The Effect of Care-oriented Practical Training on Nurses' Intensive and Critical Care Competency and HAIs Indicators

April 26, 2024 updated by: Yeliz Karaçar, Akdeniz University

The Effect of Care-oriented Practical Training on Nurses' Intensive and Critical Care Competence and Healthcare-associated Infection Indicators

It was aimed to evaluate the effect of care-oriented practical training on the intensive and critical care competencies of nurses, the hand hygiene compliance rate of nurses and care support staff, and HAI indicators.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Detailed Description

Does care-oriented practical training increase nurses's intensive and critical care competencies? Does care-oriented practical training increase the hand hygiene compliance rate of nurses and care support staff? Does care-oriented practical training reduce HAI indicators in intensive care units?

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
122

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • 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 Locations

  • Turkey
    • Antalya
      • Konyaaltı, Antalya, Turkey, 07070
        • Akdeniz University

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

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Working as a nurse in the Adult Intensive Care Unit
  • Working as a care support staff in an adult intensive care unit
  • Volunteering to participate in research

Exclusion Criteria:

  • Wanting to withdraw from the research
  • Not being able to attend the final test (due to illness, leave, report, etc.)

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: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: Care-oriented group
Care-oriented practical training intervention is a 2-hour care-oriented applied group training program for intensive care nurses in groups of 13-15 people.
Behavioral: Care-oriented Practical Training
The training content includes evidence-based practice recommendations for intensive and critical care, hand hygiene, hygiene practices in patients with special needs, and prevention and control of common HAIs. In the first stage of the training, practical training will be given by the intensive care coordinator and infection control nurse on the application model. In the second stage, patient care practices of a care team consisting of an intensive care nurse and care support staff will be observed. The training will be conducted interactively with narration, demonstration and question and answer techniques.

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Intensive and Critical Care Nursing Competence Scale
Time Frame: Before the Care Oriented Practical Training Intervention (October 2023) and one month after the training (November 2023)
The mean score of Intensive and Critical Care Nursing Competence Scale
Before the Care Oriented Practical Training Intervention (October 2023) and one month after the training (November 2023)
Nurse hand hygiene compliance
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention.
Nurse hand hygiene compliance rate (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention.
Care support staff hand hygiene compliance
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention.
hand hygiene compliance rate (%) of care support staff
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention.
Central catheter-associated bloodstream infections
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Central catheter-associated bloodstream infections rate (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Ventilator-associated Event
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Ventilator-associated Event rate (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Catheter-associated Urinary Tract Infections
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Catheter-associated Urinary Tract Infections rate (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Klebsiella spp.
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Klebsiella spp. n (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Enterococcus spp.
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Enterococcus spp.n (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Acinetobacter spp
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Acinetobacter spp. n (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Pseudomonas spp.
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Pseudomonas spp. n (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Enterobacterales
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Enterobacterales, n (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Candida
Time Frame: Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention
Candida, n (%)
Health care-associated infection indicators in the intensive care unit 3 months before the Care-Oriented Practical Training Intervention and 3 months after the intervention

Collaborators and Investigators

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

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Akdeniz University

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Director: Şenay TAKMAK, Asst. Prof., Kutahya Health Sciences University

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)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
October 16, 2023

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
January 31, 2024

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
February 1, 2024

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
January 26, 2024

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
January 26, 2024

First Posted (Actual)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
February 2, 2024

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
April 29, 2024

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
April 26, 2024

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
April 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • KAEK-800

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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