Investigating the capability of virtual reality to relieve pain, fear, and anxiety experienced by pediatric oncology patients during needle insertion: A clinical trial
Not Applicable
Recruiting
- Conditions
- Pediatric Oncology.
- Registration Number
- IRCT20210710051836N2
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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).
- Secondary Outcome Measures
Name Time Method