The Effect of Catheter-Associated Infection Control Training

December 9, 2023 updated by: Elif Gezginci, Saglik Bilimleri Universitesi

The Effect of Catheter-Associated Infection Control Training on Surgical Nurses' Knowledge and Attitude Levels

The goal of this type of study: clinical trial is to determine the effectiveness of educational practices on catheter-associated infection control measures on surgical nurses. The main question it aims to answer are:

  • Is there a difference between the knowledge and attitude levels of surgical nurses receiving and not receiving catheter-related infection control training on preventing peripheral and central catheter-related bloodstream infections?
  • Is there a difference between the knowledge and attitude levels of surgical nurses receiving and not receiving catheter-related infection control training to prevent catheter-related urinary tract infections?

The main tasks that the participants will be asked to do will be explained and their consent will be obtained. The two research groups will be compared.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

This study will be conducted with a total of 70 nurses working in the surgical clinics of a city hospital in Istanbul and meeting the inclusion criteria. Nurses who meet the inclusion criteria of the study will be divided into two groups: intervention (n=35) and control group (n=35) according to the randomization method created with computer-based random numbers. Nurses in the intervention group will be given face-to-face training on evidence-based catheter-related infection control measures. The content of the training program will also be given to the participants as written material (brochure). The training will take an average of 30 minutes. Routine in-service training practices will be given to the control group. Descriptive Characteristics Form, the Peripheral and Central Venous Catheter-Related Bloodstream Infection Prevention Knowledge and Attitudes Scale, and Catheter-Associated Urinary Tract Infections Control Precautions will be used in data collection. Data will be collected from all participants before, immediately after, and three months after the training practices.

Study Type

Interventional

Enrollment (Estimated)

70

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 Contact

Study Contact Backup

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being a nurse
  • Working in the surgical unit
  • Agreeing to participate in the research

Exclusion Criteria:

  • Being on leave/reported (maternity leave, unpaid leave, medical report, etc.)
  • Not filling out the questionnaire

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Intervention Group
Nurses in the intervention group will be given face-to-face training on evidence-based catheter-related infection control measures. The content of the training program will also be given to the participants as written material (brochure). The training will take an average of 30 minutes. After the data collection forms are applied to the participants in the intervention group (pre-test), evidence-based training on catheter-related infection control measures will be conducted. The forms will be applied again immediately after the training (post-test) to measure the knowledge level of nurses and three months after the training (post-test) to measure the level of attitude.
Structured catheter-related infection control training was prepared by using evidence-based information and receiving 10 expert opinions. This training will be given to the participants with a face-to-face PowerPoint presentation by the infection control nurse (researcher) and will also be presented as written material.
No Intervention: Control Group
Routine in-service training practices will be given to the control group. Data collection forms will be applied to the participants in the control group at the same time as the intervention group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The peripheral and central venous catheter-related bloodstream infection prevention knowledge and attitudes of the surgical nurses"
Time Frame: 0-3 months
There is a difference between 0-3 months on the knowledge and attitudes of the training given to nurses to prevent peripheral and central venous catheter-related bloodstream infections. The Peripheral and Central Venous Catheter-Related Bloodstream Infection Prevention Knowledge and Attitudes Scale will be administered to the all participants before the training (pre-test). This scale will be used again immediately after the training (post-test) to measure the knowledge level of nurses and three months after the training (post-test) to measure the level of attitude. The scale includes 14 items and consists of "general precautions" and "catheter care" sub-dimensions. The scale score range is 14-70 points. Higher scores on the scale indicates higher knowledge and attitude.
0-3 months
The catheter-associated urinary tract infections control precautions knowledge and attitudes of the surgical nurses
Time Frame: 0-3 months
There is a difference between 0-3 months on the knowledge and attitudes of the training given to nurses to prevent catheter-associated urinary tract infections. The Catheter-Associated Urinary Tract Infections Control Precautions Scale will be administered to the all participants before the training (pre-test). This scale will be used again immediately after the training (post-test) to measure the knowledge level of nurses and three months after the training (post-test) to measure the level of attitude. The scale includes 15 items and consists of "standard precautions", "maintenance of the closed drainage system" and "catheter-bag change" sub-dimensions. The scale score range is 15-75 points. Higher scores on the scale indicates higher knowledge and attitude.
0-3 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Habibe Filiz Akdemir, RN, Saglik Bilimleri Universitesi

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)

January 25, 2023

Primary Completion (Actual)

June 20, 2023

Study Completion (Estimated)

December 30, 2023

Study Registration Dates

First Submitted

December 19, 2022

First Submitted That Met QC Criteria

January 2, 2023

First Posted (Actual)

January 4, 2023

Study Record Updates

Last Update Posted (Estimated)

December 12, 2023

Last Update Submitted That Met QC Criteria

December 9, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

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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