Supportive Care-Based Training and Psychological Outcomes in Midwifery Students (NCT07322484) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Supportive Care-Based Training and Psychological Outcomes in Midwifery Students
Turkey (Türkiye)92 participantsStarted 2025-09-15
Plain-language summary
The aim of this study is to comparatively evaluate the effects of trauma-informed supportive care model training in childbirth and universal supportive care model training in childbirth provided to midwifery students on their clinical skill self-efficacy in the delivery room, state anxiety, and secondary traumatic stress levels.
Who can participate
Age range
18 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:
* Voluntary participation in the study
* Native Turkish speakers
* Enrollment as a fourth-year student in the Midwifery Department of Mersin University during the 2025-2026 academic year
* Enrollment in Perinatal Health Practices I or Perinatal Health Practices II
* Participation in delivery room clinical practice at Mersin City Training and Research Hospital
* No diagnosed psychiatric disorder and no use of psychiatric medication
Exclusion Criteria:
* Withdrawal from the study at any stage upon the participant's own request
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
Clinical Skills Self-Efficacy
Timeframe: before the training and immediately after completion of delivery room clinical practice
2
State and Trait Anxiety
Timeframe: Trait Anxiety-before the training and one week after completion of delivery room practice; State Anxiety-immediately after completion of delivery room practice