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Stress Ball and Video Distraction During Pediatric Enema (SAVE)

2026年7月11日 更新者:Manisa Celal Bayar University

Effects of Stress Ball Use and Video Distraction During Enema Administration on Fear, Anxiety, and Pain in Children in the Pediatric Emergency Department

This randomized controlled trial aims to evaluate the effects of stress ball use and video distraction during enema administration on fear, anxiety, and pain levels in children treated in the pediatric emergency department. Children aged 6-12 years will be randomly assigned to either the stress ball group or the video distraction group. Fear, anxiety, and pain will be assessed using validated measurement tools before, during, and after the procedure. The findings are expected to provide evidence for effective non-pharmacological interventions to improve children's comfort during enema administration.

研究概览

详细说明

This randomized controlled trial aims to determine the effects of stress ball use and video distraction during enema administration on fear, anxiety, and pain levels in children aged 6-12 years treated in the pediatric emergency department. A total of 72 children will be randomly assigned to either the stress ball group or the video distraction group using block randomization. Fear, anxiety, and pain will be assessed using the Child Fear Scale (CFS), the Children's Anxiety Scale-State (CAS-S), and the Wong-Baker FACES Pain Rating Scale. The findings of this study are expected to provide evidence for effective non-pharmacological interventions to improve children's comfort during enema administration. The study will be conducted at the Pediatric Emergency Department of Manisa Merkez Efendi State Hospital.

研究类型

介入性

注册 (实际的)

72

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

Children aged 6-12 years Admitted to the pediatric emergency department Scheduled for enema administration due to functional constipation or abdominal distension Able to communicate in Turkish No cognitive or neurological impairment No diagnosis of attention-deficit/hyperactivity disorder No analgesic medication use within the previous 6 hours Written informed consent provided by the parent or legal guardian and assent provided by the child

Exclusion Criteria:

Acute abdominal conditions requiring emergency surgery Diagnosis of Hirschsprung disease or inflammatory bowel disease Severe visual or hearing impairment that prevents participation Refusal of the child or parent to participate Inability to complete the study procedures

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:支持治疗
  • 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
实验性的:Stress Ball Group
Participants will use a stress ball during enema administration.
Participants will hold and squeeze an individual stress ball throughout the enema administration as a distraction technique.
实验性的:Video Distraction Group
Participants will watch an aquarium video with music during enema administration
Participants will watch a 3-minute aquarium video accompanied by Mozart music during enema administration to provide audiovisual distraction.

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
Fear Level
大体时间:Before and immediately after enema administration.
Fear level measured using the Child Fear Scale (CFS). Fear will be assessed using the Child Fear Scale (CFS). The scale ranges from 0 to 4, with higher scores indicating greater fear and a worse outcome.
Before and immediately after enema administration.
Anxiety Level
大体时间:Before and immediately after enema administration.
Anxiety level measured using the Children's Anxiety Scale-State (CAS-S). Anxiety will be assessed using the Children's Anxiety Scale-State (CAS-S). The scale ranges from 0 to 10, with higher scores indicating greater anxiety and a worse outcome.
Before and immediately after enema administration.
Pain Level
大体时间:Immediately after enema administration
Pain level measured using the Wong-Baker FACES Pain Rating Scale. Pain will be assessed using the Wong-Baker FACES Pain Rating Scale. The scale ranges from 0 to 10, with higher scores indicating greater pain intensity and a worse outcome.
Immediately after enema administration

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)

2026年2月1日

初级完成 (实际的)

2026年4月1日

研究完成 (实际的)

2026年4月30日

研究注册日期

首次提交

2026年7月6日

首先提交符合 QC 标准的

2026年7月6日

首次发布 (实际的)

2026年7月10日

研究记录更新

最后更新发布 (实际的)

2026年7月14日

上次提交的符合 QC 标准的更新

2026年7月11日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • MCBU-PED-ENEMA-2026-001
  • 20.478.486/3669 (注册表标识符:Health Sciences Ethics Board)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data (IPD) will not be shared due to privacy and confidentiality considerations.

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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