Microteaching Method on Urinary Catheterization Practice Skill

April 9, 2026 updated by: Hakime Aslan, Inonu University

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

Completed

Conditions

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

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

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

Yes

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

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: 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

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

February 15, 2025

Primary Completion (Actual)

May 15, 2025

Study Completion (Actual)

September 15, 2025

Study Registration Dates

First Submitted

April 4, 2026

First Submitted That Met QC Criteria

April 9, 2026

First Posted (Actual)

April 14, 2026

Study Record Updates

Last Update Posted (Actual)

April 14, 2026

Last Update Submitted That Met QC Criteria

April 9, 2026

Last Verified

April 1, 2026

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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