- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06370364
Nurses' Practice of Safe Blood Transfusion in Surgical and Critical Care Units
April 14, 2024 updated by: Nagah Abd El-Fattah Mohamed Aly, Matrouh University
Contributing Factors Affecting Nurses' Practice of Safe Blood Transfusion in Surgical and Critical Care Units
Blood transfusions are an important part of nursing procedure.
Nurses play a key role in safely administering blood products to patients in surgical and critical care unit
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The aim of the study was to evaluate nurses' employment conditions as contributing factors affecting nurses' practice of safe blood transfusion in surgical and critical care units in Alexandria Main University Hospital.
Study Type
Observational
Enrollment (Actual)
350
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
-
-
-
Mersa Matruh, Egypt, 002
- Faculty of Nursing, Matrouh University
-
-
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
Sampling Method
Probability Sample
Study Population
A convenience sampling was utilized to recruit 350 nurses from surgical and critical care units
Description
Inclusion Criteria:
Nurses
- willing to participate in the study
- work in surgical and critical care units
- Sign a consent
Exclusion Criteria:
Nurses
- Work in outpatient units and other units
- Did not sign a consent
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Questionnaire to measure factors affecting safe blood transfusion
Time Frame: one month
|
Factors affecting safe blood transfusion as assessed using a binary scale (Yes=1 and No=0)
|
one month
|
|
observational checklist to measure nurses' practice of safe blood transfusion
Time Frame: three months
|
Nurses' practice of safe blood transfusion as assessed using scoring of the practice checklist (zero score for not done, 0.5 score for incompletely done and one score for completely done).
|
three months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Wael M. Lotfy, Ph.D, Faculty of Nursing, Matrouh University, Egypt
- Principal Investigator: Nagah Abd El-Fattah Mohamed Aly, Ph.D, Faculty of Nursing, Matrouh University, Egypt
- Study Chair: Safaa M. El-Shanawany, Ph.D, Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Alexandria University, Egypt
- Study Chair: Maha Ghanem, Ph.D, Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Alexandria University, Egypt
- Principal Investigator: Hanaa Abbass, Ph.D, Faculty of Nursing, Matrouh University , Egypt
- Principal Investigator: Maysa Elbiaa, Ph.D, Faculty of Nursing, Matrouh University , Egypt
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)
December 1, 2020
Primary Completion (Actual)
April 30, 2021
Study Completion (Actual)
April 30, 2021
Study Registration Dates
First Submitted
April 14, 2024
First Submitted That Met QC Criteria
April 14, 2024
First Posted (Actual)
April 17, 2024
Study Record Updates
Last Update Posted (Actual)
April 17, 2024
Last Update Submitted That Met QC Criteria
April 14, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 25
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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