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临床试验/NCT01559610
NCT01559610已完成不适用

Preoperatively Orientation in Cardiac Surgery: Nurses Intervention on Patients Recovery

Instituto de Cardiologia do Rio Grande do Sul2 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2008年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
180
试验地点
2
主要终点
knowledge

研究概览

简要总结

The purpose of this study is to determine whether the guidelines preoperative performed by a nurse contribute to the recovery of the patient submitted to cardiac surgery compared with the guidelines for routine.

详细描述

This is a randomized clinical trial, which included patients submitted to cardiac surgery on both sexes. They are divided in two groups: control group and intervention group.

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
Single (Participant)

入排标准

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

入选标准

  • Primary Elective Cardiac Surgical Procedures
  • Age above 18 years old
  • At least 24 hours of hospitalization before the procedure

排除标准

  • Patients who do not accept and do not signed a consenting term

研究组 & 干预措施

Control Group

No Intervention

Received preoperative guidance by a member of healthcare team with the aid of checklist

干预措施: Intervention Group (Other)

Group intervention

Other

preoperative guideline by a nurse

干预措施: Intervention Group (Other)

结局指标

主要结局

knowledge

时间窗: seven days

three questions applied on the second day of recovery at the nursery room, after the intensive care unit discharge,about type of anesthesia,endotracheal tube function and time of healing of the sternum bone.The questions had only one correct alternative.Since the randomization until the questionnaire,the study follow up took seven days.For the analysis,answers of the questionnaire were separated and the number of answers for each,and divided into the two groups.The results were presented in graphic and tables.

次要结局

  • satisfaction(seven days)

研究者

发起方
Instituto de Cardiologia do Rio Grande do Sul
申办方类型
Other
责任方
Sponsor

研究点 (2)

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