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Recruiting NCT07495878

Educational Cartoon to Reduce Preoperative Anxiety in Children (CALM-KIDS)

No phase Interventional Pediatric Preoperative Anxiety

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Educational Cartoon, Distractor Cartoon, Standard Verbal Information.
Who it may be relevant to
Registry conditions: Pediatric Preoperative Anxiety. Basic parameters: 7 years — 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Watching a Preoperative Educational Cartoon on Anxiety in Children Aged 7 to 12 Years Undergoing Elective Procedures: A Prospective Randomized Controlled Trial

Overview

This prospective randomized controlled study aims to compare the effects of three preoperative information strategies on anxiety in children aged 7 to 12 years undergoing elective procedures under general anesthesia. Participants will be assigned to one of three groups: an educational cartoon group, a distractor cartoon group, or a standard verbal information group. In the educational cartoon group, children will watch a child-friendly cartoon prepared by the research team that explains the operating room environment, anesthesia, and the perioperative process. In the distractor cartoon group, children will watch an age-appropriate cartoon they already like, followed by standard verbal information. In the control group, children will receive standard verbal preoperative information only. The primary outcome is preoperative anxiety measured by the Modified Yale Preoperative Anxiety Scale (mYPAS) after the intervention and before induction of anesthesia. Secondary outcomes include the child's self-reported state anxiety measured by the State-Trait Anxiety Inventory for Children-State form (STAIC-State), parental anxiety and information requirement measured by the Amsterdam Preoperative Anxiety and Information Scale (APAIS), and perioperative vital signs. A total of 159 children will be enrolled at a single center.

Detailed description

Preoperative anxiety is common in children and may negatively affect cooperation, perioperative behavior, and the overall surgical experience. This study is designed to evaluate whether a child-friendly educational cartoon can reduce preoperative anxiety more effectively than a distractor cartoon or standard verbal information alone in children undergoing elective procedures under general anesthesia. The study is being conducted at a single center and is planned as a prospective randomized controlled clinical trial. A total of 159 pediatric patients aged 7 to 12 years will be enrolled, with 53 participants allocated to each study arm. 

Participants will be randomized into three groups. In Group 1, children will watch an educational cartoon entitled "Shuko Is Having Surgery," developed by the research team to explain preoperative preparation, induction of anesthesia, and the operating room environment in child-friendly language. In Group 2, children will watch an age-appropriate distractor cartoon previously preferred by the child; cartoon selection will exclude violent or frightening content and will be approved by the parent. In Group 3, no video will be shown and participants will receive routine standard verbal preoperative information only. Video viewing will last approximately 8 to 10 minutes and will be performed in the preoperative waiting area using the same device and environmental conditions. After video viewing, routine verbal information will also be provided according to standard practice. All children will receive oral midazolam 0.5 mg/kg as routine premedication approximately 20 to 30 minutes before video viewing or verbal information, using the same standardized protocol across all groups. 

The primary outcome measure is the child's preoperative anxiety level assessed with the Modified Yale Preoperative Anxiety Scale (mYPAS) at the preinduction period after completion of the assigned intervention. Secondary outcomes include the child's self-reported situational anxiety assessed by the State-Trait Anxiety Inventory for Children-State form (STAIC-State), parental preoperative anxiety and information requirement assessed by the Amsterdam Preoperative Anxiety and Information Scale (APAIS), and perioperative physiological parameters including heart rate, systolic and diastolic blood pressure, and oxygen saturation. These measures will be used to compare the effectiveness of the three information strategies and to explore the relationship between anxiety scores and physiological stress responses. 

Eligible participants are children aged 7 to 12 years scheduled for elective procedures under general anesthesia, classified as American Society of Anesthesiologists physical status I or II, whose parents provide written informed consent and who provide age-appropriate verbal assent. Exclusion criteria include a history of neurological or psychiatric disease, developmental delay or cognitive impairment, previous anesthesia experience, visual or hearing impairment preventing video viewing, and refusal of participation by the child or parent. Participation is voluntary, and withdrawal from the study will not affect medical care. Data will be recorded using coded identifiers only and stored securely with access limited to the research team.

Interventions

  • Behavioral Educational Cartoon
    A child-friendly educational cartoon prepared by the research team to explain preoperative preparation, anesthesia induction, the operating room environment, and equipment. The cartoon titled "Shuko Is Having Surgery" will be shown for approximately 8 to 10 minutes before surgery.
  • Behavioral Distractor Cartoon
    An age-appropriate cartoon previously preferred by the child and approved by the parent, selected to avoid violent or frightening content. The cartoon will be shown for approximately 8 to 10 minutes before surgery under standardized conditions.
  • Behavioral Standard Verbal Information
    Routine standard preoperative verbal information provided to the child about the surgical process, anesthesia, and the operating room environment according to institutional practice.

Primary outcome measures

  • Modified Yale Preoperative Anxiety Scale (mYPAS) Total Score [Time frame: Immediately after completion of the assigned intervention during the child's preinduction period, before induction of anesthesia]
Secondary outcome measures (3)
  • State-Trait Anxiety Inventory for Children-State Form (STAIC-State) Score [Time frame: Immediately after completion of the assigned intervention during the child's preinduction period, before induction of anesthesia]
  • Amsterdam Preoperative Anxiety and Information Scale (APAIS) Score [Time frame: Immediately after completion of the assigned intervention during the child's preinduction period, before induction of anesthesia]
  • Heart Rate [Time frame: During the child's preinduction period, before induction of anesthesia]

Eligibility criteria

Inclusion criteria

  • Children aged 7 to 12 years
  • Scheduled for an elective procedure under general anesthesia
  • American Society of Anesthesiologists (ASA) physical status I-II
  • Willingness of both the child and the parent to participate
  • Written informed consent from the parent and verbal assent from the child

Exclusion criteria

  • History of neurological or psychiatric disease
  • Developmental delay or cognitive impairment
  • Previous anesthesia experience
  • Visual or hearing impairment that would prevent watching the video
  • Inability to obtain parental consent or refusal of participation by the child

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • University of Health Sciences Gulhane Training and Research Hospital — Ankara

Identifiers

NCT: NCT07495878 · 2026/61

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗