Colon Cancer Clinical Trial

Interactive Computer Program or Brochure in Increasing Colorectal Cancer Screening Among African Americans

Summary

RATIONALE: An interactive computer program may be more effective than a brochure in increasing colorectal cancer screening among African Americans.

PURPOSE: This randomized clinical trial is studying an interactive computer program to see how well it works compared with a brochure in increasing colorectal cancer screening among African Americans.

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Full Description

OBJECTIVES:

Compare rates of participation in fecal occult blood testing and endoscopic screening (colonoscopy or sigmoidoscopy) among African-Americans who receive an interactive computer intervention (ICI) versus a non-tailored colorectal cancer screening brochure.
Examine mediators and moderators of intervention effectiveness as depicted in the conceptual model.

OUTLINE: This is a multicenter study.

Participants are stratified according to site, age (≤ 65 years old vs > 65 years old) and gender. Participants are randomized to one of two arms.

Arm I (non-tailored colorectal cancer screening brochure): Participants undergo a baseline interview via telephone and receive a colorectal cancer screening brochure in the clinic prior to visit with healthcare provider. Participants then undergo telephone interviews at 1 week, 6 months, and 15 months.
Arm II (interactive computer intervention [ICI]): Participants undergo a baseline interview via telephone and complete an ICI in the clinic prior to visit with healthcare provider. Participants then undergo telephone interviews at 1 week, 6 months, and 15 months.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Currently being seen in the primary care clinics of Wishard Memorial Hospital (Indianapolis, IN), Roudebush Veterans Affairs Medical Center (Indianapolis, IN), IU Health Family Medicine Center (Indianapolis, IN) or Norton Louisville Primary Care Clinic (Louisville, KY)

African-American who is currently non-adherent to screening guidelines, meeting all of the following criteria:

No fecal occult blood test in the past 12 months
No sigmoidoscopy in the past 5 years
No colonoscopy in the past 10 years
Patients with average and increased risk for colorectal cancer are eligible
No personal history of colorectal cancer

PATIENT CHARACTERISTICS:

Participants must have a telephone
English-speaking
Able to read at a 5th grade reading level
No medical condition that prohibits colorectal cancer screening

PRIOR CONCURRENT THERAPY:

See Disease Characteristics

Study is for people with:

Colon Cancer

Estimated Enrollment:

693

Study ID:

NCT00672828

Recruitment Status:

Completed

Sponsor:

Indiana University

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There is 1 Location for this study

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Indiana University School of Nursing
Indianapolis Indiana, 46202, United States

How clear is this clinincal trial information?

Study is for people with:

Colon Cancer

Estimated Enrollment:

693

Study ID:

NCT00672828

Recruitment Status:

Completed

Sponsor:


Indiana University

How clear is this clinincal trial information?

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