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

Sponsor
Betül Kartal (Other)
Overall Status
Recruiting
CT.gov ID
NCT05334225
Collaborator
Istanbul Medipol University Hospital (Other)
1,000
1
16
62.6

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Training Program

Study Design

Study Type:
Observational
Anticipated Enrollment :
1000 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Assessing the Knowledge and Self-confidence of Healthcare Workers to Perform Transurethral Catheterization: A Multicenter Survey
Actual Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Health Workers

Doctors, nurses, paramedics, midwifes

Other: Training 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)

Outcome Measures

Primary Outcome Measures

  1. Studying The Reason For Traumatic Catheterization Through Surveys [1 year]

    Evaluating 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.

  2. Reducing The Traumatic Catheterization Case Number Through The Training and Comparison Surveys [1 year]

    After 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts 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,

-

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medipol Mega University Hospital Istanbul Bağcılar Turkey 34214

Sponsors and Collaborators

  • Betül Kartal
  • Istanbul Medipol University Hospital

Investigators

  • Study Director: Özgür Arıkan, oarikan@medipol.edu.tr

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Betül Kartal, Research Coordinator/Specialist, Medipol University
ClinicalTrials.gov Identifier:
NCT05334225
Other Study ID Numbers:
  • 10010
First Posted:
Apr 19, 2022
Last Update Posted:
Apr 19, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 19, 2022