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Clinical Trials/NCT03138304
NCT03138304
Completed
Not Applicable

Trial of a Video Game Intervention to Recalibrate Physician Heuristics: A Followup Study

University of Pittsburgh1 site in 1 country142 target enrollmentMay 2, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Wounds and Injuries
Sponsor
University of Pittsburgh
Enrollment
142
Locations
1
Primary Endpoint
Undertriage
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The objective of this study is to measure the duration of two different types of interventions to change physician decision making in trauma triage: a video game and an educational program.

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 developed an adventure video game (Night Shift) to serve as a novel method of recalibrating physician heuristics in trauma triage and compared its efficacy with a standard educational program. This study is designed to measure the degradation of the treatment effect.

Registry
clinicaltrials.gov
Start Date
May 2, 2017
End Date
June 1, 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

  • Physicians who care for adult patients in the Emergency Department.
  • Physicians who work at a non-trauma center.
  • Physicians who work at a Level III/IV trauma center.

Exclusion Criteria

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

Outcomes

Primary Outcomes

Undertriage

Time Frame: 6 months after completion of the intervention

Physicians in both arms of the study will be asked to complete an outcome assessment tool - a virtual simulation - six months after completion of their intervention. 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 calculate an under-triage rate for each physician (the number of simulated patients with severe injuries not transferred to a trauma center), will summarize the under-triage rate by group (Night Shift v. educational control), and will assess the difference in those rates.

Secondary Outcomes

  • Undertriage for nonrepresentative and representative injuries(6 months after completion of the intervention)
  • Degradation in treatment effect(6 months after completion of the intervention.)

Study Sites (1)

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