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Clinical Trials/NCT05029219
NCT05029219CompletedNot Applicable

A Prospective Randomized Controlled Study for the Efficacy of Virtual Reality Intervention Procedure Simulator on the Training of Pain Procedures

Gangnam Severance Hospital1 site in 1 country20 target enrollmentStarted: August 31, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Checklist score

Study Overview

Brief Summary

The purpose of this study is to prove the effectiveness of the virtual reality program in educating lumbar transforaminal epidural blocks to novice doctors.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Residents in department of anesthesiology and pain medicine unfamiliar with fluoroscopy guided epidural block

Exclusion Criteria

  • Residents in department of anesthesiology and pain medicine familiar with fluoroscopy guided epidural block

Outcomes

Primary Outcomes

Checklist score

Time Frame: 60 min of education programs

When all training courses are completed and a post-test is performed on the phantom, it is determined how much the checklist score has changed compared to the screening time. Range from 0 to 7. Minimum score means worst and maximum score means good performance.

Secondary Outcomes

  • Global rating score(60 min of education programs)
  • Time taken to perform lumbar transforaminal epidural injection(Procedure duration)
  • Number of fluroscopy shots when performing lumbar transforaminal epidural injection under a fluoroscopy guide(Procedure duration)
  • Participants' satisfaction with the curriculum(60 min of education programs)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ji Yeong Kim

Assistant Professor

Gangnam Severance Hospital

Study Sites (1)

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