Developing Strategies for Implementation and Use of the Operating Room Black Box (ORBB)
Part of paid clinical trials in Dallas, Texas.
- Sponsor
- University of Texas Southwestern Medical Center
- Study ID
- NCT06917183
- Status
- Not Yet Recruiting
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Conditions
- Demonstrate Effectiveness of Virtual Simulator in Improving OR Performance
Eligibility Criteria
- Sex
- ALL
- Age
- 20 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Training using the Immersive Multi- player Virtual Surgical Safety Checklist Training Simulator — OTHERTraining for performing surgical safety checklist for a period of 4 weeks.
Study Details
The goal of this study is to evaluate the current use of Operating Room Black Box (ORBB)data in order to develop simulation-based training that improves intraoperative outcomes and safety, and to assess barriers and facilitators to its implementation. There are 3 Aims for this study that the investigator will test, but the Aim that is the interventional portion of this study is only reported here in Aim 2 - Establish the validity and effectiveness of high-fidelity immersive virtual simulation-based training in improving operating room quality and safety.
Key Dates
- Start date
- Feb 1, 2027
- Status verified
- May 2026
- Primary completion
- Jun 30, 2028
- Completion
- Jun 30, 2028
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- No Intervention: Group 1: ControlGroup 1 participants will not receive any additional training except for instutionally mandated training
- Experimental: Group 2: SimulationGroup 2 will practice on the simulator one session every day for 4 weeks.
- Experimental: Group 3: Simulation with repeated reinforcementGroup 3 participants will practice on the simulator one session every day for 4 weeks and will continue to practice on the simulator once per week for an additional two months to a total of 8 sessions.
Primary Outcome Measure
Change in surgical safety checklist performance at 1 month post intervention [ Time Frame: Baseline, at one month post intervention ]
Central Contacts
- Ganesh Sankaranarayanan, PhD2067347458
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UT southwestern Medical Center | Dallas | Texas | 75390 | Ganesh Sankaranarayanan, PhD (PRINCIPAL_INVESTIGATOR) |