The Effect of a Riddle-Based Distraction Technique on Pain, Fear, and Anxiety During Cast Application in Children: A Randomized Study
The aim of this study is to determine the effect of a riddle-based distraction intervention, administered during cast application in children, on levels of pain, fear, and anxiety.
研究概览
详细说明
Thirty-eight volunteer children aged 6-12 presenting to the Emergency Department Green Zone Cast Room at hospital for cast application (upper or lower extremity) will be randomly divided into two groups: intervention (riddle-based distraction) and control group. Children will be assessed before and during/after the procedure. Pain related to the cast application will be assessed with the Wong-Baker Faces Pain Scale, fear with the Child Fear Scale, and anxiety levels with the State-Trait Anxiety Inventory for Children (STAIC). In addition, children's sociodemographic and clinical data will be recorded in the Information Form.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Gamze AKAY, 1
- 电话号码:05314536661
- 邮箱:gamzeakay_25@artvin.edu.tr
研究联系人备份
- 姓名:Elif Simay KOÇ, 2
- 电话号码:903488142666
- 邮箱:elifsimay.koc@kilis.edu.tr
学习地点
-
-
Central
-
Kilis、Central、土耳其(türkiye)
- 招聘中
- Kilis Prof. Dr. Alaeddin Yavaşca State Hospital
-
接触:
- Elif Simay KOÇ, 2
- 电话号码:+903488142666
- 邮箱:elifsimay.koc@kilis.edu.tr
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Being between 6 and 12 years of age
- Scheduled for cast application (upper or lower extremity)
- Conscious and able to communicate
- Able to understand and speak Turkish
- Having no auditory or cognitive impairments
- Having no prior exposure to a similar non-pharmacological distraction intervention
- Willingness of both the child and parent to participate in the study
Exclusion Criteria:
- Being under the influence of analgesic, sedative, or anxiolytic medication
- Having severe trauma or an unstable clinical condition requiring emergency intervention
- Presence of developmental delay, neurological disease, or conditions affecting communication
- Inability to participate in riddles due to hearing or visual impairment
- Having prior cast experience on the same extremity
- Inability to cooperate during the research process
学习计划
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:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
无干预:Control Group
Routine clinical care will be applied to the control group. No action will be taken. |
|
|
实验性的:Experimental Group
Before and during the cast application, the child will be asked age-appropriate simple riddles, encouraged to actively participate through clues, and their attention will be distracted from the procedure. |
Children who come to the hospital's cast room and meet the research criteria will be randomly assigned to the intervention group. The baseline scales and information forms will be filled out by the researcher through interviews with the child and parent before the cast application. Before the research, a pool of short, clear, and age-appropriate riddles will be prepared in consultation with experts, taking into account the cognitive levels of children aged 6-12. Prior to the procedure, brief communication will be established with the child to introduce the riddle game. During the cast preparation (preparing materials and positioning the extremity) and throughout the entire cast application process (wrapping, shaping, and setting the cast), the researcher will continuously ask the child riddles. The child's active participation will be encouraged by providing hints when needed and offering positive feedback. Active distraction turns the frightening cast room into an engaging space. |
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 |
|---|---|---|
|
Patient Identification Form
大体时间:Baseline
|
It is a form consisting of 4 questions in total, including the child's age, gender, previous fracture experience, and if any, how many times the child has experienced a fracture. It was prepared by the researcher in accordance with the literature. |
Baseline
|
|
Wong-Baker FACES Pain Rating Scale
大体时间:Baseline and up to 4 weeks
|
This scale was developed by Donna Wong and Connie Moran Baker in 1981 to assess pain levels in children. Suitable for children aged 3-18 years, the scale consists of 6 facial expressions scored from '0' to '10'. A score of "0" indicates no pain, while a score of "10" represents the worst possible pain. In our study, the child will be shown the facial expressions on the scale, asked to choose the face that best describes their pain, and the corresponding score will be recorded. |
Baseline and up to 4 weeks
|
|
Child Fear Scale - CFS
大体时间:Baseline and up to 4 weeks
|
Developed by McMurtry and colleagues, the Turkish validity of this scale was conducted by Gerçeker and colleagues. The changes in the facial muscles of a frightened expression were drawn by a graphic artist from a photograph of a frightened face. The scale features facial expressions scored from 0 to 4, where "0" indicates a neutral expression (no fear), "1" indicates a very low level of fear, "2" indicates a little fear, "3" indicates a greater level of fear, and "4" indicates the highest level of fear. In our study, the child will be shown the facial expressions on the fear scale, asked to select how they feel, and the corresponding score will be recorded. |
Baseline and up to 4 weeks
|
|
State-Trait Anxiety Inventory for Children - STAIC / Thermometer
大体时间:Baseline and up to 4 weeks
|
Developed to measure anxiety in children, the Turkish validity of this tool was confirmed by Gerçeker and colleagues (Ayar et al.). The scale utilizes a thermometer visual with a bulb at the bottom representing a score of "0" and lines extending upwards divided into 10 sections reaching a score of "10". The child is explained that as their finger moves up from the bulb, their anxiety increases, whereas the bulb represents playing happily with friends. In our study, the child will be asked to point to the thermometer according to how they feel during the procedure, and the corresponding score will be recorded. |
Baseline and up to 4 weeks
|
合作者和调查者
调查人员
- 首席研究员:Gamze AKAY, 1、Artvin Coruh University
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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.