Effects of Cartoons and Mobile Games on Preoperative Anxiety and Fear in Children With Appendicitis: An RCT
Apandisit Tanısı Ile Cerrahi Servise Yatırılan Çocuklarda Preoperatif Kaygı ve Korkunun Azaltılmasında Çizgi Film ve Mobil Oyunların Etkisi: Randomize Kontrollü Bir Araştırma
his study aims to evaluate the effects of cartoon viewing and mobile game playing on preoperative anxiety and fear levels in children aged 7-12 years who are hospitalized for appendicitis surgery. The study is designed as a randomized controlled trial with three groups: a cartoon group, a mobile game group, and a control group receiving routine care.
Children in the intervention groups will watch a cartoon or play a mobile game for 10 minutes before surgery. Anxiety and fear levels will be measured using validated scales before and after the intervention. The findings of this study are expected to contribute to atraumatic care practices by providing simple and effective non-pharmacological methods to reduce preoperative anxiety and fear in children.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Preoperative anxiety and fear are common among children undergoing surgery and may negatively affect both perioperative outcomes and postoperative recovery. Non-pharmacological, atraumatic care interventions are recommended to minimize psychological distress in pediatric patients. Among these interventions, distraction techniques such as cartoon viewing and mobile game playing are widely used due to their practicality and accessibility.
This randomized controlled trial aims to compare the effects of cartoon viewing and mobile game playing on preoperative anxiety and fear levels in children aged 7-12 years diagnosed with appendicitis and admitted to a pediatric surgery unit. Participants will be randomly assigned to one of three groups: a cartoon intervention group, a mobile game intervention group, or a control group receiving routine care.
Children in the intervention groups will receive a 10-minute distraction intervention (cartoon viewing or mobile game playing) prior to surgery, while the control group will receive standard clinical care without any additional intervention. Anxiety and fear levels will be assessed before and after the intervention using validated measurement tools.
This study is expected to provide evidence-based data on the effectiveness of simple, low-cost, and easily applicable non-pharmacological interventions in reducing preoperative anxiety and fear in children. The findings may contribute to the development of atraumatic care practices and improve pediatric surgical care outcomes.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Eda Emine Yetkin, MSc Student
- Numéro de téléphone: +905 30 137 58 79
- E-mail: edaayetkinn@outlook.com
Lieux d'étude
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Ankara, Turquie (Türkiye)
- Recrutement
- Ankara Bilkent City Hospital
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Contact:
- Pediatric Surgery Service (4A and 4B Pediatric Surgery Service
- Numéro de téléphone: 0312 552 60 00
- E-mail: ankarasehir@saglik.gov.tr
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
Accepte les volontaires sains
La description
Inclusion Criteria:
- Being hospitalized in the Pediatric Surgery Service with a diagnosis of appendicitis.
- Being between the ages of 7 and 12 years.
- Voluntary consent/assent from both the child and their parents to participate in the study.
- Absence of any visual, auditory, or cognitive problems that prevent communication.
- Not having received any analgesics before the intervention.
Exclusion Criteria:
- Refusal to participate in the study voluntarily.
- Having a condition that prevents communication due to vision, hearing, speech, or mental health status.
- Being in an agitated state or unable to cooperate.
- Having received analgesics due to pain before the study.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Aucune intervention: Control Group
Participants in this group will receive standard hospital care and routine preoperative preparation without any additional digital distraction interventions.
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Expérimental: Cartoon Group
Participants in this group will be exposed to a cartoon-assisted distraction intervention designed to explain the surgical process and reduce anxiety before surgery.
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Participants will watch the cartoon titled "Şüko is Having Surgery," which explains the surgical process in child-friendly language, on an iPad Mini 6 with headphones for 10 minutes.
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Expérimental: Mobile Game Group
Participants in this group will engage in age-appropriate mobile games on a tablet computer as a digital distraction intervention prior to their surgical procedure.
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Children will be asked to play a game of their choice for 10 minutes on a tablet from among games selected according to their age group and PEGI standards (Head Ball 2, Subway Surfers, and Magic Tiles 3).
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Preoperative Anxiety Level
Délai: Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).
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The Modified Yale Preoperative Anxiety Scale (m-YPAS) will be used.
This scale provides an observational assessment across five categories (activity, emotional expressivity, state of arousal, vocalization, and use of parents).
Total scores range from 5 to 22, with higher scores indicating higher levels of anxiety.
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Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).
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Children's Fear Level
Délai: Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).
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The Children's Fear Scale (CFS) will be used.
This scale consists of five different facial expressions scored between 0 and 4. A score of 0 indicates "no anxiety/fear," whereas a score of 4 indicates "the highest level of fear."
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Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Heart Rate
Délai: Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
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The participants' heart rate will be measured to evaluate physiological stability.
The values will be recorded in beats per minute (bpm).
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Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
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Blood Pressure
Délai: Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
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The participants' systolic and diastolic blood pressure values will be measured.
The values will be recorded in millimeters of mercury (mmHg).
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Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
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Oxygen Saturation
Délai: Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
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The participants' peripheral oxygen saturation (SpO2) levels will be monitored.
The values will be recorded as a percentage (%).
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Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
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Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- TABED 1/1735/2025
- TYL-2026-2917 (Autre subvention/numéro de financement: Ankara Yildirim Beyazit University BAP Department)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
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