Web-Based Gamification in Postpartum Hemorrhage Management Education Among Midwifery Students (NCT07688122) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Web-Based Gamification in Postpartum Hemorrhage Management Education Among Midwifery Students
128 participantsStarted 2026-10-01
Plain-language summary
This study was designed to compare the effects of web-based gamification and online classical teaching methods on knowledge level, motivation toward instructional materials, clinical self-efficacy, and satisfaction in midwifery students receiving postpartum hemorrhage management education.
Who can participate
Age range
18 Years – 40 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:
* Living in Turkey
* Aged between 18-40 years
* Female
* Native speaker of Turkish
* Fourth-year undergraduate midwifery student
* Having received basic education on postpartum hemorrhage within the curriculum
* Having access to internet and digital devices (computer, tablet, or smartphone)
* Voluntarily agreeing to participate in the study
Exclusion Criteria:
* Not attending at least 80% of the training sessions
* Not completing the data collection tools fully
* Participating in another study or training related to postpartum hemorrhage management during the research period
* Not accessing or completing the gamification modules (for the experimental group)
* Withdrawing from the study at any stage
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
Level of Motivation Towards Instructional Material
Timeframe: 24 hours after completion of the intervention
2
Postpartum Hemorrhage Management Knowledge Level
Timeframe: 24 hours before the intervention and within 24 hours after completion of the intervention
3
Clinical Skills Self-Efficacy Level
Timeframe: 24 hours before the intervention and within 24 hours after completion of the intervention
4
Satisfaction Level
Timeframe: 24 hours after completion of the intervention