The Effect Of Training On Nursing Qualıty

May 2, 2023 updated by: Bircan Kara, Istanbul University - Cerrahpasa (IUC)

The Effect Of Toolbox Trainings On Nursing Sensitive Quality Indıcators

The aim of this study, in a randomized controlled design with pretest, posttest and control groups, is to determine the effect of on-the-job (toolbox) training given to nurses on nursing-sensitive quality indicators (pain management, pressure sores, patient falls, Peripheral Venous Catheter complications and adverse event reporting). it aims to answer are:

- Does toolbox training have an effect on nursing-sensitive quality indicators? After the training, participants are expected to adapt to quality practices.

This study consists of experimental and control groups. Experimental and control groups were determined by drawing lots with the help of an external expert. Nurses who met the inclusion criteria were included in the lottery.

Inclusion criteria for the experimental and control groups were determined as follows:

  • Working in one of the hospital's internal medicine or surgical services
  • Having been working in the current service for at least 6 months, apart from past work experience
  • Having completed the orientation process to the hospital and taking responsibility for patient care
  • Voluntarily agree to participate in the study

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study was carried out to determine the effect of toolbox training on nursing-sensitive quality indicators (pain management, pressure sores, patient falls, peripheral venous catheter complications and adverse event reporting) in a randomized controlled, pre-test, post-test, experimental and control group design.

The population of the study consisted of nurses working in the inpatient services (except the intensive care units) of a training and research hospital in Hatay. A total of 77 nurses working in the experimental and control group services determined by randomization constituted the sample of the research (experimental group: 38 nurses, control group: 39 nurses).

Study Type

Interventional

Enrollment (Actual)

77

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 Locations

    • Antakya
      • Istanbul, Antakya, Turkey
        • Istanbul Univercity-Cerrahpasa

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

No

Description

Inclusion Criteria:

  • Working in one of the hospital's internal medicine or surgical services
  • Being working in the current service for at least 6 months apart from past work experience
  • Having completed the orientation process to the hospital and taking responsibility for patient care
  • To voluntarily agree to participate in the study

Exclusion Criteria:

  • Participants who did not meet the inclusion criteria were excluded.

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group
It was determined by lot by the volunteer nurses who accepted to participate in the study.
On-the-job (toolbox) training given to the experimental group and containing brief information, lasting at most 10 minutes
No Intervention: Control group
It was determined by lot by the volunteer nurses who accepted to participate in the study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nurse Information Form
Time Frame: before the training
This form consists of 10 questions in total to determine the demographic study characteristics of the nurses participating in the research.
before the training
Nursing Sensitive Quality Indicators Application Information Form (pretest-posttest)
Time Frame: before the training
Both groups were applied before the on-the-job training to be given to the experimental group and after all trainings were completed. It was prepared in the light of current literature in order to determine the knowledge level of nurses in the experimental and control groups about nursing-sensitive quality indicators and to evaluate the effectiveness of on-the-job training given to the experimental group. A minimum of 0 and a maximum of 100 points can be obtained from this test.
before the training
Nursing Sensitive Quality Indicators Implementation Checklists
Time Frame: before the training
The checklists developed in line with the literature have been developed for the management of pain in the unit, pressure ulcer, risk of falling, Peripheral Venous Catheter complications and adverse event reporting, and consist of five sections.In this test, 1 point is given for each complete application.
before the training
Unit Quality Indicators Monitoring Form
Time Frame: before the training
Data on 5 nursing-sensitive quality indicators (fall rates (in percent), patient rate with correct pain management (as a number), pressure ulcer rates (in percent), Peripheral Venous Catheter complication (as a number) and adverse event reporting rates(in percent) ) followed before and after the training, and data on the average number of hospitalization days are included.
before the training

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nursing Sensitive Quality Indicators Application Information Form (pretest-posttest)
Time Frame: At 8 weeks after give all trainings
Both groups were applied before the on-the-job training to be given to the experimental group and after all trainings were completed. It was prepared in the light of current literature in order to determine the knowledge level of nurses in the experimental and control groups about nursing-sensitive quality indicators and to evaluate the effectiveness of on-the-job training given to the experimental group. A minimum of 0 and a maximum of 100 points can be obtained from this test.
At 8 weeks after give all trainings
Nursing Sensitive Quality Indicators Implementation Checklists
Time Frame: At 8 weeks after give all trainings
The checklists developed in line with the literature have been developed for the management of pain in the unit, pressure ulcer, risk of falling, Peripheral Venous Catheter complications and adverse event reporting, and consist of five sections.In this test, 1 point is given for each complete application.
At 8 weeks after give all trainings
Unit Quality Indicators Monitoring Form
Time Frame: At 8 weeks after give all trainings
Data on 5 nursing-sensitive quality indicators (fall rates (in percent), patient rate with correct pain management (as a number), pressure ulcer rates (in percent), Peripheral Venous Catheter complication (as a number) and adverse event reporting rates(in percent) ) followed before and after the training, and data on the average number of hospitalization days are included.
At 8 weeks after give all trainings

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nursing Sensitive Quality Indicators Implementation Checklists
Time Frame: At the 12th week after all trainings are completed
The checklists developed in line with the literature have been developed for the management of pain in the unit, pressure ulcer, risk of falling, Peripheral Venous Catheter complications and adverse event reporting, and consist of five sections.In this test, 1 point is given for each complete application.
At the 12th week after all trainings are completed
Unit Quality Indicators Monitoring Form
Time Frame: At the 12th week after all trainings are completed
Data on 5 nursing-sensitive quality indicators (fall rates (in percent), patient rate with correct pain management (as a number), pressure ulcer rates (in percent), Peripheral Venous Catheter complication (as a number) and adverse event reporting rates(in percent) ) followed before and after the training, and data on the average number of hospitalization days are included.
At the 12th week after all trainings are completed

Collaborators and Investigators

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

Investigators

  • Study Director: Betül SÖNMEZ, Ass. prof, betul.sonmez@iuc.edu.tr

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)

November 1, 2021

Primary Completion (Actual)

July 30, 2022

Study Completion (Actual)

December 30, 2022

Study Registration Dates

First Submitted

April 12, 2023

First Submitted That Met QC Criteria

May 2, 2023

First Posted (Estimate)

May 11, 2023

Study Record Updates

Last Update Posted (Estimate)

May 11, 2023

Last Update Submitted That Met QC Criteria

May 2, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • IstanbulUCerrahpaşabkara

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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