ClinicalTrials.gg
CompletedNCT07824362Updated Oct 1, 2026

Video-Assisted Training for Urinary Catheterization in Nursing Students

An interventional study of Video-Assisted Training and Traditional Training in Urinary Catheterization Skills, sponsored by Behire SANÇAR. Completed at 1 site in Turkey (Türkiye). Per ClinicalTrials.gov, last updated 2026-10-01.

Primary conditionAnxiety Disorders(the registry's first term)UnverifiedIs this wrong?The registry often attaches Anxiety Disorders to studies about something else, and this study's title and listed conditions do not name it. No better condition is named, so the registry's term is kept.

Sponsored by Behire SANÇAR · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 5 months after the study started (first participant enrolled Apr 2025, registered Sep 2026).

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Phase
Not applicable
Study type
Interventional
Enrollment
74
Allocation
Randomized
Sex
All
01

Study summary

This randomized controlled study evaluated the effect of video-assisted training on urinary catheter insertion skills, state anxiety, and satisfaction with educational methods among first-year nursing students. A total of 74 students were randomly assigned to either the video-assisted training group or the control group. All participants received traditional theoretical instruction and laboratory demonstration on urinary catheter insertion. In addition, students in the intervention group watched a researcher-prepared instructional video on the procedure, while students in the control group received traditional training only. Outcomes included urinary catheter insertion skills, state anxiety, and satisfaction with educational methods.

02

Conditions studied

  • Urinary Catheterization Skills

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Keywords

  • Urinary Catheterization
  • Nursing Students
  • Video-Assisted Training
  • Nursing Education
  • State Anxiety
  • Student Satisfaction
03

In context

Anxiety Disorders Unverified

7,207 studies on the registry are indexed under Anxiety Disorders; 1,682 are open to participants now.

This study's enrollment of 74 is close to the median of 80 across 6,062 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

This is the only study on the registry with Behire SANÇAR as lead sponsor.

Compared within Anxiety Disorders, the registry's first condition term, which may not be this study's main condition. Counted across the registry records on this site, refreshed daily. How we classify →

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
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 a first-year nursing student.
  • Being enrolled in the Fundamentals of Nursing course.
  • Volunteering to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Having previously completed the Fundamentals of Nursing course.
  • Irregular attendance during the study period.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
74 participants (actual)

Study arms

  • Experimental
    Video-Assisted Training Group

    Participants received traditional theoretical instruction and laboratory demonstration on urinary catheter insertion without access to the instructional video during the study. The video was made available to the control group after completion of the study.

    Other: Video-Assisted Training · Other: Traditional Training

  • Active comparator
    Control Group

    Participants received traditional theoretical instruction and laboratory demonstration on urinary catheter insertion without access to the instructional video during the study. The video was made available to the control group after completion of the study.

    Other: Traditional Training

Interventions

  • OtherVideo-Assisted Training

    A researcher-prepared approximately 12-minute instructional video demonstrating urinary catheter insertion was provided to the intervention group through the university's learning management system (ALMS). Students could watch the video and rewatch it as needed. The video-assisted training was provided in addition to the traditional theoretical instruction and laboratory demonstration received by all participants.

  • OtherTraditional Training

    Traditional theoretical instruction and laboratory demonstration on urinary catheter insertion were provided to participants.

06

What researchers measure

Primary outcomes

  1. Urinary Catheterization Skill Performance

    Urinary catheterization skill performance was assessed using the Urinary Catheterization Skill Checklist. The checklist was developed by the researchers based on the literature and evaluated for content validity by 10 nursing faculty members using the Davis technique. Higher scores indicate better urinary catheterization skill performance.

    Time frame: Immediately after the educational intervention

07

Study locations

1 site
  • Toros University
    Mersin, Mersin 33140, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Apr 2025 to primary completion in May 2025, 1 month.

Of 3,841 non-industry interventional studies with no phase under Anxiety Disorders, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 28. This study's 1 month is below that.

Counting every sponsor, half of 3,943 studies reached it within 12 months; a quarter within 5 and three quarters within 28.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 11, 2026
First posted
Sep 17, 2026
StartActual
Apr 10, 2025
Primary completionActual
May 10, 2025
CompletionActual
May 10, 2025
Last update
Oct 1, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Minor edits
Nothing that changes what the study is or who can join. Edited: index terms and conditions
1 update, last Oct 1, 2026
Show all 1 update
  1. Oct 1, 2026
    Minor edits only
    + 2 other changes: index terms and conditions

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
NCT07824362
Lead sponsor
Behire SANÇAR
Responsible party
Behire SANÇAR (Associate Professor, Toros University) — Sponsor-investigator
First posted
Sep 17, 2026
Start date
Apr 10, 2025
Primary completion
May 10, 2025
Completion
May 10, 2025
Last update
Oct 1, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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