screening.The print and multimedia interventions were constructed with parallel content to allow valid comparison of format-related effects on knowledge and screening rates.These easy to use tools will provide under served patients at community health centers with clear and consistent messages about colorectal Cancer(CRC) and CRC screening, delivered immediately before the patients see a doctor.
Specific Aims
- To determine if multimedia and print interventions that provide patients with information and motivational messages about CRC screening increase screening rates above usual care.
Determine whether showing patients a multimedia program achieves higher CRC screening rates than does a print booklet with equivalent messages.
- Examine if the effects of these multimedia and print interventions on CRC screening rates differ with literacy level.
- Examine if the effects of these multimedia and print interventions on CRC screening differ with race/ethnicity
- Examine if these multimedia and print interventions have differential effects on knowledge relevant to CRC screening.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Despite the clear benefits of screening for early detection and prevention of colorectal cancer, as many as half of eligible adults remain unscreened. Poor and under served populations, particularly African American and Latino/Hispanic adults, are at greatest risk for noncompliance with recommended tests. Health education strategies developed to date have led to relatively minimal gains, resulting in little translation to routine clinical practice. This is especially true in more difficult, resource-strained practice settings, such as community health centers.
The interventions in the proposed study draw on communication science to optimize message design, use communication technology to optimize message delivery and include parallel content in both print and multimedia versions to allow comparison of format-related effects on both knowledge and screening rates.The multimedia and print tools are based on patient education programs that we developed with extensive attention to theory as well as community member input.
Study Type
Enrollment (Actual)
Phase
- Phase 3
Contacts and Locations
Study Locations
-
-
Illinois
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Highland Park, Illinois, United States, 60085
- Midlakes Medical Building
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North Chicago, Illinois, United States, 60064
- North Chicago Health Center
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Waukegan, Illinois, United States, 60085
- Belvidere Medical Building
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 50-80 years of age,
- Registered for an appointment at one of the target clinics,
- Speaks English or Spanish.
Exclusion Criteria:
- Patient has had CRC screening in the past 12 months,
- Unable to review the study materials because of language, physical condition or literacy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Multimedia educational tool
Multimedia education tool - A culturally competent video explaining the importance of and the process of colorectal cancer screening
|
A four minute exposure to an educational video with controlled content on the importance of colorectal cancer screening and explaining the processes and procedures.
Other Names:
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Experimental: Print educational tool
Print media - A culturally competent printed brochure explaining the importance of and the process of colorectal cancer screening
|
Exposure to a printed brochure with controlled content on the importance of colorectal cancer screening and explaining the processes and procedures.
Other Names:
|
Active Comparator: No intervention
Usual and customary waiting room process - Usual and customary office waiting period with access to standard nationally generated colorectal cancer screening informational material in the waiting room and/or exam room.
|
No specialized educational intervention to promote colorectal cancer screening or to explain the process
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Comparison of the acceptance of colorectal cancer screening by patients who view print or multimedia educational tools
Time Frame: 3 months post visit
|
3 months post visit
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Role of race/ethnicity and literacy levels on the comparative effects if the intervention
Time Frame: At scheduled appointment
|
At scheduled appointment
|
Comparative knowledge of colorectal cancer screening by patients who view the print or multi-media educational tools.
Time Frame: At the scheduled patient visit
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At the scheduled patient visit
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Gregory Makoul, PHD, St. Francis Hospital and Medical Center
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0910001-E
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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