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Clinical Trials in Turkey / NCT07425405
Recruiting Observational

Daily Screen Exposure and Preoperative Anxiety in Children Aged 2-5 Years

NCT07425405 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-03-11
Last updated
2026-03-12

Condition(s) studied

Preoperative Anxiety

Study summary

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.

Eligibility

Sex
ALL
Min age
2 Years
Max age
5 Years
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * Premedication administered or planned prior to anxiety assessment * Emergency surgical procedures * Known developmental delay or neurodevelopmental disorder * Known psychiatric disorder * Visual or hearing impairment that may interfere with behavioral assessment * Chronic use of sedative, antipsychotic, or antiepileptic medications * Anticipated need for postoperative intensive care * Incomplete or unreliable questionnaire data * Inability to perform mYPAS assessment prior to anesthesia induction

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital Istanbul küçükçekmece Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07425405 on ClinicalTrials.gov ↗ ← All trials in Turkey