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Clinical Trials in Turkey / NCT07297784
Enrolling by invitation Observational

Impact of Problematic Media Use on Postoperative Pain in Children Undergoing Tonsillectomy

NCT07297784 · tracked via the Priya Life Science Turkey tracker
Sponsor
Tokat Gaziosmanpasa University
Phase
Observational
Started
2026-01-01
Last updated
2026-06-26

Condition(s) studied

Adenotonsillectomy

Study summary

This observational study aims to investigate whether problematic media use is associated with postoperative pain severity in children aged 4-11 years undergoing tonsillectomy. A total of 94 parents who consent to participate and have children within the target age range will be included. Data will be collected using a structured questionnaire covering sociodemographic characteristics, family and child media habits, parental attitudes toward screen use, and the Problematic Media Use Scale (PMUS). Postoperative pain will be assessed using the FLACC scale at multiple time points within the first 24 hours after surgery.

Eligibility

Sex
ALL
Min age
4 Years
Max age
11 Years
Healthy volunteers
No
Inclusion Criteria: * Children aged 4-11 years * Scheduled for bilateral tonsillectomy * Parent/guardian capable of completing questionnaires * Parent/guardian willing to provide informed consent Exclusion Criteria: * Allergy, recent cold/upper respiratory infection * NSAID use within 24 hours before surgery * Any condition impairing pain assessment * Refusal of consent

Primary outcome measure(s)

  • FLACC pain scores — 1, 6, 12, and 24 hours postoperatively
    The FLACC (Face, Legs, Activity, Cry, Consolability) scale is a validated behavioral pain assessment tool used in pediatric patients who are unable to self-report pain reliably. It consists of five categories:Face, Legs, Activity, Cry, Consolability. Each category is scored from 0 to 2, resulting in a total score ranging from 0 to 10, where higher scores indicate more severe pain. Scores are interpreted as follows: 0: Relaxed and comfortable 1-3: Mild discomfort 4-6: Moderate pain 7-10: Severe pain or significant distress In this study, FLACC scores will be recorded at 1, 6, 12, and 24 hours postoperatively.

Trial sites (1)

FacilityCityRegionStatus
Tokat Gaziosmanpasa University Tokat Province Tokat Province

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Other trials for the same condition

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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 NCT07297784 on ClinicalTrials.gov ↗ ← All trials in Turkey