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The application of Virtual Reality in Lumbar Transforaminal Epidural Steroid Injection: a randomised controlled trial

The application of Virtual Reality in Lumbar Transforaminal Epidural Steroid Injection: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093450
Enrollment
Unknown
Registered
2024-12-05
Start date
2024-12-16
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Lumbar disc herniation with radicular symptoms

Interventions

Virtual reality group:Learners practice TFESI on the VR -based surgical trainer
Traditional group:Learners practice TFESI on the normal model

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Have not undergone TFESI surgery; (2) Have not experienced TFESI related training; (2) Signed informed consent.

Exclusion criteria

Exclusion criteria: (1)One already had participated in training related with VR; (2)One have motion sickness or Vertigo.

Design outcomes

Primary

MeasureTime frame
Duration of puncture;—

Secondary

MeasureTime frame
Global rating scale;Puncture success rate;Simulative number of radiations;Teaching satisfaction ratings;—

Countries

China

Contacts

Public ContactYe Ling

Department of Pain Management, West China Hospital, Sichuan University

Zerodq-hx@163.com+86 189 8060 1894

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026