Psychological Distress
Conditions
Interventions
This is a two-arm, parallel, open-label, randomized controlled clinical trial. Experimental group: 175 children will use a Warrior VR Glass JS 3D virtual reality glasses, with images of the seabed dur
L01.224.160.875
Sponsors
Universidade Federal de Santa Catarina
Hospital Infantil Dr Jeser Amarante Faria
Eligibility
Age
4 Years to 15 Years
Inclusion criteria
Inclusion criteria: 4 to 15 years old, both genders; elective indication of venopuncture with catheter over needle; be aware; stable clinical or surgical conditions
Exclusion criteria
Exclusion criteria: cognitive deficit; diseases that affect pain sensitivity such as defects in neural tube formation; need for contact precautions; history of seizures; severe dehydration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that, from the use of virtual reality, there will be a reduction in the perception of pain in children undergoing peripheral intravenous catheterization, with lower values ??in the Faces Pain Scale-Revised, compared with the control group. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that, from the use of virtual reality, there will be an increase in the effectiveness of the success of peripheral intravenous catheterization, defined as: the insertion of the entire catheter in the first attempt, with blood return along the catheter cannula and infusion of 2 ml of Chloride 0.9% sodium, without changes in inspection and palpation of the insertion site, or painful complaints reported by the child, with the intravenous access device being able to receive fluids or medications (CUPER et al., 2012; AVELAR et al 2015). ; YEN et al, 2008) through the use of virtual reality in the child, verified through the increase of correct answers in the first attempt of catheterization.;it is expected that, from the use of virtual reality, there will be a reduction in the time to perform peripheral intravenous catheterization, through the use of virtual reality in the child, verified through the reduction of the time to perform the procedure.;A reduction in behavioral stress is expected, assessed through variables of the Observational Scale of Behavioral Distress, through the use of virtual reality in the child, verified through the greater frequency of the absence of the behaviors observed in this scale. | — |
Countries
Brazil
Contacts
Public ContactPatrícia Albeirice da Rocha
Universidade Federal de Santa Catarina
Outcome results
None listed