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Clinical Trials/NCT00860249
NCT00860249
Terminated
Not Applicable

Using Precision Performance Measurement To Conduct Focused Quality Improvement. Sub-study 2

Northwestern University1 site in 1 country60 target enrollmentMarch 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Cancer
Sponsor
Northwestern University
Enrollment
60
Locations
1
Primary Endpoint
Completion of CRC Screening
Status
Terminated
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to evaluate whether patient outreach is effective at increasing compliance with preventative screenings for those patients who, based on national quality standards, have become newly eligible for screening measures. We hypothesize that educational outreach may increase completion rates.

Registry
clinicaltrials.gov
Start Date
March 2009
End Date
December 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kenzie Cameron

Research Associate Professor

Northwestern University

Eligibility Criteria

Inclusion Criteria

  • Patient of Northwestern Medical Faculty Foundation General Internal Medicine
  • Patient has a scheduled appointment with a GIM physician in the next several weeks
  • Patient will be 50 years old at the time of this appointment
  • Patient is male or female

Exclusion Criteria

  • This is the first time the patient is seen in the NMFF GIM clinic
  • There is a prior completion of CRC screening noted in EHR.
  • There is a prior order placed for CRC screening in EHR.
  • Patient has a history of CRC
  • Patient has a diagnosis of ulcerative colitis, inflammatory bowel disease, Crohn's Disease, or documented colectomy.

Outcomes

Primary Outcomes

Completion of CRC Screening

Time Frame: 6 months from initial contact

What would have been reported as this Outcome Measure is the number of participants who completed screening. We planned to review electronic health records of participants 6 months post randomization to look for either: (1) note in free text MD note documenting receipt of one form of colorectal cancer (CRC) screening during study period or (2)lab results from fecal occult blood test, sigmoidoscopy, or colonoscopy. Screening completion equaled presence of a lab result or physician note in chart. No patient charts were reviewed due to low accrual.

Secondary Outcomes

  • The Secondary Outcome for the Study is the Time to Screening Completion.(6 months after randomization)

Study Sites (1)

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