Actively Recruiting
Daily Screen Exposure and Preoperative Anxiety in Children Aged 2-5 Years
Led by Kanuni Sultan Suleyman Training and Research Hospital · Updated on 2026-03-12
275
Participants Needed
1
Research Sites
24 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective observational study aims to evaluate whether daily screen exposure duration is associated with preoperative anxiety levels in children aged 2-5 years undergoing elective surgery. Screen exposure in early childhood has been associated with emotional and behavioral outcomes, including increased anxiety. However, its potential impact on anxiety in acute stress situations such as surgery has not been previously investigated. Preoperative anxiety in children is associated with difficult anesthetic induction, increased postoperative agitation, prolonged recovery, and behavioral disturbances. In this study, parents will complete a structured questionnaire assessing their child's daily screen exposure duration and related factors. Children will be categorized into three groups according to reported daily screen time: less than 1 hour per day, 1-2 hours per day, and more than 2 hours per day. Preoperative anxiety will be assessed immediately before anesthesia induction using the Modified Yale Preoperative Anxiety Scale (mYPAS), a validated observational tool for measuring anxiety in young children. No additional medical interventions will be performed beyond routine clinical care. The study seeks to determine whether higher screen exposure is associated with increased preoperative anxiety levels and to identify potential risk factors contributing to anxiety in preschool children undergoing surgery.
CONDITIONS
Official Title
Daily Screen Exposure and Preoperative Anxiety in Children Aged 2-5 Years
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 2 to 5 years
- Scheduled for elective surgical procedures under general anesthesia
- American Society of Anesthesiologists (ASA) physical status I-III
- Parent or legal guardian able to provide written informed consent
- Parent able to complete the structured questionnaire in Turkish
You will not qualify if you...
- Premedication administered or planned before anxiety assessment
- Emergency surgical procedures
- Known developmental delay or neurodevelopmental disorder
- Known psychiatric disorder
- Visual or hearing impairment affecting behavioral assessment
- Chronic use of sedative, antipsychotic, or antiepileptic medications
- Expected need for postoperative intensive care
- Incomplete or unreliable questionnaire data
- Unable to perform mYPAS assessment before anesthesia induction
AI-Screening
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Trial Site Locations
Total: 1 location
1
Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital
Istanbul, küçükçekmece, Turkey (Türkiye), 34303
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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