The Effect Of Training On Nursing Qualıty

Sponsor
Istanbul University - Cerrahpasa (IUC) (Other)
Overall Status
Completed
CT.gov ID
NCT05853588
Collaborator
(none)
77
1
2
13.9
5.5

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: training
N/A

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 Design

Study Type:
Interventional
Actual Enrollment :
77 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This study in randomized controlled, pretest, posttest and experiment, control group designThis study in randomized controlled, pretest, posttest and experiment, control group design
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
The Effect Of Toolbox Trainings On Nursing Sensitive Quality Indıcators
Actual Study Start Date :
Nov 1, 2021
Actual Primary Completion Date :
Jul 30, 2022
Actual Study Completion Date :
Dec 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

It was determined by lot by the volunteer nurses who accepted to participate in the study.

Other: training
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.

Outcome Measures

Primary Outcome Measures

  1. Nurse Information Form [before the training]

    This form consists of 10 questions in total to determine the demographic study characteristics of the nurses participating in the research.

  2. Nursing Sensitive Quality Indicators Application Information Form (pretest-posttest) [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.

  3. Nursing Sensitive Quality Indicators Implementation Checklists [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.

  4. Unit Quality Indicators Monitoring Form [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.

Secondary Outcome Measures

  1. Nursing Sensitive Quality Indicators Application Information Form (pretest-posttest) [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.

  2. Nursing Sensitive Quality Indicators Implementation Checklists [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.

  3. Unit Quality Indicators Monitoring Form [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.

Other Outcome Measures

  1. Nursing Sensitive Quality Indicators Implementation Checklists [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.

  2. Unit Quality Indicators Monitoring Form [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 İstanbul Univercity-Cerrahpaşa Istanbul Antakya Turkey

Sponsors and Collaborators

  • Istanbul University - Cerrahpasa (IUC)

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Bircan Kara, PhD Stıdent, Istanbul University - Cerrahpasa (IUC)
ClinicalTrials.gov Identifier:
NCT05853588
Other Study ID Numbers:
  • IstanbulUCerrahpaşabkara
First Posted:
May 11, 2023
Last Update Posted:
May 11, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Bircan Kara, PhD Stıdent, Istanbul University - Cerrahpasa (IUC)

Study Results

No Results Posted as of May 11, 2023