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 — OTHER
    Training 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: Control
    Group 1 participants will not receive any additional training except for instutionally mandated training
  • Experimental: Group 2: Simulation
    Group 2 will practice on the simulator one session every day for 4 weeks.
  • Experimental: Group 3: Simulation with repeated reinforcement
    Group 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

Locations (1)

FacilityCityStateZIPSite coordinators
UT southwestern Medical CenterDallasTexas75390
Ganesh Sankaranarayanan, PhD
2067347458
Ganesh Sankaranarayanan, PhD (PRINCIPAL_INVESTIGATOR)

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