Simulated practice may sharpen midwifery skills and calm nerves

NCT ID NCT07788495

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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 Results may not be published yet.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)
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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

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Status unknown
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First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time

Summary

This trial explores whether adding simulation-based training to standard theoretical lessons helps midwifery students learn more about oxytocin induction and feel less anxious about it. Third-year midwifery students are randomly assigned to receive either theory alone or theory plus hands-on practice with a high-fidelity simulator and a standardized patient. Researchers then compare changes in knowledge scores and anxiety levels between the two groups to see if the extra simulation makes a difference.

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 training on oxytocin induction using a high-fidelity simulator and standardized patient
What this could lead to
If effective, this training approach could become a standard part of midwifery education, helping students feel more prepared and less anxious when managing oxytocin induction in real clinical settings.
What could go wrong
This is a small, single-center study in a specific student group, so results may not apply broadly. Also, improved knowledge and reduced anxiety in training may not directly translate to better 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

80 people

The number who actually took part.

Started

Nov 2024

Finished

May 2025

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

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: * Being enrolled as a third-year undergraduate student in the Department of Midwifery, Faculty of Health Sciences, Istanbul Medipol University, during the spring semester of the 2024-2025 academic year * Having successfully completed the Childbirth and Postpartum Period course * Having successfully completed the Childbirth and Postpartum Period Clinical Practice course * Having a cumulative grade point average of 2.70 or higher * Volunteering to participate in the study * Providing written and verbal informed consent Exclusion Criteria: * Not meeting one or more of the inclusion criteria * Declining to participate in the study * Not providing written or verbal informed consent

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Istanbul Medipol University, Faculty of Health Sciences

    Istanbul, Beykoz, 34810, Turkey (Türkiye)

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