The efficacy of Distraction Technique to relieve pain in hospitalized childre
Not Applicable
- Conditions
- Pediatric painhoapitalization.C10.597.617E02.760.400
- Registration Number
- RBR-58jw26
- Lead Sponsor
- Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Data analysis completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Children aged between six and 12; who had language skills to communicate; in hospital context with different diagnoses; requiring prescribed venipuncture or arterial puncture by clinical demand; with time minimum of one day of hospitalization and time interval of no more than seven days between the puncture procedures.
Exclusion Criteria
Children with neurological impairments; children with communication problems; children under sedation.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expected outcome:<br>Pain intensity reduction (1), verified by Faces Pain Scale - Revised (FPS-R) (2), from the observation of a decrease at least two points in the post intervention measurement (3).<br><br>;Outcome found:<br>Pain intensity reduction (1), verified by Faces Pain Scale - Revised (FPS-R) (2), based on the statement of an average decrease of two points points in post intervention measurement (3).
- Secondary Outcome Measures
Name Time Method Expected outcome:<br>Reducing the intensity of pain (1), verified by the Visual Analog Scale of pain (VAS) (2), from the observation of a decrease of at least one point in the post intervention measurement (3).;Outcome found:<br>Pain intensity reduction (1), verified by the Visual Analog Scale of pain (VAS) (2), based on the statement of an average decrease of two points in the post intervention measurement (3).