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Clinical Trials/NCT03100461
NCT03100461
Completed
Not Applicable

Adaptive Intervention to Maximize Colorectal Screening in Safety Net Populations

University of Kansas Medical Center1 site in 1 country500 target enrollmentJanuary 22, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Cancer
Sponsor
University of Kansas Medical Center
Enrollment
500
Locations
1
Primary Endpoint
CRC screening completion rate
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this study is to find the best ways to increase colorectal cancer (CRC) screening.

Detailed Description

Colorectal Cancer is preventable and curable but is still the second most common cause of cancer death in the U.S. Minorities and those with low income have more CRC than middle and high income Whites.. They also get fewer CRC screening tests. Low knowledge of CRC screening may, in part, drive this lower test use. We need new ways to improve CRC screening in primary care clinics where many minority and uninsured patients receive health care.

Registry
clinicaltrials.gov
Start Date
January 22, 2018
End Date
September 30, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Have a home address and access to a working telephone
  • Pass Mini-Cog assessment

Exclusion Criteria

  • FIT (fecal immunochemical test) test within 1 year, Sigmoidoscopy or Barium enema within 5 years, or Colonoscopy within 10 years
  • Acute medical illness,
  • current GI bleed
  • history of adenomatous polyps
  • Colorectal Cancer
  • 1st degree relative with CRC \< age 60 years
  • inherited polyposis/non-polyposis syndrome
  • inflammatory bowel disease
  • Another household member enrolled in the study

Outcomes

Primary Outcomes

CRC screening completion rate

Time Frame: 12-14 Months

Rate of participants who receive CRC screening during study participation

Secondary Outcomes

  • Cost analysis of each intervention pathway(14 Months)

Study Sites (1)

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