Effect of Simulation Based Safety Mobilization Program on Patient Outcomes
NCT ID: NCT06484270
Last Updated: 2024-08-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
62 participants
INTERVENTIONAL
2024-01-01
2024-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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)
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Hybrid Simulation Method on Advanced Life Support Application of Nursing Students
NCT06425965
Effectiveness Of Different Simulation Methods As A Training Strategy In Basic Life Support
NCT04746898
Simulation Psychosocial Care Skills and Oncology Nursing
NCT07087470
The Effect of Simulation to Improve of Nurse's Attitudes Towards Elderly Patient
NCT05485389
Communication Skills and Anger Management Training for Nurses
NCT06827067
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experimental group
Nurses receiving simulation-based training Patients receiving care from these nurses
Simulation 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.
Control group
Nurses receiving theoritical education Patients receiving care from these nurses
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Simulation 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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
Exclusion Criteria
* Have less than 3 months of professional experience
* Having undergone minor surgery
* Having a mental or cognitive disease
22 Years
32 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Istanbul Medipol University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
pınar dogan
Asst.Prof.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Istanbul Medipol University
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
13579
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.