Patient Outcomes, Simulation Based Learning
Conditions
Keywords
simulation based learning, patient outcomes, safety mobilization
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)
Interventions
OTHERSimulation 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.
Sponsors
Istanbul Medipol University Hospital
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Caregiver)
Masking description
Participant: patients undergoing surgery in post-op 0 and 1 Care provider: surgical nurses
Intervention model description
An experimental and follow-up study a pre-test, post-test with control group.
Eligibility
Sex/Gender
ALL
Age
22 Years to 32 Years
Healthy volunteers
Yes
Inclusion 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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- 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-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. |
| 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-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. |
| 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. |
Countries
Turkey (Türkiye)
Outcome results
None listed