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Recruiting Observational

Effect of Daily Screen Time on Postoperative Emergence Delirium in Children Aged 2-11 Years

NCT07552896 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-05-01
Last updated
2026-08-05

Condition(s) studied

AgitationPostoperative Agitation

Investigational drug(s) / intervention(s)

Daily Screen Exposure Duration

Daily Screen Exposure Duration: This is a non-interventional observational study. The exposure of interest is the daily screen time duration of children aged 2-11 years, as reported by parents. Participants are categorized into two groups based on screen exposure (\<2 hours/day and \>2 hours/day). No active intervention is applied.

Study summary

This prospective observational study aims to evaluate the association between daily screen exposure duration and postoperative emergence delirium in children aged 2 to 11 years undergoing elective lower abdominal surgery. Daily screen time will be assessed using a parent-reported questionnaire administered preoperatively. Postoperative emergence delirium will be evaluated using the Pediatric Anesthesia Emergence Delirium (PAED) scale at 5, 10, 15, and 30 minutes after surgery.

The primary outcome is the association between daily screen time and PAED score within the first 30 minutes postoperatively. Secondary outcomes include the associations between PAED score and age at first screen exposure, type of viewed content, parental screen use, passive screen exposure, and the presence of a screen in the child's bedroom. The study is designed to improve understanding of whether screen-related environmental factors are associated with postoperative behavioral recovery in pediatric surgical patients.

Eligibility

Sex
ALL
Min age
2 Years
Max age
11 Years
Healthy volunteers
No
Inclusion Criteria: * Children aged 2 to 11 years * Scheduled for elective lower abdominal surgery * Planned procedures include inguinal hernia repair, orchiopexy for undescended testis, or circumcision * American Society of Anesthesiologists (ASA) physical status I-II * Parent or legal guardian able to provide written informed consent * Parent or legal guardian able to complete the study questionnaire Exclusion Criteria: * Planned or administered premedication before surgery * Emergency surgery * Reoperation * Developmental delay, neurodevelopmental disorder, or known psychiatric disease * Visual or hearing impairment that may interfere with behavioral assessment * Current use of sedative, antipsychotic, or antiepileptic medication * Anticipated postoperative intensive care unit requirement * Incomplete or unreliable parent-reported questionnaire data

Primary outcome measure(s)

  • Association Between Daily Screen Time and PAED Score — Within the first 30 minutes after emergence from anesthesia
    Correlation between daily screen exposure duration (continuous variable) and PAED score.

Trial sites (1)

FacilityCityRegionStatus
Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital Istanbul Istanbul Recruiting
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 NCT07552896 on ClinicalTrials.gov ↗ ← All trials in Turkey