Disaster Midwifery TrainingNCT06897423
The Effect of Disaster Midwifery Education Program on Disaster Risk Perception and Self-Efficacy Levels of Midwifery Students
A study testing Education in people with Disaster Midwifery Training, run by Saglik Bilimleri Universitesi at 1 site in Turkey (Türkiye).
Trial summary
This research was planned to examine the effect of disaster midwifery education on the disaster risk perception and self-efficacy levels of midwifery students. The research universe will consist of third-year students studying at the Department of Midwifery, Hamidiye Faculty of Health Sciences (HSBF), Health Sciences… Read more about this study
- Who is it for?
- Ages 18 years and older, women onlyHealthy volunteers can take part
- Conditions the study is for
- Disaster Midwifery Training
- What is being tested?
- Education
- Type of treatment
- Vaccines
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 5 Mar 2025to 15 Mar 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Volunteer to participate in the research.
- Health Sciences University, Hamidiye Health Sciences Faculty Midwifery Department Being an active student in the 3rd year.
Who cannot join
- Being a passive student in the 3rd year of the Department of Midwifery, Hamidiye Faculty of Health Sciences, University of Health Sciences.
Trial locations and contacts
1 site in 1 country.
About this study
This research was planned to examine the effect of disaster midwifery education on the disaster risk perception and self-efficacy levels of midwifery students. The research universe will consist of third-year students studying at the Department of Midwifery, Hamidiye Faculty of Health Sciences (HSBF), Health Sciences University (SBU) in the spring semester of the 2023-2024 academic year (N: 80).
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.
- Conditions
- Disaster Midwifery Training
- Being tested
- Education
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
EducationOther
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".
| Study group | Role | What they receive |
|---|---|---|
| Intervention group (n:40) | Experimental | 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. Receives: Other: Education |
| Control group (n:40 | No intervention | no intervention After the research is completed, it is planned to give the same training to the control group. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Introductory Information Form:
This form, created by researchers based on literature, includes questions about the participants' age, high school graduation, whether they see themselves as sufficient against disasters, etc.
Measured: 10 minutes
Disaster Risk Perception Scale
The scale consists of 21 items and 4 dimensions. The scale has four sub-dimensions: "threat", "fatalism", "controllability" and "anxiety". The "threat" sub-dimension of the scale consists of seven items, the "fatalism" sub-dimension consists of three items, the "controllability" sub-dimension consists of six items and the "anxiety" sub-dimension consists of five items. The items in the scale are in a 5-point Likert format as "1- Strongly Disagree", "2- Disagree", "3-Partially Agree", "4-Agree", "5-Strongly Agree". The lowest score that can be obtained from the scale is 21 and the highest is 105. As the score obtained from the scale increases, the level of disaster risk perception increases.
Measured: 10 minutes
Self-Efficacy Scale in Disaster Response
The Disaster Response Self-Efficacy Scale, developed by Hong-Yan Li and colleagues in 2017 and Turkish validity security studies conducted by Koca and colleagues in 2018, consists of 19 items and 3 sub-dimensions, and the answers are taken with a 5-point Likert scale. A high score from the scale indicates a high level of disaster response self-efficacy. The scale has three sub-factors. Sub-factors: "On-Site Rescue Competence (Items 1 - 11)", "Disaster Psychological Nurse Competence (Items 12 - 15)" and "The nature of the role undertaken in the disaster and adaptation competence (Items 16 - 19)". The Cronbach alpha coefficient for the entire scale is 0.96. The Cronbach alpha values taken for the sub-dimensions are; on-site rescue competence was determined as 0.93, disaster psychological nurse competence was determined as 0.93, the quality of the role undertaken in the disaster and adaptation competence was determined as 0.93
Measured: 10 minutes
Secondary outcomes (3)
Introductory Information Form:
This form, created by researchers based on literature, includes questions about the participants' age, high school graduation, whether they see themselves as sufficient against disasters, etc.
Measured: 10 minutes
Disaster Risk Perception Scale
The scale consists of 21 items and 4 dimensions. The scale has four sub-dimensions: "threat", "fatalism", "controllability" and "anxiety". The "threat" sub-dimension of the scale consists of seven items, the "fatalism" sub-dimension consists of three items, the "controllability" sub-dimension consists of six items and the "anxiety" sub-dimension consists of five items. The items in the scale are in a 5-point Likert format as "1- Strongly Disagree", "2- Disagree", "3-Partially Agree", "4-Agree", "5-Strongly Agree". The lowest score that can be obtained from the scale is 21 and the highest is 105. As the score obtained from the scale increases, the level of disaster risk perception increases.
Measured: 10 minutes
Self-Efficacy Scale in Disaster Response
The Disaster Response Self-Efficacy Scale, developed by Hong-Yan Li and colleagues in 2017 and Turkish validity security studies conducted by Koca and colleagues in 2018, consists of 19 items and 3 sub-dimensions, and the answers are taken with a 5-point Likert scale. A high score from the scale indicates a high level of disaster response self-efficacy. The scale has three sub-factors. Sub-factors: "On-Site Rescue Competence (Items 1 - 11)", "Disaster Psychological Nurse Competence (Items 12 - 15)" and "The nature of the role undertaken in the disaster and adaptation competence (Items 16 - 19)". The Cronbach alpha coefficient for the entire scale is 0.96. The Cronbach alpha values taken for the sub-dimensions are; on-site rescue competence was determined as 0.93, disaster psychological nurse competence was determined as 0.93, the quality of the role undertaken in the disaster and adaptation competence was determined as 0.93
Measured: 10 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Mar 2025
- Study start5 Mar 2025
- Primary completion5 Mar 2025
- Study completion15 Mar 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Disaster Midwifery TrainingStudies of the same condition, open and under way.
- More trials run by Saglik Bilimleri UniversitesiThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 80 participants (actual)
Sponsor and investigators
- Lead sponsor
- Saglik Bilimleri Universitesi
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, YASEMİN AYDIN KARTAL, Saglik Bilimleri Universitesi
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06897423
- Sponsor's protocol ID
- SBU-AYDINKARTAL-011
- Status last verified
- Dec 2024
- First submitted
- 7 Dec 2024
- Last updated
- 26 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Disaster Midwifery Education Program on Disaster Risk Perception and Self-Efficacy Levels of Midwifery Students
- ClinicalTrials.gov ID
- NCT06897423
- Acronym / sponsor ID
- SBU-AYDINKARTAL-011
- Conditions
- Disaster Midwifery Training
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 80 participants (actual)
- Lead sponsor
- Saglik Bilimleri UniversitesiUniversity, hospital or other
- Study start
- 5 Mar 2025 (actual)
- Primary completion
- 5 Mar 2025 (actual)
- Study completion
- 15 Mar 2025 (actual)
- First posted
- 26 Mar 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This research was planned to examine the effect of disaster midwifery education on the disaster risk perception and self-efficacy levels of midwifery students. The research universe will consist of third-year students studying at the Department of Midwifery, Hamidiye Faculty of Health Sciences (HSBF), Health Sciences University (SBU) in the spring semester of the 2023-2024 academic year (N: 80).
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.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention group (n:40) | Experimental | Other: EducationMidwifery 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. |
| Control group (n:40 | No intervention | –no intervention After the research is completed, it is planned to give the same training to the control group. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Volunteer to participate in the research.
- Health Sciences University, Hamidiye Health Sciences Faculty Midwifery Department Being an active student in the 3rd year.
Key exclusion criteria (1 listed)
- Being a passive student in the 3rd year of the Department of Midwifery, Hamidiye Faculty of Health Sciences, University of Health Sciences.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| EducationMidwifery 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". | Other | Intervention group (n:40) |
Primary outcome
Introductory Information Form:
Time frame: 10 minutes
This form, created by researchers based on literature, includes questions about the participants' age, high school graduation, whether they see themselves as sufficient against disasters, etc.
Disaster Risk Perception Scale
Time frame: 10 minutes
The scale consists of 21 items and 4 dimensions. The scale has four sub-dimensions: "threat", "fatalism", "controllability" and "anxiety". The "threat" sub-dimension of the scale consists of seven items, the "fatalism" sub-dimension consists of three items, the "controllability" sub-dimension consists of six items and the "anxiety" sub-dimension consists of five items. The items in the scale are in a 5-point Likert format as "1- Strongly Disagree", "2- Disagree", "3-Partially Agree", "4-Agree", "5-Strongly Agree". The lowest score that can be obtained from the scale is 21 and the highest is 105. As the score obtained from the scale increases, the level of disaster risk perception increases.
Self-Efficacy Scale in Disaster Response
Time frame: 10 minutes
The Disaster Response Self-Efficacy Scale, developed by Hong-Yan Li and colleagues in 2017 and Turkish validity security studies conducted by Koca and colleagues in 2018, consists of 19 items and 3 sub-dimensions, and the answers are taken with a 5-point Likert scale. A high score from the scale indicates a high level of disaster response self-efficacy. The scale has three sub-factors. Sub-factors: "On-Site Rescue Competence (Items 1 - 11)", "Disaster Psychological Nurse Competence (Items 12 - 15)" and "The nature of the role undertaken in the disaster and adaptation competence (Items 16 - 19)". The Cronbach alpha coefficient for the entire scale is 0.96. The Cronbach alpha values taken for the sub-dimensions are; on-site rescue competence was determined as 0.93, disaster psychological nurse competence was determined as 0.93, the quality of the role undertaken in the disaster and adaptation competence was determined as 0.93
3 secondary outcomes
Introductory Information Form:
Time frame: 10 minutes
Disaster Risk Perception Scale
Time frame: 10 minutes
Self-Efficacy Scale in Disaster Response
Time frame: 10 minutes
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Mar 2025.
- Individual participant dataSharing planned: No
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Education in people with Disaster Midwifery Training, run by Saglik Bilimleri Universitesi at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Introductory Information Form: (time frame: 10 minutes). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Mar 2025.