Effect of Videogames on Real-life Triage Patterns
- Conditions
- Physician's RoleTrauma
- Interventions
- Behavioral: Video games
- Registration Number
- NCT04516044
- Lead Sponsor
- University of Pittsburgh
- Brief Summary
In 2016 and 2017 the investigators conducted two clinical trials in which emergency medicine physicians were randomized either to an intervention (customized, theoretically-based video games) or to a control (nothing or text-based education). This study will now assess long-term outcomes for physicians enrolled in those two trials to evaluate the effect of the interventions on triage practices for trauma patients who presented initially to non-trauma centers in the US between December 2016 and November 2018.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 686
- Participated in two prior clinical trials (Physician)
- ≥65 years old (Patient)
- enrolled in Medicare fee-for-service
- sustained a moderate-severe injury (i.e. ISS [injury severity score] >15) (Patient)
- treated by physician enrolled in prior clinical trials (Patient)
- Did not participate in two prior clinical trials (Physician)
- <65 years old (Patient)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Video game Video games Patients treated by physicians who were randomized to either play an adventure-based video game that used narrative engagement to recalibrate physician heuristics in trauma triage or a puzzle-based video game that used analogical encoding to recalibrate physician heuristics in trauma triage.
- Primary Outcome Measures
Name Time Method Number of patients triaged to trauma centers 1 year following the intervention The investigators will use Medicare claims to measure the number of patients, treated by study participants, who present initially to non-trauma centers after a moderate-severe injury and are transferred to a Level I/II trauma center during that episode of care. They will compare triage patterns for patients treated by physicians in the intervention and in the control groups.
- Secondary Outcome Measures
Name Time Method Number of moderate-severely injured patients who die 30-days after initial evaluation 1 year following the intervention Patient mortality 30-days after evaluation for a moderate-severe injury by a physician enrolled in the trial, compared among intervention and control groups.
Frequency of resources used for patients with moderate-severe injuries treated by participants 1 year following intervention Frequency of resources used (e.g. ICU admission, mechanical ventilation, disposition status) after initial presentation for a moderate-severe injury and treatment by a participating physician, compared among intervention and control groups.
Trial Locations
- Locations (1)
University of Pittsburgh
🇺🇸Pittsburgh, Pennsylvania, United States