Simulation training could boost midwife skills and motivation
NCT ID NCT07543133
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether simulation-based childbirth training helps midwives improve their safe motherhood practices and stay motivated. About 132 midwives with 5 years or less experience will either receive the training or not. Researchers will measure changes using questionnaires before and after the training.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 132 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Midwives working in healthcare institutions affiliated with the provincial health directorate * Having 5 years or less professional experience * Actively involved in prenatal, intrapartum, or postpartum care * Voluntary participation with written informed consent Exclusion Criteria: * Working in administrative positions * Previously received simulation-based childbirth or advanced obstetric simulation training * Inability to attend the full training program or complete data collection
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Selçuk University
Konya, Selçuklu, 42130, Turkey (Türkiye)
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