The Effect of Simulation Based Safety Mobilization Program Toward Nurses on Patient Outcomes
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 62
- 试验地点
- 2
- 主要终点
- Patient outcomes-Amount of Wound Drenage (ml)
研究概览
简要总结
The aim of the study was to evaluate the effect of safe mobilization training given to nurses through simulation-based learning method on patient care results.. The main questions it aims to answer are:
Is the safe mobilization training given to nurses by simulation-based learning method effective on the performance of nurses? Is the safe mobilization training given to nurses through simulation-based learning effective on patient outcomes?
Researchers will compare drug ABC to a placebo (a look-alike substance that contains no drug) to see if drug ABC works to treat severe asthma.
Nurse Participants will:
Experimental group: Take simulation based safety mobilization program for 4 weeks Control group: Theoretical education for 1 week (two hours)
Patient Participans will:
He/she mobilized by experimental/control groups nurse and care outcomes are measured for 1 week (once before and after practice)
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Double (Participant, Care Provider)
盲法说明
Participant: patients undergoing surgery in post-op 0 and 1 Care provider: surgical nurses
入排标准
- 年龄范围
- 22 Years 至 32 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Nurses Inclusion Criteria:
- •Agreeing to participate in the study,
- •Having no simulation-based learning experience before the study,
- •Being a bachelor's degree,
- •Being actively working in the data collection process.
- •Working in the Surgery Clinic for at least 3 months.
- •Patient Inclusion Criteria:
- •Agreeing to participate in the study,
- •Not having a mental or cognitive disease
- •Having undergone major surgery
排除标准
- •Be a simulation-based learning experience
- •Have less than 3 months of professional experience
- •Patient Exclusion Criteria:
- •Having undergone minor surgery
- •Having a mental or cognitive disease
结局指标
主要结局
Patient outcomes-Amount of Wound Drenage (ml)
时间窗: Before and after the patient's first mobilization during a day
It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on surgical field drenage.
Practice performance
时间窗: one week during the simulation experience
The performance of nurses in the intervention and control groups during the mobilization experiences was measured with a checklist.
Patient outcomes- Heart rate
时间窗: Before and after the patient's first mobilization during a day
It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on vital signs-heart rate.
Patient outcomes-Satisfaction questionnaire
时间窗: Before and after the patient's first mobilization during a day
It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on satisfaction. This questionaire was evaluated by the patient between 1 and 10 points. 1 being the lowest and 10 being the highest.
Patient outcomes- Blood pressure
时间窗: Before and after the patient's first mobilization during a day
It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on vital sign-blood pressure.
Patient outcomes-Pain scale
时间窗: Before and after the patient's first mobilization during a day
It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on pain. This measurement was made with a visual analog scale.This scale was evaluated by the patient between 1 and 10 points. 1 being the lowest and 10 being the highest.
次要结局
未报告次要终点
研究者
pınar dogan
Asst.Prof.
Istanbul Medipol University Hospital