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Clinical Trials/IRCT20230219057451N1
IRCT20230219057451N1
Completed
Phase 3

Effects of Immersive Virtual Reality on patient anxiety during surgery under regional anesthesia: A randomized clinical trial

Diponegoro University0 sites30 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Healthy Subject.
Sponsor
Diponegoro University
Enrollment
30
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Diponegoro University

Eligibility Criteria

Inclusion Criteria

  • Male and female aged 18\-50 years
  • Graduated from high school/equivalent
  • American Society of Anesthesiologists (ASA) physical status I\-II
  • Patients who are going to have lower abdominal or lower extremity surgery under regional anesthesia combined with spinal epidural neuraxial block
  • No previous surgery history
  • No history of epilepsy, psychiatric disorders, or claustrophobia and having visual acuity \> 6/60
  • Patients with moderate to severe anxiety scores (Spielberger state\-trait anxiety inventory \[STAI] score \> 38\)

Exclusion Criteria

  • Patients with shock or other major anesthetic or surgical complications during the procedure
  • Patients who refused to participate in the study
  • Regional anesthetic needle insertion \>2 times
  • VR device (Oculus Quest VR) that is damaged or error during the surgery process
  • Patients who dropped out of this study

Outcomes

Primary Outcomes

Not specified

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