- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07527507
Microteaching Method on Urinary Catheterization Practice Skill
The Effect of the Microteaching Method on Urinary Catheterization Practice Skills and Level of Satisfaction: Randomised Controlled Trial
Aim: This study was conducted to evaluate the impact of the microteaching approach on the urinary catheterization skills and satisfaction levels of nursing students.
Desing: The study was conducted using a randomised controlled trial design. Methods: The study was conducted between February and May 2025 in the Department of Nursing at a university in eastern Türkiye. A power analysis determined that the sample size should be 60 students (30 in the experimental group and 30 in the control group). Data were collected using the "Student Information Form", the "Urinary Catheterisation Skill Assessment Checklist" and the "Visual Analog Scale-Satisfaction".
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
During the first two weeks of the study, students in both the experimental and control groups received four hours of theoretical and practical training in urinary catheterization each week. In the third week, pre-test data was collected from both the experimental and control groups. As part of this process, students were given the 'Student Information Form', the 'Urinary Catheterisation Skill Assessment Checklist' and the 'Visual Analog Scale-Satisfaction', and asked to complete them. To assess the students' skill levels in the groups, a researcher and an independent observer evaluated each student's urinary catheterisation skills individually using an unobserver-participation observation method. The results of the evaluation were recorded on checklists.
From the fourth week onwards, the experimental group underwent training using the microteaching method. The skill of performing urinary catheterization was taught over the course of six weeks using this method.
Meanwhile, the students in the control group continued their education using traditional teaching methods for five weeks.
Post-test data were collected from students in the experimental and control groups in Week 10.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Malatya
-
Malatya, Malatya, Turkey (Türkiye), 44280
- Hakime Aslan
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- To be taking Principles of Nursing II for the first time.
- To consent to the evaluation of your clinical practice and to its video recording.
- To volunteer to participate in the study.
Exclusion Criteria:
- Have completed training in urinary system procedures, in addition to basic nursing education.
- Have graduated from a vocational high school or an associate degree programme in a health-related field.
- Be willing to leave the research process.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
Control
|
|
|
Experimental: Intervention
Microteaching education
|
During the first two weeks of the study, students in both the experimental and control groups received four hours of theoretical and practical training in urinary catheterization each week. Each student was given the opportunity to perform the procedure at least once, and those who performed it inadequately or incompletely were allowed to repeat it. In the third week, pre-test data was collected from both the experimental and control groups. As part of this process, students were given the 'Student Information Form', the 'Urinary Catheterisation Skill Assessment Checklist' and the 'Visual Analog Scale-Satisfaction', and asked to complete them. From the fourth week onwards, the experimental group underwent training using the microteaching method. The skill of performing urinary catheterization was taught over the course of six weeks using this method. Post-test data were collected from students in the experimental and control groups in Week 10. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of Urinary Catheterization Skill
Time Frame: 10 week
|
During the first two weeks of the study, students in both the experimental and control groups received four hours of theoretical and practical training in urinary catheterisation each week. In the third week, pre-test data was collected from both the experimental and control groups. As part of this process, students were given the 'Student Information Form', the 'Urinary Catheterisation Skill Assessment Checklist' To assess the students' skill levels in the groups, a researcher and an independent observer evaluated each student's urinary catheterisation skills individually using an unobserver-participation observation method. The results of the evaluation were recorded on checklists. Post-test data were collected from students in the experimental and control groups in Week 10. |
10 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of satisfiction
Time Frame: 10 weeks
|
During the first two weeks of the study, students in both the experimental and control groups received four hours of theoretical and practical training in urinary catheterisation each week. In the third week, pre-test data was collected from both the experimental and control groups. As part of this process, students were given the 'Student Information Form', the ''VAS Satisfaction Scale'' to assess the students' satisfaction with teaching method levels in the groups. Post-test data were collected from students in the experimental and control groups in Week 10. |
10 weeks
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hakime Aslann
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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