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临床试验/NCT04019236
NCT04019236Unknown不适用

Effect of Implementing Nursing Care on Breathing Discomfort and Its Outcomes Among Mechanically Ventilated Patients

Assiut University2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2018年12月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
90
试验地点
2
主要终点
Prevalence of breathing discomfort among Mechanically ventilated patients

研究概览

简要总结

Breathing discomfort (dyspnea) during mechanical ventilation in the ICU may complicate care.

详细描述

Patients on ventilators experience a variety of discomforts: symptoms (dyspnea ,fatigue , pain ) ,emotions (depression, anxiety ,panic) and feeling of lack to control .Patients may or may not express this discomfort outwardly with agitation ,restlessness ,grimacing or increase in the vital signs (heart rate ,blood pressure ,breathing frequency).The aim of the present study is to assess the prevalence of dyspnea among mechanically ventilated patients, Describe interventions that may alleviate breathing discomfort and examine its impact on clinical outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Intubated or tracheostomized patients who were mechanically ventilated for >24 hrs.
  • Age : 18-60 yrs
  • Patients with Respiratory diseases
  • Patients during spontaneous breathing trial

排除标准

  • • Patients with acidosis, anemia ,drug poisoning,psychogenic disorders or neuro-muscular disorders
  • (non invasive ventilation)NIV

研究组 & 干预措施

" interventional "

Other

New other than Routine nursing care will be used.

干预措施: visual analogue scale (VAS),Respiratory distress observational scale (RDOS) and other Nursing care (Other)

" Control group "

No Intervention

Routine care only will be done for this group

结局指标

主要结局

Prevalence of breathing discomfort among Mechanically ventilated patients

时间窗: 1year

visual analogue scale "VAS" for conscious patients and respiratory observational distress scale "RDOS" for unconscious patients

Effect of nursing intervention on patient and ICU

时间窗: 1year

Clinical outcomes "length of stay,type of discharge or other morbidities"

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Eman Mamdouh Aziz soliman

Principal Investigator

Assiut University

研究点 (2)

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