Midwifery Students' Opinions on Educational Material Development and Evaluation in Birth Education (NCT06989528) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Midwifery Students' Opinions on Educational Material Development and Evaluation in Birth Education
Turkey (Türkiye)25 participantsStarted 2025-05-10
Plain-language summary
This qualitative study aims to explore the experiences of midwifery students in preparing educational materials as part of the "Normal Birth and Postpartum Period" course at Antalya Bilim University. The study will evaluate both the students' perspectives on the preparation process and the educational materials they developed. The research is designed to support the development of professional skills by engaging students in the creation of tangible learning tools such as models and visual materials.
Who can participate
Age range
17 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 3rd-year midwifery students
* Enrolled in the "Normal Birth and Postpartum Period" course
* Voluntary participation and informed consent
* Completion of material preparation task
Exclusion Criteria:
* Withdrawal from the course or failure to attend data collection sessions
* Incomplete or substandard educational material submission
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Themes identified in students' responses during semi-structured interviews on the impact of educational material preparation on professional knowledge and skills
Timeframe: January 2025 (end of the course)
2
Scores assigned to educational materials prepared by students, based on expert rubric assessing scientific accuracy, usability, visual quality, and clinical applicability
Timeframe: December 2024 - January 2025 (evaluation phase)