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Simulation training boosts student skills in managing postpartum bleeding

NCT ID NCT07618442

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at whether simulation-based education helps midwifery students learn to manage postpartum hemorrhage (heavy bleeding after childbirth). Forty-five third-year students were split into two groups: both got traditional lectures, but one group also practiced with a high-fidelity birthing simulator. Researchers measured their knowledge, skills, and confidence before, right after, and four weeks later. The goal was to see if simulation training leads to better learning than lectures alone.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Simulation-based postpartum hemorrhage management education
What this could lead to
If successful, this approach could improve how midwifery students are trained to handle postpartum hemorrhage, potentially leading to better real-world outcomes for mothers.
What could go wrong
This is a small, single-center study with only 45 students, so results may not apply broadly. It measures skills in a simulation, not actual patient outcomes.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

45 people

The number who actually took part.

Started

May 2023

Finished

Jun 2023

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 25 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Third-year undergraduate midwifery students enrolled in the Department of Midwifery during the 2022-2023 academic year * Completion of the Normal Birth and Midwifery Care course * Enrollment in the High-Risk Birth and Midwifery Care course during the study period * Voluntary agreement to participate in the study * Ability to attend all study sessions and follow-up assessments Exclusion Criteria: * Previous participation in structured postpartum hemorrhage simulation-based training * Absence from any part of the educational intervention or outcome assessments * Withdrawal of consent during the study period

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Conditions

The condition(s) this trial relates to.

Postpartum Hemorrhage

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Istanbul University - Cerrahpasa

    Istanbul, 34055, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.