Effect of Simulation Based Safety Mobilization Program on Patient Outcomes

The Effect of Simulation Based Safety Mobilization Program Toward Nurses on Patient Outcomes

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)

Study Overview

• Status: Completed
• Conditions: Patient Outcomes; Simulation Based Learning
• Intervention / Treatment: Other: Simulation based safety mobilization program

• Study Type: Interventional
• Enrollment (Actual): 62
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Turkey
  • Istanbul, Turkey
    • Istanbul Medipol University

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: Yes

Description

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

Nurses Exclusion Criteria:

• 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 Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Experimental group; Nurses receiving simulation-based training Patients receiving care from these nurses	Other: Simulation based safety mobilization program; Nurse participants experienced safe patient mobilization with a simulation-based learning method with a standardized patient for 4 weeks. Patient participants were mobilized safely under the supervision of a nurse and the care results were measured.
No Intervention: Control group; Nurses receiving theoritical education Patients receiving care from these nurses

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Practice performance	The performance of nurses in the intervention and control groups during the mobilization experiences was measured with a checklist.	one week during the simulation experience
Patient outcomes- Blood pressure	It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on vital sign-blood pressure.	Before and after the patient's first mobilization during a day
Patient outcomes-Amount of Wound Drenage (ml)	It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on surgical field drenage.	Before and after the patient's first mobilization during a day
Patient outcomes-Satisfaction questionnaire	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.	Before and after the patient's first mobilization during a day
Patient outcomes-Pain scale	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.	Before and after the patient's first mobilization during a day
Patient outcomes- Heart rate	It is measured to determine the effect of mobilization performed by nurses in the intervention and control groups on vital signs-heart rate.	Before and after the patient's first mobilization during a day

Collaborators and Investigators

• Sponsor: Istanbul Medipol University Hospital

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2024
• Primary Completion (Actual): June 1, 2024
• Study Completion (Actual): June 30, 2024

Study Registration Dates

• First Submitted: June 12, 2024
• First Submitted That Met QC Criteria: June 25, 2024
• First Posted (Actual): July 3, 2024

Study Record Updates

• Last Update Posted (Actual): August 12, 2024
• Last Update Submitted That Met QC Criteria: August 9, 2024
• Last Verified: August 1, 2024

More Information

Terms related to this study

• Keywords: patient outcomes; simulation based learning; safety mobilization
• Other Study ID Numbers: 13579

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No