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Developing Strategies for Implementation and Use of the Operating Room Black Box (ORBB)

Developing Strategies for Implementation and Use of the Operating Room Black Box (ORBB)

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06917183
Enrollment
30
Registered
2025-04-08
Start date
2027-02-01
Completion date
2028-06-30
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Demonstrate Effectiveness of Virtual Simulator in Improving OR Performance

Keywords

Virtual Reality, Simulation, OR Team Performance

Brief summary

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.

Detailed description

The study will use a mixed within and between subjects' design with two groups - control, and simulation. Due to the dedicated time needed to enroll and complete the sessions along with the need for complete novice subjects, the investigator will recruit medical students at UT Southwestern Medical Center (UTSW) from all years for the simulation group. For the Control group, the investigator will recruit participants from our OR team with a minimum of 5 years of experience at Clements University Hospital (CUH) consisting of surgeons, residents, scrub techs, circulating nurses, anesthesiologists, Certified Registered Nurse Anesthetists (CRNAs) or first assists. Subjects will be randomized into either a control group (didactic) or experimental group (didactic with virtual simulation training). Pre-test: Both groups will take a knowledge assessment test (Multiple choice) that measures baseline knowledge in performing surgical safety checklist. Immediately after that, the participants will be asked to perform the surgical safety checklist once on the simulator. For uniform standard, all participants will choose the role of a surgeon. Both groups will then complete an online introductory module on surgical safety checklists that will be specifically created for use at UTSW. Subjects in the experimental group will then practice on the simulator for 8 sessions with each session not exceeding an hour. The 8 sessions will be completed within three weeks of the pre-test. Deliberate practice will be used to achieve satisfactory scores in the training. A total of 3 scenarios, which will be selected from expert inputs and align with institute priority, will be selected for the training. Post-test: At the end of three weeks, subjects from both groups will once again take the online knowledge test followed by performing the checklists on the simulator. Transfer test: One week after post-test, subjects from both groups will perform surgical safety checklists in a simulated operating room at the UTSW Simulation Center to assess predictive validity. For other team members during the transfer test, the investigator will use the research team and volunteers from the surgical service team. The transfer test performance will be videotaped for assessment.

Interventions

OTHERTraining using the Immersive Multi- player Virtual Surgical Safety Checklist Training Simulator

Training for performing surgical safety checklist for a period of 4 weeks.

Sponsors

University of Texas Southwestern Medical Center
Lead SponsorOTHER
Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

An immersive virtual reality simulator designed to teach how to properly perform surgical safety checklist.

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* OR service with a minimum of 5 years of experience that includes surgeons, residents, scrub techs, circulating nurses, anesthesiologists, CRNAs or first assists

Exclusion criteria

* OR team members (surgeons, scrub techs, circulating nurses, anesthesiologists, CRNAs or first assists) with less than 5 years of experience

Design outcomes

Primary

MeasureTime frameDescription
Change in surgical safety checklist performance at 1 month post interventionBaseline, at one month post interventionChange in surgical safety checklist performance is assessed using the Compliance, engagement and quality scores computed automatically using the ORBB
Change in surgical safety checklist performance at 3 months post interventionBaseline, at 3 months post interventionChange in surgical safety checklist performance is assessed using the Compliance, engagement and quality scores computed automatically using the ORBB
Change in surgical safety checklist performance at 5 months post interventionBaseline, at 5 months post interventionChange in surgical safety checklist performance is assessed using the Compliance, engagement and quality scores computed automatically using the ORBB

Countries

United States

Contacts

CONTACTGanesh Sankaranarayanan, PhD
Ganesh.Sankaranarayanan@UTSouthwestern.edu2067347458
PRINCIPAL_INVESTIGATORGanesh Sankaranarayanan, PhD

University of Texas Southwestern Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026