- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05762341
Pressure Injury Training With a Blended Approach Learning Approach on Care Behaviors of Intensive Care Nurses
March 29, 2023 updated by: Ebru Kiraner, Istanbul University - Cerrahpasa (IUC)
Istanbul University Cerrahpaşa Graduate Education Institute, PhD Student
By saving life or delaying death, the length of stay of the patient in the intensive care unit is prolonged, and this leads to the emergence of other problems in addition to the disease in the patient.
Pressure injuries are one of these problems.
Although many internationally accepted pressure injury prevention guidelines are available, it is frequently reported that there is no significant reduction in pressure injury prevalence.
It has been emphasized in the literature that nurses do not have enough knowledge about the prevention of pressure injury.
"Blended Learning", in which technologies such as web-based, e-learning and m-learning are used together with face-to-face education, is an effective approach in realizing learning outcomes.
This approach facilitates the achievement of the educational program's objectives by integrating the positive aspects of web-assisted learning and face-to-face learning.
In the light of these explanations, it is aimed to examine the effect of pressure injury prevention training given with the blended learning approach on the care behaviors of intensive care nurses.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The research was planned in a mixed design with a qualitative dimension in terms of determining the experimental and training needs, using the focus group interview method in the evaluation of the program, with the aim of examining the effect of pressure injury prevention training given with the blended learning approach on the care behaviors of intensive care nurses.The universe of the study consists of a total of 100 nurses working in the 3rd Level intensive care units of Istanbul University-Cerrahpaşa Cerrahpaşa Faculty of Medicine.
The sample size of the study was calculated by using power analysis.
Since the differences between the experimental and control groups before and after the experiment were examined comparatively in the research, ANOVA will be made for mixed measurements.
Accordingly, the sample size was calculated by keeping the effect size (Cohen's f) 0.25, that is, at a medium level, based on the expected averages and standard deviations of the groups.
G*Power 3.1.9.4 software (Faul, Erdfelder, Lang & Buchner, 2007) was used for the calculation.
In order to make a decision with 95% confidence for Type I, the expected power of α error was 0.05 and for Type II error 1-β expected power was 0.80.
When the number of groups was entered as 2 (experiment, control), the number of measurements was 2 (pretest, posttest), the expected correlation between repeated measurements was 0.5, and the ε correction was 1, the expected total sample size for this study was calculated as 34 people.
Accordingly, there will be a total of 44 people in the research, 17 people in the experimental and control groups, taking into account the possibility of data loss.
In order to prevent interaction between the groups in the formation of the experimental and control groups, it will be randomly assigned by paying attention to the fact that the experimental group is from one unit and the control group is from the other unit.
Homogenization will be achieved between the groups in terms of having an intensive care nursing certificate, age, years of experience, years of working in intensive care, and Knowledge Evaluation Scale score in Preventing Pressure Ulcers.
It will be collected by the researcher and the nurse in charge of the unit by using the Nurse Information Form, the Information Evaluation Scale in Pressure Ulcer Prevention, the Pressure Injury Prevention Efficiency Evaluation Form, the Training Program Evaluation Form, the Semi-Structured Interview Form before the Training Program, and the Semi-Structured Interview Form after the Training Program.
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
-
Istanbul, Turkey
- Istanbul University Cerrahpasa Hospital
-
-
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
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Adult intensive care nurses working in the Third Level intensive care unit,
- have not received pressure injury training in the last year,
- voluntarily agree to participate in the study will be included.
Exclusion Criteria:
- Nurses who received pressure injury training in the last year
- work in the pediatric intensive care unit and neonatal intensive care unit
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: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: EXPERIMENT GROUP
BOTH GROUPS WILL RECEIVE PRESSURE INJURY PREVENTION TRAINING.
ONLY EXPERIMENTAL GROUP WILL USE THE MOBILE LEARNING TOOL
|
PREVENTION OF PRESSURE INJURY TO FACE TO FACE TRAINING
|
|
Experimental: CONTROL GROUP
BOTH GROUPS WILL RECEIVE PRESSURE INJURY PREVENTION TRAINING.
ONLY EXPERIMENTAL GROUP WILL USE THE MOBILE LEARNING TOOL
|
PREVENTION OF PRESSURE INJURY TO FACE TO FACE TRAINING
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
INCREASE IN PRESSURE INJURY PREVENTION BEHAVIOR SCORES
Time Frame: 3 MONTHS LATER
|
INCREASED BEHAVIOR SCORES TO BE TAKEN FROM THE PRESSURE INJURY PREVENTION QUALIFICATION FORM
|
3 MONTHS LATER
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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)
March 1, 2023
Primary Completion (Actual)
March 14, 2023
Study Completion (Actual)
March 15, 2023
Study Registration Dates
First Submitted
February 28, 2023
First Submitted That Met QC Criteria
February 28, 2023
First Posted (Actual)
March 9, 2023
Study Record Updates
Last Update Posted (Actual)
March 31, 2023
Last Update Submitted That Met QC Criteria
March 29, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IUC Gradu Educ Inst
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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