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Effects of Cartoons and Mobile Games on Preoperative Anxiety and Fear in Children With Appendicitis: An RCT

2026年6月8日 更新者:Ankara City Hospital Bilkent

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.

研究概览

详细说明

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.

研究类型

介入性

注册 (估计的)

69

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子

接受健康志愿者

不

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
无干预:Control Group
Participants in this group will receive standard hospital care and routine preoperative preparation without any additional digital distraction interventions.
实验性的: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.
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.
实验性的: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.
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).

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Preoperative Anxiety Level
大体时间:Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).
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.
Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).
Children's Fear Level
大体时间:Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).
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."
Baseline (upon admission to the pediatric surgery inpatient unit prior to the intervention) and post-intervention (immediately before transfer to the operating room).

次要结果测量

结果测量
措施说明
大体时间
Heart Rate
大体时间:Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
The participants' heart rate will be measured to evaluate physiological stability. The values will be recorded in beats per minute (bpm).
Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
Blood Pressure
大体时间:Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
The participants' systolic and diastolic blood pressure values will be measured. The values will be recorded in millimeters of mercury (mmHg).
Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
Oxygen Saturation
大体时间:Measured at two time points: baseline (pre-intervention) and immediately post-intervention.
The participants' peripheral oxygen saturation (SpO2) levels will be monitored. The values will be recorded as a percentage (%).
Measured at two time points: baseline (pre-intervention) and immediately post-intervention.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年10月10日

初级完成 (估计的)

2026年5月30日

研究完成 (估计的)

2026年5月30日

研究注册日期

首次提交

2026年5月6日

首先提交符合 QC 标准的

2026年6月8日

首次发布 (实际的)

2026年6月10日

研究记录更新

最后更新发布 (实际的)

2026年6月10日

上次提交的符合 QC 标准的更新

2026年6月8日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • TABED 1/1735/2025
  • TYL-2026-2917 (其他赠款/资助编号:Ankara Yildirim Beyazit University BAP Department)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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