The Effect of Disaster Midwifery Education Program on Disaster Risk Perception and Self-Efficacy Levels of Midwifery Students
NCT ID: NCT06897423
Last Updated: 2025-03-26
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
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COMPLETED
NA
80 participants
INTERVENTIONAL
2025-03-05
2025-03-15
Brief Summary
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In this semi-experimental pre-test and post-test design and control group planned research, in order to determine the sample size; the data were normally distributed, the standard deviation of the main mass was estimated as 1 and the effect size (effect size, difference) as 0.8.
For the analysis to be conducted, it was calculated that the highest power value of the research would be 0.942182 in the case of taking two independent n₁=40, n₂=40 samples at a 5% significance level. The G-power analysis result is given below. Students who volunteer to participate in the study will be assigned to the intervention and control groups using the computer-aided simple random sampling method. Computer-aided randomization will be used in the study, and the number of cases will be entered through the program with the URL address https://www.randomizer.org and random assignment will be made to the intervention and control groups. The study will be conducted single-blind. Midwifery students will be administered the "Disaster Risk Perception" and "Self-Efficacy Scale in Disaster Intervention" before and 8 weeks after the first training. Each training period is limited to 60 minutes, once a week.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Intervention group (n:40)
Midwifery students in the intervention group of the study will receive 8 weeks of disaster midwifery training. The training content will be covered in 8 main categories: "safe prenatal, delivery and postnatal period", "women's reproductive health services", "family planning", "immunization", "violence and sexually transmitted infections" and "newborn and infant care", "reproductive health in disadvantaged groups", "emergency obstetric situations". The training content will be supported by distributing a 12-page training booklet consisting of these contents to the participants. Each training will be planned for 60 minutes.
Education
Midwifery students in the intervention group of the study will receive 8 weeks of disaster midwifery training. The training content will be covered in 8 main categories: "safe prenatal, delivery and postnatal period", "women's reproductive health services", "family planning", "immunization", "violence and sexually transmitted infections" and "newborn and infant care", "reproductive health in disadvantaged groups", "emergency obstetric situations".
Control group (n:40
no intervention After the research is completed, it is planned to give the same training to the control group.
No interventions assigned to this group
Interventions
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Education
Midwifery students in the intervention group of the study will receive 8 weeks of disaster midwifery training. The training content will be covered in 8 main categories: "safe prenatal, delivery and postnatal period", "women's reproductive health services", "family planning", "immunization", "violence and sexually transmitted infections" and "newborn and infant care", "reproductive health in disadvantaged groups", "emergency obstetric situations".
Eligibility Criteria
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Inclusion Criteria
* Health Sciences University, Hamidiye Health Sciences Faculty Midwifery Department Being an active student in the 3rd year.
Exclusion Criteria
18 Years
FEMALE
Yes
Sponsors
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Saglik Bilimleri Universitesi
OTHER
Responsible Party
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YASEMİN AYDIN KARTAL
Assoc. Prof.
Locations
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University of Health Sciences
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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SBU-AYDINKARTAL-011
Identifier Type: -
Identifier Source: org_study_id
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