Effect of Simulation Based Safety Mobilization Program on Patient Outcomes

Medipol Health Group

Status: Completed

Conditions: Patient Outcomes; Simulation Based Learning

Treatments: Other: Simulation based safety mobilization program

Study type: Interventional

Funder types: Other

Identifiers

NCT06484270

13579

Details and patient eligibility

About

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)

Enrollment: 62 patients

Sex: All

Ages: 22 to 32 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose: Supportive Care

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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62 participants in 2 patient groups

Experimental group

Experimental group

Description:

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

Treatment:

Other: Simulation based safety mobilization program

Control group

No Intervention group

Description:

Nurses receiving theoritical education Patients receiving care from these nurses