Effect of Simulation Based Safety Mobilization Program on Patient Outcomes
- Conditions
- Patient OutcomesSimulation Based Learning
- Interventions
- Other: Simulation based safety mobilization program
- Registration Number
- NCT06484270
- Lead Sponsor
- Istanbul Medipol University Hospital
- Brief Summary
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)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 62
- 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
Nurses
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental group Simulation based safety mobilization program Nurses receiving simulation-based training Patients receiving care from these nurses
- Primary Outcome Measures
Name Time Method Patient outcomes-Amount of Wound Drenage (ml) 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 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 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 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 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 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.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Istanbul Medipol University
🇹🇷Istanbul, Turkey