- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05853588
The Effect Of Training On Nursing Qualıty
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
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Antakya
-
Istanbul, Antakya, Turkey
- Istanbul Univercity-Cerrahpasa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
Investigators
- Study Director: Betül SÖNMEZ, Ass. prof, betul.sonmez@iuc.edu.tr
Publications and helpful links
General Publications
- Heslop L, Lu S, Xu X. Nursing-sensitive indicators: a concept analysis. J Adv Nurs. 2014 Nov;70(11):2469-82. doi: 10.1111/jan.12503. Epub 2014 Aug 12. Erratum In: J Adv Nurs. 2019 Dec;75(12):3844.
- Driscoll A, Grant MJ, Carroll D, Dalton S, Deaton C, Jones I, Lehwaldt D, McKee G, Munyombwe T, Astin F. The effect of nurse-to-patient ratios on nurse-sensitive patient outcomes in acute specialist units: a systematic review and meta-analysis. Eur J Cardiovasc Nurs. 2018 Jan;17(1):6-22. doi: 10.1177/1474515117721561. Epub 2017 Jul 18.
- Donabedian A. The quality of care. How can it be assessed? JAMA. 1988 Sep 23-30;260(12):1743-8. doi: 10.1001/jama.260.12.1743.
- Cavazza, N. & Serpe, A. 2010, The Impact of Safety Training Programs on Workers' Psychosocial Orientation and Behaviour. Revue internationale de psychologie sociale, 23, 187-210.
- Amiri M, Khademian Z, Nikandish R. The effect of nurse empowerment educational program on patient safety culture: a randomized controlled trial. BMC Med Educ. 2018 Jul 3;18(1):158. doi: 10.1186/s12909-018-1255-6.
- Burke MJ, Sarpy SA, Smith-Crowe K, Chan-Serafin S, Salvador RO, Islam G. Relative effectiveness of worker safety and health training methods. Am J Public Health. 2006 Feb;96(2):315-24. doi: 10.2105/AJPH.2004.059840. Epub 2005 Dec 27.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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