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Clinical Trials/NCT00793455
NCT00793455
Completed
Not Applicable

Using Precision Performance Measurement To Conduct Focused Quality Improvement. Sub-Study 1.

Northwestern University1 site in 1 country628 target enrollmentOctober 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Cancer Screening
Sponsor
Northwestern University
Enrollment
628
Locations
1
Primary Endpoint
Colorectal Cancer Screening Completion.
Status
Completed
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 preventive screenings ordered by their physician. We hypothesize that educational outreach may increase completion rates.

Detailed Description

We designed an intervention to focus on patients who have received and accepted a referral for colonoscopy, yet have exhibited some barriers to screening as demonstrated by a lack of screening completion. We conducted a randomized controlled trial to assess the effects of a multicomponent intervention (patient reminder, print and multimedia materials) on colorectal screening completion among this target population.

Registry
clinicaltrials.gov
Start Date
October 2008
End Date
November 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's physician has ordered a preventive screening test
  • Patient has not completed this test in 3 months
  • Patient of Northwestern Medical Faculty Foundation General Internal Medicine Clinic.

Exclusion Criteria

  • Patient has been given a more recent order for the same screening test.
  • Patient has significant life stress as noted in the Electronic Health Record (EHR)

Outcomes

Primary Outcomes

Colorectal Cancer Screening Completion.

Time Frame: 3 months post randomization

We reviewed electronic health records of participants 3 months post randomization to ascertain outcome. We looked for one or both of the following (1) note in free text MD note documenting receipt of one form of colorectal cancer (CRC) screening during study period (2)lab results from fecal occult blood test, sigmoidoscopy, or colonoscopy. Participants were categorized as completing CRC screening if there was a lab result or physician note located in chart during study period. If no note or lab result was found in chart, then the participant was categorized as not completing CRC screening.

Secondary Outcomes

  • Colorectal Cancer Screening Completion(6 months post randomization)

Study Sites (1)

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