Wounds and Injuries Clinical Trial
Official title:
A Randomized Controlled Trial of a Video Game Intervention to Recalibrate Physician Heuristics
| Verified date | August 2017 |
| Source | University of Pittsburgh |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The objective of this study is to compare the efficacy of a video game designed to recalibrate physician heuristics in trauma triage with a standard educational program.
| Status | Completed |
| Enrollment | 368 |
| Est. completion date | November 2016 |
| Est. primary completion date | November 2016 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | N/A and older |
| Eligibility |
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 at a Level I/II trauma center. - Physicians who do not practice in the US. |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| University of Pittsburgh | Carnegie Mellon University |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Under-triage rate | Physicians in both arms of the study will be randomized to complete one of two versions of a virtual simulation: a control version and a cognitive load version. They will complete the 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 calculate an under-triage rate for each physician (the number of simulated patients with severe injuries not transferred to a trauma center), summarize the under-triage rate by group (Night Shift v. educational control), and will compare the difference in those rates. |
After completion of the intervention | |
| Secondary | The effect of cognitive load on the under-triage rate | As described above, participants will complete either a control or cognitive load version of the virtual simulation upon completion of the intervention, ideally within one month of the enrollment. As a secondary outcome measure, the investigators will assess the difference in under-triage rates of physicians who complete the simulation under control and cognitive load conditions, by intervention type. | After completion of the intervention |
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