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Using Virtual Reality to Help Reduce Anxiety in People Having Orthopedic Surgery

Effect of Immersive Virtual Reality (IVR) on intraoperative anxiety in patients undergoing Orthopedic Surgeries under Regional Anaesthesia: A randomized control study. - IVRA-RA

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085541
Enrollment
60
Registered
2025-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: VR Group:participants will receive an immersive virtual reality (IVR) experience using an Oculus Quest VR headset with earphones: After shifting the patient to the operation theatre and

Sponsors

AIIMS Bhopal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: adults aged 18 years and older with an American Society of Anesthesiologists (ASA) physical status classification of I or II who are undergoing orthopedic surgeries- 1. under brachial plexus block for upper limb 2. neuraxial anaesthesia for lower limb surgery

Exclusion criteria

Exclusion criteria: 1.patients declining participation 2.those with cognitive impairments 3.a history of epilepsy, psychosis, or claustrophobia 4.individuals with sensory impairments (blindness, deafness), and those unwilling to use the VR headset if applicable. 5.Cases will be excluded if we need to convert the anaesthesia to GA on account of prolonged duration

Design outcomes

Primary

MeasureTime frame
Anxiety levels assessed using Visual Analog Scale for Anxiety (VAS-A) [13] at specified time points: 1. Baseline (1 day pre-surgery) 2. Pre-operative room (prior to transfer to the operating theatre) 3. 30 minutes after the start of surgery and anaesthesia induction 4. Post-surgery in the recovery roomTimepoint: Anxiety levels assessed using Visual Analog Scale for Anxiety (VAS-A) [13] at specified time points: 1. Baseline (1 day pre-surgery) 2. Pre-operative room (prior to transfer to the operating theatre) 3. 30 minutes after the start of surgery and anaesthesia induction 4. Post-surgery in the recovery room

Secondary

MeasureTime frame
Requirement for additional sedation (total top-up doses of midazolam 0.02mg/kg in VR Group) 2. Hemodynamic changes (blood pressure, heart rate) 3. Patient satisfaction levels with anaesthesia and overall care measured by a satisfaction questionnaire, which will measured by a Likert scale after completing the surgical procedure. 4. Side effects for example- nausea, vomiting, headache, asthenopia 5. Postoperative Care Unit Stay Duration (patient will be shifted on achieving Aldrete score of 9).Timepoint: Specified time points- 30 minutes after the start of surgery and anaesthesia induction Post-surgery in the recovery room

Countries

India

Contacts

Public ContactDr Shikha Jain

All India Institute Of Medical Sciences (AIIMS), Bhopal

shikha.anaesth@aiimsbhopal.edu.in07987164388

Outcome results

None listed

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