Pediatric Oncology.
Conditions
Interventions
Intervention 1: Intervention group: The group receiving intervention will commence the customary treatment that necessitates contact with a needle head, alongside virtual reality material in a distinc
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
3 Years to No maximum
Inclusion criteria
Inclusion criteria: Obtaining the consent of both children and their parents for participation in the study There are no issues with vision There are no problems with hearing There are no issues with speech The necessity of receiving an injection for medical treatment
Exclusion criteria
Exclusion criteria: Being below the age of three Being over the age of eighteen The child and their parents' lack of desire to participate in the study Having symptoms such as nausea and dehydration Use of sedatives Psychopathy Unstable state of physical or mental health
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: From the outset of the investigation. Method of measurement: Wong-Baker FACES (WBS) Pain Rating Scale and The Face, Legs, Activity, Cry and Consolability scale (FLACC).;Fear. Timepoint: From the outset of the investigation. Method of measurement: The Child Fear Scale (CFS).;Anxiety. Timepoint: From the outset of the investigation. Method of measurement: The Children’s Anxiety Meter-State (CAM-S). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHouriyeh Ehtemam
Kerman University of Medical Sciences
Outcome results
None listed