The Effectiveness of an Interventional-Supportive Program on Children's Anxiety and Pai
Not Applicable
- Conditions
- Pediatric surgery ?.
- Registration Number
- IRCT20191004044976N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
3 to 6 year old children
Having mental health and consciousness
Surgery on the gastrointestinal
Children whose hospitalization is longer than two days after surgery
Exclusion Criteria
Taking anti anxiety drugs
Having growth and mental retardation
Having a history of chronic illness (epilepsy, seizures, diabetes, diagnosed heart disease, kidney disease)
Previous surgical experience
Taking anti pain drugs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before intervention, One hour After intervention. Method of measurement: Toddler-Preschool-Post operative scale(TPPPS).;Anxiety. Timepoint: Before intervention, One hour After intervention. Method of measurement: Piyeri's Self-report tool for severity of anxiety.
- Secondary Outcome Measures
Name Time Method