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Clinical Trials/NCT02330289
NCT02330289
Completed
Not Applicable

The Effect of Norms on Laboratory and Imaging Testing (ENLITen): a Pragmatic Randomized Controlled Trial

University of Pennsylvania0 sites154 target enrollmentDecember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Utilization
Sponsor
University of Pennsylvania
Enrollment
154
Primary Endpoint
Routine laboratory tests/patient-day
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Studies suggest that some laboratory tests ordered for hospitalized patients are duplicative or have limited value. This study will evaluate a normative feedback intervention to reduce overuse of laboratory tests for hospitalized patients by internal medicine physicians-in-training.

Detailed Description

Past research has shown that 25% of diagnostic testing is duplicative or has limited value. Academic medical centers that employ physicians-in-training may find it particularly challenging to reduce low value testing due to a historical emphasis on extensive workups by trainees. Despite the increased emphasis on cost-consciousness in medical education, there is little existing research evaluating ways to optimize ordering behaviors of physicians-in-training. This study will evaluate a normative feedback intervention for internal medicine physicians-in-training to reduce overuse of routine laboratory tests for hospitalized patients. Physicians-in-training will be cluster-randomized into two arms: (1) those who receive report cards (intervention group), (2) those who will not receive report cards (control group). We will study the use of routine laboratory tests over a pre-intervention period of 1 week and a post-randomization period of 1 week. We will study physician attitudes about the real-time feedback dashboard with qualitative assessments in focus groups after the completion of the intervention.

Registry
clinicaltrials.gov
Start Date
December 2015
End Date
September 2016
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kira Ryskina

Fellow, Division of General Internal Medicine

University of Pennsylvania

Eligibility Criteria

Inclusion Criteria

  • Any internal medicine physician-in-training scheduled to rotate through general medicine services at HUP during the study period will be included in the study.

Exclusion Criteria

  • Physicians-in-training pulled for weekend coverage or sick coverage will be excluded. Medical students will be excluded.

Outcomes

Primary Outcomes

Routine laboratory tests/patient-day

Time Frame: 6 months

the number of routine laboratory tests per patient-day ordered by the physicians-in-training

Secondary Outcomes

  • Laboratory costs(6 months)
  • Routine imaging tests/patient-day(6 months)
  • Physicians' attitudes toward laboratory test use and receiving feedback(6 months)

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