Anxiety
Conditions
Interventions
Control group: 45 patients (4-14 years old) who do not have hearing, visual or cognitive impairments will be submitted to conventional venous anesthetic induction with venipuncture. Using the Modified
L01.224.160.875
Sponsors
Faculdade de Medicina de Botucatu
Faculdade de Medicina de Botucatu
Eligibility
Age
4 Years to 14 Years
Inclusion criteria
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
Exclusion criteria: Hearing deficiency; Visual impairment; intellectual disability
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactCarolina Cruz
Faculdade de Medicina de Botucatu
Outcome results
None listed