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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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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental group | Experimental | Nurses receiving simulation-based training Patients receiving care from these nurses |
|
| Control group | No Intervention | Nurses receiving theoritical education Patients receiving care from these nurses |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 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. |
| 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. |
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Nurses Inclusion Criteria:
Patient Inclusion Criteria:
Nurses Exclusion Criteria:
Patient Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Istanbul Medipol University | Istanbul | Turkey (Türkiye) |
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An experimental and follow-up study a pre-test, post-test with control group.
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Participant: patients undergoing surgery in post-op 0 and 1 Care provider: surgical nurses
|
| Before and after the patient's first mobilization during a day |