Comparison of distraction using virtual reality and augmented reality tools for reduction of anxiety of surgery in children.
Phase 4
- Conditions
- Health Condition 1: H662- Chronic atticoantral suppurative otitis mediaHealth Condition 2: N433- Hydrocele, unspecifiedHealth Condition 3: H028- Other specified disorders of eyelidHealth Condition 4: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2023/08/056014
- Lead Sponsor
- Maulana azad medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I-III.
Exclusion Criteria
1.Patients with injuries to head and face that would interfere in wearing headsets.
2. Skin infections and open wounds on face/head.
3. Inability to visualise AR/VR applications.
4. Patients in whom VR headsets do not fit appropriately.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in preoperative anxiety (mYPAS score).Timepoint: Baseline to induction.
- Secondary Outcome Measures
Name Time Method Change in preoperative anxiety using mYPAS score.Timepoint: during induction.;Parental anxiety using state trait anxiety inventory score. (STAI)Timepoint: after induction.;Parental satisfaction using parental & patient satisfaction scoresTimepoint: after induction;Pediatric induction compliance using induction compliance checklist score.Timepoint: During induction of general anaesthesia.;Time to central miosisTimepoint: after induction till central miosis;Time to loss of eyelash reflexTimepoint: after induction till loss of eyelash reflex