Evaluate the effect of using Virtual Reality on anesthetic induction in childre

Not Applicable

• Conditions: R52.0; Anxiety

• Registration Number: RBR-7z8kn4k
• Lead Sponsor: Faculdade de Medicina de Botucatu

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-05-25
• Last Update Posted: 29 May 2023
• Study Completion: 2024-03-01

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Pediatric patients aged 4 to 14 years; both sexes; non-carriers of hearing, visual or cognitive disabilities; who will undergo anesthetic induction

Exclusion Criteria

Hearing deficiency; Visual impairment; intellectual disability

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
From a pilot project developed with 8 patients, an estimated difference of 20% is expected in the assessment of anxiety using the Modified Yale Preoperative Anxiety Scale - EAPY-m and the assessment of pain using the Revised Faces Scale ( FPS-R) and Visual Analogue Scale (VAS) between groups. Considering a test power of 90% and a significance level of 5%, the sample size was defined as 45 patients in each of the groups.

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected.