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Enrolling by Invitation

NCT Number: NCT07543133

Simulation-Based Childbirth Training and Midwives' Outcomes

This randomized controlled study aims to evaluate the effect of simulation-based childbirth management training on safe motherhood practices and intrinsic motivation among midwives. Participants will be randomly assigned to either an intervention group receiving simulation-based training or a control group receiving no additional training. Outcomes will be assessed using validated scales before and after the intervention.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Selçuk University

Konya, Selçuklu, 42130, Turkey (Türkiye)

About this study

Simulation-based training is an effective educational approach that allows healthcare professionals to develop clinical skills in a safe and controlled environment. This study aims to evaluate the effectiveness of simulation-based childbirth management training on safe motherhood practices and intrinsic motivation among midwives.

The study is designed as a randomized controlled trial with a pre-test and post-test design. A total of 132 midwives will be included and randomly assigned to intervention and control groups. The intervention group will receive a structured simulation-based training program over five days, including obstetric scenarios such as normal delivery, postpartum hemorrhage, shoulder dystocia, and other obstetric emergencies. Each session will include pre-briefing, simulation practice, and debriefing.

The control group will continue routine practices without any additional intervention. Data will be collected using a Personal Information Form, Safe Motherhood Scale (for healthcare professionals), and Intrinsic Motivation Scale. Outcomes will be measured before and after the intervention.

The study aims to contribute to evidence-based midwifery education by evaluating both clinical practice outcomes and motivational factors.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Simulation-Based Childbirth Management Training

Behavioral

Participants will receive simulation-based childbirth management training for five consecutive days (8 hours per day), including structured obstetric scenarios and debriefing sessions.

Primary outcomes

  1. Safe Motherhood Practices Level

    Time frame: Before training and immediately after training (Day 5)

    Measured using the Safe MotherhoodScale for Healthcare Professionals before and after the intervention. Assessed using the Safe Motherhood Scale for Healthcare Professionals, a 22-item Likert-type scale evaluating practices related to maternal and newborn safety. Higher scores indicate better safe motherhood practices.Possible score range: 22-110.

  2. Intrinsic Motivation Level

    Time frame: Before training and immediately after training (Day 5)

    Measured using the Intrinsic Motivation Scale before and after the intervention.Assessed using the Intrinsic Motivation Scale, a 21-item Likert-type scale measuring employees' intrinsic motivation across multiple dimensions. Higher scores indicate higher intrinsic motivation. Possible score range: 22-110.

Sponsors and collaborators

Lead sponsor

Selcuk University

Other

Registry information

Official study title

The Effect of Simulation-Based Childbirth Management Training on Safe Motherhood Practices and Intrinsic Motivation Among Midwives: A Randomized Controlled Study

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 21, 2026
Registry last updated
Apr 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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