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Role of virtual reality technology in reducing pre-operative anxiety, stress and anaesthetic requirement in patients undergoing laparoscopic cholecystectomy

Role of virtual reality technology in reducing pre-operative anxiety, stress and anaesthetic requirement in patients undergoing laparoscopic cholecystectomy - A randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/073146
Enrollment
60
Registered
2024-08-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: K807- Calculus of gallbladder and bile duct without cholecystitis

Interventions

Intervention1: VIRTUAL REALITY TECHNOLOGY: a video will be shown to the patients through the virtual reality box to provide a visual and auditory experience for 15 minutes Control Intervention1: Simpl

Sponsors

Uttar Pradesh University Of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-40 years posted for elective laparoscopic cholecystectomy. 2. ASA physical status classification I and II.

Exclusion criteria

Exclusion criteria: 1. Patient refusal to participate in the study. 2. Having visual or auditory abnormalities. 3. H/o claustrophobia. 4. Chronic alcohol or substance addiction. 5. Motion sickness or vertigo. 6. H/o seizures. 7. Known case of adrenal insufficiency. 8. Cerebrovascular disease. 9. Previous history of any surgery.

Design outcomes

Primary

MeasureTime frame
To investigate the role of virtual reality in reducing pre operative anxiety levels in patients undergoing laparoscopic cholecystectomy under general anaesthesia using the Amsterdam preoperative anxiety and information scale (APAIS).Timepoint: Just before and after intervention

Secondary

MeasureTime frame
Hemodynamic parameters like heart rate, blood pressure and peripheral oxygen saturationTimepoint: just before and after the VR box intervention and every 15 minutes intra-operatively.;Post-operative pain will be assessed by using Visual analogue scale (VAS) scoreTimepoint: every 2 hourly, for the next 24 hours;Serum cortisol levelsTimepoint: just before the intervention and after the intervention .;The Bispectral Index value and the corresponding Minimum Alveolar Concentration valueTimepoint: every 15-minute interval intra-operatively.

Countries

India

Contacts

Public ContactDivya

UTTAR PRADESH UNIVERSITY OF MEDICAL SCIENCES , SAIFAI , ETAWAH

lucknow.manoj@gmail.com9410854970

Outcome results

None listed

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