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Clinical Trials/NCT03279575
NCT03279575
Completed
N/A

Testing the Efficacy of Two Behavioral Interventions at Recalibrating Physician Heuristics in Trauma Triage: a Randomized Clinical Trial

University of Pittsburgh1 site in 1 country320 target enrollmentOctober 29, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Wounds and Injuries
Sponsor
University of Pittsburgh
Enrollment
320
Locations
1
Primary Endpoint
Incidence rate of successful triage
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The objective of this study is to compare the efficacy of two behavioral interventions at recalibrating physician heuristics.

Detailed Description

Treatment at trauma centers improves outcomes for patients with moderate-to-severe injuries. Accordingly, professional organizations, state authorities, and the federal government have endorsed the systematic triage and transfer of these patients to trauma centers either directly from the field or after evaluation at a non-trauma center. Nonetheless, between 30 to 40% of patients with moderate-to-severe injuries still only receive treatment at non-trauma centers, so-called under-triage. Most of this under-triage occurs because of physician decisions (rather than first-responder decisions). Existing efforts to change physician decision making focus primarily on knowledge of clinical practice guidelines and attitudes towards the guidelines. These strategies ignores the growing consensus that decision making reflects both knowledge as well as intuitive judgments (heuristics). Heuristics, mental short cuts based on pattern recognition, drive the majority of decision making. The investigators have developed two separate behavioral interventions to recalibrate physician heuristics in trauma triage, and will compare the effect of these interventions, an educational program, and no intervention on physician performance on a virtual simulation.

Registry
clinicaltrials.gov
Start Date
October 29, 2017
End Date
December 11, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Deepika Mohan

Assistant professor of critical care medicine

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • Emergency medicine physicians who work at a non-trauma center.
  • Emergency medicine physicians who work at a Level III/IV trauma center.

Exclusion Criteria

  • Emergency medicine physicians who work only at a Level I/II trauma center.
  • Emergency medicine physicians who do not practice in the US.

Outcomes

Primary Outcomes

Incidence rate of successful triage

Time Frame: One month after completion of the intervention

Physicians in all arms of the study will be asked to complete a virtual simulation, upon completion of the intervention, ideally within one month of enrollment. The virtual simulation replicates the environment of the ED. Physicians have to manage 10 patients that appear concurrently, while also responding to a series of audio-visual distractors. Specifically, they must provide information on whether they will admit, transfer, or discharge the patients home. The investigators will categorize severely injured patients as successfully transferred (transferred to a trauma center or died in the ED) or not (admitted). We will use a Poisson regression to estimate the association between successful transfer and exposure to the different interventions (Night Shift v. Graveyard Shift v. educational program v. control).

Study Sites (1)

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