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N/A N=8 Randomized Prevention

Translation of Colorectal Cancer Screening Guidelines to Practice: A System Intervention

Colorectal Cancer

Enrolled (actual)
8
Serious AEs
Results posted
Jan 2014
Primary outcome: Primary: Percent of Patients Receiving GI Consult for FOBT+ Results — 39; 47; 64; 51 percent patients receiving GI consult

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Electronic Consult System (Device)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
US Department of Veterans Affairs
Primary completion
May 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Percent of Patients Receiving GI Consult for FOBT+ Results
39; 47; 64; 51; 68; 80
PRIMARY
Percent of Patients Receiving GI Consult Plus Anatomic Workup for FOBT+ Results
4; 12; 19; 4; 30; 21

Summary

Colorectal cancer (CRC) is the second leading cause of cancer-related deaths in the United States. Results from randomized clinical trials and intervention studies have suggested that implementation of a CRC screening program for men and women over age 50 results in reduced CRC mortality. However, for this reduction to be fully realized, it is imperative that all positive screening tests are followed by complete diagnostic evaluation (CDE). Numerous intervention programs have been used to improve initial CRC screening rates, but data indicate that outside the research setting, less than half of patients with a positive fecal occult blood test (FOBT) screening result undergo CDE. To enhance the translation of this best practice recommendation to clinical practice, the investigators propose to implement an electronic event notification intervention (CRC-ENS) directed at making physician and system level changes to increase the proportion of patients with an abnormal FOBT that undergo CDE.

Eligibility Criteria

Inclusion Criteria

  • VA Medical Centers with either CORI (Clinical Outcomes Research Initiative) or electronic notes/descriptions documenting GI endoscopic procedures

Exclusion Criteria

  • VA Medical Centers without electronic GI procedure documentation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00122187). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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