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Assessing the Knowledge and Self-confidence of Healthcare Workers to Perform Transurethral Catheterization: A Multicenter Survey

Assessing the Knowledge and Self-confidence of Healthcare Workers to Perform Transurethral Catheterization: A Multicenter Survey

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05334225
Enrollment
1000
Registered
2022-04-19
Start date
2021-09-01
Completion date
2022-12-31
Last updated
2022-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Catheter Complications, Catheter Related Complication, Urethral Catheterization, Urethral Catheterization Related Injury

Brief summary

Rationale: Healthcare professionals regularly perform transurethral catheterization. They may have not sufficient knowledge, experience, and self-confidence about urethral catheterization. This can cause an increased risk of urethral catheterization-related injury and morbidity. With an appropriate training program, we can raise the knowledge and self-confidence of healthcare professionals in performing transurethral catheterization. Primary Objective: To compare knowledge and self-confidence amongst healthcare workers in performing urethral catheterization before and after the proposed urethral catheterization training program. Secondary Objective: To compare the traumatic catheterization rates before and after the proposed urethral catheterization training program. Study design: This study is a prospective multi-center trial using a questionnaire for assessing the healthcare professionals about urethral catheterization knowledge and self-confidence before and after a urethral catheterization training program, where their evaluation is scheduled 6 months after the training. Study population: The study population comprises medical health workers (nurses, paramedics and doctors) from 5 different Medipol Hospitals working at surgical and non-surgical departments. Intervention: An in-person urethral catheterization training program that utilizes training videos (demonstrating procedures, providing examples of ordinary and difficult cases, utilizing animation techniques as well) Main study parameters/endpoints: Primary endpoint is the change in self-reported self-confidence and knowledge in urethral catheterization following the training. The secondary endpoint is the change in complicated/traumatic urethral catheterization following the training. A complicated/traumatic catheterization is defined as a urethral catheterization requiring the intervention of a urologist.

Interventions

OTHERTraining Program

An in-person urethral catheterization training program that utilizes training videos (demonstrating procedures, providing examples of ordinary and difficult cases, utilizing animation techniques as well)

Sponsors

Istanbul Medipol University Hospital
CollaboratorOTHER
Betül Kartal
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Healthcare workers (paramedics, nurses, and doctors) working in the emergency department, intensive care, operating rooms, departments of gynecology, general surgery, urology, orthopedics, neurology, internal medicine, cardiology, and anesthesiology -

Exclusion criteria

Healthcare workers that not working non-clinic services, \-

Design outcomes

Primary

MeasureTime frameDescription
Studying The Reason For Traumatic Catheterization Through Surveys1 yearEvaluating the reason why traumatic catheterization happens (lack of experience, stress, challenging case, wrong equipment, etc.) through surveys prepared for health care workers that are involved in catheterization process.
Reducing The Traumatic Catheterization Case Number Through The Training and Comparison Surveys1 yearAfter the initial survey results, health care workers will go through a special training period for relearning correct catheterization methods. After the training, case numbers will be compared to before the training period and same survey will be distributed again to health care workers to compare their initial and final survey results.

Countries

Turkey (Türkiye)

Contacts

Primary ContactGökhan Çalık
gcalik@medipol.edu.tr+90533 934 38 50
Backup ContactBetül Berşan Kartal
bbkartal@medipol.edu.tr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026