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CompletedNCT07893990Updated Oct 26, 2026

Comparison of Three Teaching Methods for Urinary Catheterization in Nursing Students

An interventional study of Training on performing urinary catheterization using simulation in Urinary Catheterization, Urinary Catheterization Skills and Nursing Students, sponsored by Cukurova University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by Cukurova University · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Mar 2025, registered Oct 2026).
Updated Oct 26, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
112
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Research Questions

  1. Do total learning motivation and sub-dimension scores (attention-relevance, confidence-satisfaction) differ significantly among nursing students using different instructional materials for urinary catheterization training?
  2. Do students' perceptions of theoretical and skill competence differ significantly across the study groups?
  3. Do the distributions of procedural steps reported as most difficult by students differ across the groups?
02

Conditions studied

  • Urinary Catheterization
  • Urinary Catheterization Skills
  • Nursing Students
  • Learning Methodology
  • Simulation Training

Keywords

  • instructional material
  • learning motivation
  • virtual reality
  • urinary catheterization
03

In context

Lead sponsor

Cukurova University is the lead sponsor of 258 studies on the registry; 49 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Being enrolled in the Fundamentals of Nursing II course for the first time, being over the age of 18, having not previously received training related to urinary catheterization, and not being a member of any health-related profession.

Exclusion criteria

Exclusion Criteria:

  • The criteria have been established as failing to attend at least one of the theoretical or laboratory sessions and either incompletely filling out or failing to fill out the data collection forms.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
112 participants (actual)

Study arms

  • Experimental
    Low-fidelity simulator group

    Low-fidelity simulator group: Material: A low-fidelity simulator (Tellyes Urinary Model - TYE1826)-a part-task trainer consisting solely of the female external genitalia-was used. Application Characteristics: With this model, the user feels no resistance or pressure as the catheter advances through the urinary system. Internal structures such as the urethra and bladder cannot be observed from the outside, and the distance the catheter travels is significantly shorter than the actual anatomical distance. Procedure: Following a joint theoretical training session, this group performed the urinary catheterization procedure on the low-fidelity model for 10 minutes in accordance with a standard scenario, subsequently received feedback, and completed data collection forms.

    Other: Training on performing urinary catheterization using simulation

  • Experimental
    High-fidelity simulator group

    High-fidelity simulator group: Material: A computer-controlled, full-body, high-fidelity female patient simulator (Noelle S550.100, Gaumard Scientific, USA) was used. Application Features: The simulator includes a bladder reservoir, a urethra, and a valve system representing the internal urethral sphincter. This allows the user to physically feel the resistance created by these structures as the catheter advances. When the catheter reaches the bladder, a yellow artificial fluid mimicking urine flows out, and the catheter balloon can be inflated and deflated using a syringe. Additionally, the operator can use the computer to enable the simulator to provide verbal responses to the student's questions regarding pain, and vital signs can be monitored on a bedside monitor. Procedure: Following a joint theoretical training session, students completed the procedure on this full-body simulator over a 10-minute period, after which they received feedback and filled out the relevant forms.

    Other: Training on performing urinary catheterization using simulation

  • Experimental
    Virtual reality simulation group

    Virtual reality simulation group: Materials: 3D software (VR OTTO) developed by a technology company and virtual reality headsets were used. Application Features: In this software, developed based on procedural steps, students performed urinary catheterization on a patient lying in a bed within a virtual environment, using motion-sensing hand controllers that corresponded to real-world visuals. Process: Following a shared theoretical training session, students in this group completed a 10-minute practice session using the virtual reality equipment, after which they received feedback and completed questionnaires.

    Other: Training on performing urinary catheterization using simulation

Interventions

  • OtherTraining on performing urinary catheterization using simulation

    Students received training in performing urinary catheterization using one of three different types of simulation.

06

What researchers measure

Primary outcomes

  1. Total Score on the Turkish Instructional Materials Motivation Survey

    Motivation toward the assigned urinary catheterization simulation material is assessed using the 24-item Turkish version of the Instructional Materials Motivation Survey, adapted by Kutu and Sozbilir. The total score is calculated by summing the item scores and ranges from 24 to 120. Higher scores indicate greater motivation toward the instructional material. The same instrument is administered in the low-fidelity, high-fidelity, and virtual reality simulation groups.

    Time frame: immediately after completion of the assigned urinary catheterization simulation session and feedback.

Secondary outcomes

  1. Self-Reported Competence in Urinary Catheterization Skills

    Perceived skill competence is assessed using a single question in the researcher-developed Student Information Form: "Do you consider yourself competent in performing urinary catheterization?" Response options are "Yes," "No," and "Undecided." The outcome is the percentage of participants selecting each response category in each simulation group. This measure assesses perceived competence rather than objectively observed skill performance.

    Time frame: immediately after completion of the assigned urinary catheterization simulation session and feedback.

Other outcomes

  1. Self-Reported Competence in Theoretical Knowledge of Urinary Catheterization

    Perceived theoretical knowledge competence is assessed using a single question in the researcher-developed Student Information Form: "Do you consider your theoretical knowledge of urinary catheterization adequate?" Response options are "Yes," "No," and "Undecided." The outcome is the percentage of participants selecting each response category in each simulation group. This measure assesses perceived knowledge competence rather than performance on an objective knowledge test.

    Time frame: immediately after completion of the assigned urinary catheterization simulation session and feedback.

  2. Attention-Relevance Subscale Score on the Turkish Instructional Materials Motivation Survey

    Attention and perceived relevance of the assigned simulation material are assessed using the 11-item Attention-Relevance subscale of the 24-item Turkish Instructional Materials Motivation Survey. The subscale score is calculated by summing its item scores and ranges from 11 to 55. Higher scores indicate greater attention and perceived relevance. The same subscale is administered in all three simulation groups.

    Time frame: immediately after completion of the assigned urinary catheterization simulation session and feedback.

  3. Confidence-Satisfaction Subscale Score on the Turkish Instructional Materials Motivation Survey

    Confidence and satisfaction related to the assigned simulation material are assessed using the 13-item Confidence-Satisfaction subscale of the 24-item Turkish Instructional Materials Motivation Survey. The subscale score is calculated by summing its item scores and ranges from 13 to 65. Higher scores indicate greater confidence and satisfaction. The same subscale is administered in all three simulation groups.

    Time frame: immediately after completion of the assigned urinary catheterization simulation session and feedback.

  4. Self-Reported Most Difficult Step in Urinary Catheterization

    The most difficult procedural step is assessed using a single-choice question in the researcher-developed Student Information Form. Participants select one of seven categories: communicating with the patient, following the procedural steps in the correct order, maintaining aseptic technique, inserting the catheter appropriately, inflating the catheter balloon appropriately, checking catheter position, or securing the catheter correctly. The outcome is the percentage of participants selecting each category in each simulation group.

    Time frame: immediately after completion of the assigned urinary catheterization simulation session and feedback.

07

Study locations

1 site
  • Cukurova University Health Science Faculty Nursing Department
    Adana, Turkey (Türkiye)
08

References and documents

Study documents

  • Study protocol · Sep 29, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No — Consent was obtained from the participants on the condition that the data would be used anonymously solely for the purpose of the academic study. There is no permission for data sharing.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 26, 2026
Show all 1 update
  1. Oct 26, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07893990
Responsible party
ECE KURT (Assistant Professor, Cukurova University) — Principal investigator
First posted
Oct 26, 2026
Start date
Mar 18, 2025
Primary completion
Mar 19, 2025
Completion
Mar 20, 2025
Last update
Oct 26, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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