NCT06063434

Brief Summary

The goal of this clinical trial is to test the effect of a video game on the implementation of clinical practice guidelines in trauma triage. The main question it attempts to answer is whether exposure to the game improves compliance with guidelines by emergency medicine physicians working at non-trauma centers in the US. Participants randomized to the intervention condition will be asked to play a customized, theory-based video game for 2 hours immediately after enrollment, and then return to the game for 20 minutes every three months for the next 9 months. Participants in the control condition will receive usual care.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
800

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 20, 2023

Completed
12 days until next milestone

First Posted

Study publicly available on registry

October 2, 2023

Completed
2 months until next milestone

Study Start

First participant enrolled

November 27, 2023

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2025

Completed
1.1 years until next milestone

Results Posted

Study results publicly available

May 6, 2026

Completed
Last Updated

May 6, 2026

Status Verified

May 1, 2026

Enrollment Period

1.3 years

First QC Date

September 20, 2023

Results QC Date

March 30, 2026

Last Update Submit

May 5, 2026

Conditions

Keywords

HeuristicsSerious gameGuidelines

Outcome Measures

Primary Outcomes (1)

  • Under-triage

    Number of severely injured patients, treated by trial participants, who are admitted or discharged (i.e., not transferred) after initial evaluation at a non-trauma center as recommended by clinical practice guidelines.

    1 year

Secondary Outcomes (3)

  • Mortality and Hospital Readmission

    1 year

  • Functional Dependence

    1 year

  • Over-triage

    1 year

Study Arms (2)

Night Shift

EXPERIMENTAL

Night Shift 2024 is a customized, theory-based adventure video game in which the player takes on the character of Andy Jordan, a young emergency medicine physician who moves home after the disappearance of his grandfather and takes a job at a local community hospital. The investigators will ask participants to play Night Shift for 2 hours upon enrollment (or within 2 weeks), and then come back to the game quarterly to play it again for 20 minute booster sessions. They will unlock additional game content each quarter to make the experience more enjoyable.

Behavioral: Night Shift

Usual education

ACTIVE COMPARATOR

Participants will receive their usual continuing medical education, but nothing additional.

Behavioral: Usual education

Interventions

Night ShiftBEHAVIORAL

The player must not only manage the patients who present to the emergency department of the hospital, gaining experience with the consequences of trauma triage, but also solve the mystery of the grandfather, gaining an emotional connection with the character and making the feedback that "Andy" receives more relevant. Embedded within Night Shift 2024 is a mini-game (Graveyard Shift) that contains a series of puzzles that reinforce the lessons of the overarching game: transfer severely injured patients expeditiously.

Night Shift
Usual educationBEHAVIORAL

Standard continuing medical education, including Advanced Trauma Life Support, and the American Board of Emergency Medicine educational modules (e.g., trauma resuscitation).

Usual education

Eligibility Criteria

Age25 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \- Board certified physicians who work exclusively in the emergency departments (EDs) of non-trauma centers in the US AND triage adult trauma patients

You may not qualify if:

  • non-physician healthcare professionals who work in EDs
  • physicians who work at trauma and non-trauma centers
  • physicians who work outside the continental US

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Pittsburgh

Pittsburgh, Pennsylvania, 15213, United States

Location

Related Publications (3)

  • Mohan D, Chang CH, Fischhoff B, Elmer J, Rak KJ, Barnes JL, Peitzman AB, Bendesky B, Carr C, Chapman AC, Forsythe RM, Guyette FX, Hynes AM, Oskvarek JJ, Weingart SD, Weinstock MB, White DB, Angus DC. Using Serious Games to Increase the Implementation of Trauma Triage Guidelines: A Randomized Clinical Trial. JAMA. 2026 Apr 20. doi: 10.1001/jama.2026.4079. Online ahead of print.

  • Mohan D, Fischhoff B, Talisa V, Elmer J, White DB, Angus DC, Peitzman A, Bendesky B, Chapman AC, Forsythe RM, Guyette FX, Hynes AM, Oskvarek JJ, Weingart SD, Weinstock M, Chang CH. An Educational Video Game in Trauma Triage at Nontrauma Centers: A Secondary Analysis of a Randomized Clinical Trial. JAMA Netw Open. 2025 Jun 2;8(6):e2513375. doi: 10.1001/jamanetworkopen.2025.13375.

  • Mohan D, Angus DC, Chang CH, Elmer J, Fischhoff B, Rak KJ, Barnes JL, Peitzman AB, White DB. Using a theory-based, customized video game as an educational tool to improve physicians' trauma triage decisions: study protocol for a randomized cluster trial. Trials. 2024 Feb 16;25(1):127. doi: 10.1186/s13063-024-07961-w.

MeSH Terms

Conditions

Accidental Injuries

Interventions

Shift Work Schedule

Condition Hierarchy (Ancestors)

Wounds and Injuries

Intervention Hierarchy (Ancestors)

Personnel Staffing and SchedulingPersonnel ManagementOrganization and AdministrationHealth Services Administration

Limitations and Caveats

1. We used Medicare Fee-for-Service 2. We used claims for outcome assessment 3. We assigned process of care to the individual physician, but recognize the complex contextual nature of trauma triage 4. We provided a material incentive to encourage task completion 5. Although missingness of data was low, we cannot exclude a small residual bias. 6. Our public protocol disclosed block sizes of 4 or 6, creating a theoretical risk of allocation prediction.

Results Point of Contact

Title
Dr. Deepika Mohan
Organization
University of Pittsburgh

Study Officials

  • Deepika Mohan, MD

    University of Pittsburgh

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Participant assignment will be masked within the data with unblinding occurring only after data cleaning has completed.
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Physicians will be randomized in a 1:1 fashion to the intervention condition or to the control condition.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

September 20, 2023

First Posted

October 2, 2023

Study Start

November 27, 2023

Primary Completion

March 30, 2025

Study Completion

March 30, 2025

Last Updated

May 6, 2026

Results First Posted

May 6, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will share

The protocol, primary data, and meta-data (e.g., documentation, protocols used to clean and to manage the data), will be uploaded to the open access Inter-university Consortium for Political and Social Research (open ICPSR) repository at the conclusion of the trial. Of note, data obtained from Medicare will not be shared as part of the results of the trial, because we do not own those records.

Shared Documents
STUDY PROTOCOL, SAP, ANALYTIC CODE
Time Frame
6 months after publication of the primary manuscript.
Access Criteria
We will upload the data to the open ICPSR repository, where other researchers can access it.

Locations