Preeclamptic Pregnancy Care Education
The Effects of Simulation on Knowledge and Self-efficacy of Nurses and Midwives in Preeclamptic Pregnancy Care Education
1 other identifier
interventional
61
1 country
1
Brief Summary
The aim of this study is to evaluate the effect of simulation training in nurses and midwives on knowledge and self-efficacy regarding preeclamptic pregnancy care. It is an important step in providing safe care to patients, as a learning environment is provided in which environmental risks are minimized with simulation applications. Simulation-based trainings are environments that allow each student to learn, equitable, based on adult learning principles, and open to different learning styles. The interests and needs in these environments are defined together by the learner and the educator. By keeping the experiences of the learner at the forefront, the opportunity is given to learn by doing and supported with feedback. Preeclampsia is clinically defined as a blood pressure of 140/90 mmHg or above after the 20th week of pregnancy and the addition of proteinuria (300mg / 24 hours). It can develop in about 5-10% of all pregnancies. It is defined as a nulliparous disease since it is seen in approximately 85% of women during their first pregnancy. Preeclampsia constitutes 15% of the causes of maternal mortality in our country. In studies evaluating the effectiveness of simulation training in planning the follow-up and care of preeclampsia, it was determined that this method increases the knowledge and self-confidence of nurses. For example; Christian and Krumwiede's study they found that the self-efficacy rates were significantly higher in the post-simulation test. In his study, Olubumno investigated the importance of simulation in increasing the critical thinking of perinatology nurses in the care of preeclamptic pregnant women, he found that the pre-test and post-test scores increased by 0.75 points, and this difference between the scores is statistically significant. Tabatabaeian et al., In their study comparing the effects of simulation-based education, coeducation and theoretical education on the performance of midwives in preeclampsia and eclampsia, found that the mean of the simulation group was higher than the other two groups. Preeclampsia is an important obstetric emergency in women's health and disease nursing. Thus, when they start working in the clinic, it is aimed to be able to suspect preeclampsia with the anamnesis they received from the pregnant who applied to them, and to gain them with the simulation method what they should pay attention to and how to do in the follow-up of the pregnant woman hospitalized with the diagnosis of preeclampsia. Studies conducted in our country did not include studies involving students and healthcare professionals in the management of preeclampsia with simulation methods. Therefore, it is aimed to contribute to the literature with this study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2020
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 10, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 18, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
August 17, 2020
CompletedFirst Submitted
Initial submission to the registry
January 26, 2021
CompletedFirst Posted
Study publicly available on registry
June 7, 2021
CompletedJune 7, 2021
June 1, 2021
8 days
January 26, 2021
June 4, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The level of knowledge about preeclamptic pregnancy care is higher in the group that received training with the lecturing and high-reality simulation method compared to the group that received training only with lectures
"Self-efficacy for preeclamptic pregnancy care" scale was developed and used in the follow-up and care of preeclamptic pregnant women in order to evaluate the perception of self-efficacy towards nursing care in critical obstetric conditions related to preeclampsia in nurses and midwives. It's a 20-item instrument using a five-point scale.
Six weeks
Secondary Outcomes (2)
Educational Practices Questionnaire
One week after theoretical training
Student Satisfaction and Self-Confidence in Learning Scale
One week after theoretical training
Study Arms (2)
Simulation based education
EXPERIMENTALSimulation is a technique that creates a situation or environment that allows people to experience the representation of a real event, practice, learn, evaluate, test, or gain an understanding of systems or human actions
Traditional education
NO INTERVENTIONNecessary procedures explained theoretically
Interventions
It is an important step in providing safe care to patients, as a learning environment is provided in which environmental risks are minimized with simulation applications. Simulation-based trainings are environments that allow each student to learn, equitable, based on adult learning principles, and open to different learning styles. In these environments, interests and needs are defined together by the learner and the educator. By keeping the experiences of the learner at the forefront, the opportunity is given to learn by doing and is supported with feedback.
Eligibility Criteria
You may qualify if:
- Working for 1-5 years.
- Working in the gynecology inpatient services and delivery rooms of hospitals.
- To be a graduate nurse or midwife.
- Volunteering to participate in the study.
You may not qualify if:
- Being a high school graduate working in the related field
- Having just graduated from a related field
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medipol University Hospitals
Istanbul, 34214, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 26, 2021
First Posted
June 7, 2021
Study Start
July 10, 2020
Primary Completion
July 18, 2020
Study Completion
August 17, 2020
Last Updated
June 7, 2021
Record last verified: 2021-06
Data Sharing
- IPD Sharing
- Will not share