Status:

COMPLETED

Computer-Based Tailored or Standard Information for Colorectal Cancer Screening

Lead Sponsor:

University of Michigan Rogel Cancer Center

Collaborating Sponsors:

National Cancer Institute (NCI)

Conditions:

Colorectal Cancer

Eligibility:

All Genders

50-79 years

Brief Summary

RATIONALE: A computer program that provides information on colorectal cancer screening based on a patient's test preferences may be more effective than a computer program that gives standard informati...

Detailed Description

OBJECTIVES: * To evaluate the effectiveness of a preference-tailored (PT) intervention vs standard information (SI) delivered via computer for increasing patients' adherence to colorectal cancer (CRC...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • At average risk for colorectal cancer (CRC), defined as the following:
  • No personal history of CRC, adenomatous colon polyps, or inflammatory bowel disease
  • No family history of CRC
  • Not up-to-date with CRC screening in past year OR have never been screened, defined as
  • Up-to-date screening is defined as having completed 1 of the following:
  • Fecal occult blood test within the past 2 years
  • Sigmoidoscopy within the past 5 years
  • Colonoscopy with the past 10 years
  • Double-contrast barium enema within the past 5 years
  • Patient at San Francisco Community Health Network or at Henry Ford Health System and a member of the Health Alliance Plan
  • PATIENT CHARACTERISTICS:
  • Life expectancy ≥ 1 year
  • No history of inflammatory bowel disease, polyposis, or hereditary nonpolyposis
  • No severe comorbidity or significantly lowered life expectancy, including any of the following:
  • Do not resuscitate (DNR)/do not intubate (DNI) code status
  • Metastatic cancer
  • End-stage congestive heart failure
  • Severe chronic obstructive pulmonary disease
  • Coronary artery disease with recent myocardial infarction or unstable angina
  • Dementia
  • PRIOR CONCURRENT THERAPY:
  • No prior bowel resection

Exclusion

    Key Trial Info

    Start Date :

    August 1 2004

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    May 1 2008

    Estimated Enrollment :

    345 Patients enrolled

    Trial Details

    Trial ID

    NCT00955188

    Start Date

    August 1 2004

    End Date

    May 1 2008

    Last Update

    December 21 2012

    Active Locations (3)

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    Page 1 of 1 (3 locations)

    1

    UCSF Helen Diller Family Comprehensive Cancer Center

    San Francisco, California, United States, 94115

    2

    University of Michigan Comprehensive Cancer Center

    Ann Arbor, Michigan, United States, 48109-0942

    3

    Josephine Ford Cancer Center at Henry Ford Hospital

    Detroit, Michigan, United States, 48202