- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05469035
The Effect of Nurse Training on the Improvement of Subcutaneous Heparin Applications
Hamidiye Faculty of Nursing, University of Health Sciences
One of the most important duties and responsibilities of nurses is drug administration. During drug administration, the nurse uses appropriate administration techniques and ensures patient safety by knowing the drugs and their side effects. This study aimed to examine the effect of nurse training on the improvement of subcutaneous heparin applications. In this study, it was planned to train nurses by using two different training methods. These methods are online and face-to-face training.
In both methods, it was planned to evaluate the subcutaneous drug administration knowledge and skill of nurses before and after the training.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Demet İnangil
- Phone Number: 05303021160
- Email: demet.inangil@sbu.edu.tr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- volunteering to participate in the study
Exclusion Criteria:
- not have administered subcutaneous heparin in the clinical practice
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental
Nurses in the experimental group participated in mobile-based video learning.
|
Nurses in the experimental group participated in mobile-based video learning.
Other Names:
|
Active Comparator: Control
Nurses in the experimental group participated in face-to-face learning.
|
Nurses in the experimental group participated in face-to-face learning.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Improvement of subcutaneous heparin applications
Time Frame: Through study completion, an average of 1 months
|
The primary outcome of this study is the improvement of nurses' subcutaneous heparin applications.
The 25-item checklist prepared by the researchers based on the literature includes the application steps of subcutaneous heparin knowledge and skill.
|
Through study completion, an average of 1 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Comparision of two different method
Time Frame: Through study completion, an average of 1 months
|
The secondary outcome of this study is the comparison of the two different education methods.The 25-item checklist prepared by the researchers based on the literature includes the application steps of subcutaneous heparin knowledge and skill.
|
Through study completion, an average of 1 months
|
Collaborators and Investigators
Investigators
- Study Chair: Demet İnangil, Istanbul Saglık Bilimleri University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1640
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
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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