Effect of Forward-leaning Position on Vital Signs, Pain and Anxiety of Children With Acute Asthma Attacks: A Randomized Controlled Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 86
- 试验地点
- 2
- 主要终点
- Change in Pulse Rate
研究概览
简要总结
The purpose of this study was to establish the effect on pulse rate, oxygen saturation, respiratory rate, pain and anxiety levels of Fowler's and the forward-leaning positions during nebulization in children experiencing asthma attacks.
详细描述
In the first stage, data on the children who agreed to participate in the study were recorded on the "Patient Identification Form" 10 minutes before the procedure by the researcher during a face-to-face interview. The children's body temperature, oxygen saturation, pulse rate and respiratory rate were measured. Upon explaining the FPS-R, the children were asked whether they had experienced pain before treatment, and to point at the pain level felt from among the faces on the scale. Then, CSA was explained and the children, and their level of anxiety on the scale was recorded. The pre-nebulization findings were recorded.
In the second stage, the salbutamol therapy prescribed by the physician was administered to the participating children with a nebulizer three times at 20-minute intervals. During nebulization, the study group patients were placed in forward-leaning position, placing a pillow on their knees, while the control group was placed in Fowler's position on a chair. Nebulization took an average of 10 minutes for each child. Oxygen saturation, pulse and respiratory rate were recorded immediately after the mask was removed. The children were allowed to rest for 20 minutes in Fowler's position.
In the third stage, oxygen saturation, pulse and respiratory rate were determined immediately after the mask was removed following a 10-minute second nebulization. The values determined were recorded, and the children were allowed to rest for 20 minutes in Fowler's position.
In the fourth stage, oxygen saturation, pulse and respiratory rate were determined immediately after the mask was removed following the 10-minute third nebulization. The children were asked whether they had pain, and to point at the pain level represented by the faces on the scale. The patients then marked their level of anxiety on the CSA. The post-nebulization findings were recorded.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 6 Years 至 11 Years(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •To be between 6-11 ages,
- •Having a body temperature below 37.2°C at admission,
- •Having been prescribed nebulized salbutamol by the physician during data collection,
- •Having not using bronchodilators or corticosteroid drugs within the last 6 hours,
- •Having no other respiratory system disease,
- •Verbal and written consent of the child and parent to participate in the study.
排除标准
- •Administering drugs other than nebulized salbutamol to the child during data collection,
- •Having an obstacle for positioning (Lordosis, kyphosis, scoliosis, chest wall deformities, previous surgical procedure, etc.),
- •Child and parent not knowing Turkish.
结局指标
主要结局
Change in Pulse Rate
时间窗: 90 minute
Heart rate will be monitored
Change in chest pain score
时间窗: 90 minute
Pain score will be evaluated with The faces pain scale-revised (FPS-R).
Change in Oxygen Saturation
时间窗: 90 minute
Oxygen saturation will be monitored
Change in respiratory rate
时间窗: 90 minute
Respiratory rate will be monitored
Change in anxiety score
时间窗: 90 minute
Anxiety score will be evaluated with The children state anxiety scale (CSA).
次要结局
未报告次要终点
研究者
Gamze Kas Alay
Research Assistant
Kastamonu University
