- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06832319
IMPACT of KNOWLEDGE and SKILLS in MANAGEMENT of BLEEDING DURING PREGNANCY
February 12, 2025 updated by: Mine Gokduman Keles, Burdur Mehmet Akif Ersoy University
EFFECT of PERSONALIZED FEEDBACK USED in SIMULATION TECHNIQUE on KNOWLEDGE and SKILLS in MANAGEMENT of BLEEDING DURING PREGNANCY
Simulation training motivates participants to interact and collaborate, and studies on interdisciplinary groups show that it improves soft skills such as communication and teamwork.
Midwifery students' skills are the ability to apply knowledge and use their knowledge to perform tasks and solve problems.
They are cognitive in nature and include logical, intuitive and creative thinking.
Practical experiences such as the application of skills and methods, materials, tools and equipment further develop these skills.
Skills represent the application of learned abilities and the result of practical experience that emerges both cognitively and practically.
In addition, feedback is included in the methods used as an important part of clinical education
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Volunteer to participate in the research, Continuing their sophomore year in the 2024-2025 Spring semester,
Exclusion Criteria:
- Students who do not participate in theoretical explanation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
|
|
|
Active Comparator: INTERVENTION 1
|
Students in the study group will be asked to intervene in a simulated situation in the management of bleeding during pregnancy.
It will be filmed with a camera so that students can see their own mistakes after the simulated scenario.
After the scenarios are completed by the students in the control group, the mistakes in the clinical situations will be analyzed by the researchers and students in the form of questions and answers and the necessary feedback will be given to them.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Scale for Evaluating Simulation-Based Learning
Time Frame: 1 HOUR
|
1 HOUR
|
|
Student Satisfaction and Self-Confidence Scale in Learning
Time Frame: 1 HOUR
|
1 HOUR
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
February 20, 2025
Primary Completion (Estimated)
March 30, 2025
Study Completion (Estimated)
March 30, 2025
Study Registration Dates
First Submitted
February 12, 2025
First Submitted That Met QC Criteria
February 12, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 12, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Burdur_Mehmet Akif Ersoy Uni
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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