Effect of Simulation Based Safety Mobilization Program on Patient Outcomes

NCT06484270 | Completed

• 1 other identifier: 13579
• Study Type: interventional
• Target: 62
• Locations: 1 country
• Sites: 1

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)

Conditions

Patient Outcomes; Simulation Based Learning

Keywords

simulation based learning; patient outcomes; safety mobilization

Outcome Measures

Primary Outcomes (6)

• 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

Study Arms (2)

Experimental group

EXPERIMENTAL

Nurses receiving simulation-based training Patients receiving care from these nurses

Other: Simulation based safety mobilization program

Control group

NO INTERVENTION

Nurses receiving theoritical education Patients receiving care from these nurses

Interventions

Simulation based safety mobilization program OTHER

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.

Experimental group

Eligibility Criteria

• Age: 22 Years - 32 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• 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.
• Agreeing to participate in the study,
• Not having a mental or cognitive disease
• Having undergone major surgery

You may not qualify if:

• Be a simulation-based learning experience
• Have less than 3 months of professional experience
• Having undergone minor surgery
• Having a mental or cognitive disease

Sponsors & Collaborators

• Istanbul Medipol University Hospital: lead

Study Sites (1)

Istanbul Medipol University

Istanbul, Turkey (Türkiye)

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, CARE PROVIDER
• Masking Details: Participant: patients undergoing surgery in post-op 0 and 1 Care provider: surgical nurses
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Asst.Prof.

Model Details: An experimental and follow-up study a pre-test, post-test with control group.

Study Record Dates

• First Submitted: June 12, 2024
• First Posted: July 3, 2024
• Study Start: January 1, 2024
• Primary Completion: June 1, 2024
• Study Completion: June 30, 2024
• Last Updated: August 12, 2024

Record last verified: 2024-08

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)