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Completed

NCT Number: NCT06484270

Effect of Simulation Based Safety Mobilization Program 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)

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Key information

Conditions

Patient Outcomes Simulation Based Learning

Age range

22 year–32 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Istanbul Medipol University

Istanbul, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

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.

Primary outcomes

  1. Practice performance

    Time frame: 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.

  2. Patient outcomes- Blood pressure

    Time frame: 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.

  3. Patient outcomes-Amount of Wound Drenage (ml)

    Time frame: 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.

  4. Patient outcomes-Satisfaction questionnaire

    Time frame: 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.

  5. Patient outcomes-Pain scale

    Time frame: 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.

  6. Patient outcomes- Heart rate

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

Istanbul Medipol University Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jul 3, 2024
Registry last updated
Aug 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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