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IRCT20200626047926N1 IRCT 2020-06-28 Universiti Putra Malaysia Effect of Trauma triage program among emergency nurses ATLS (Advance Trauma Life Support) Effectiveness of a Trauma Triage Educational Intervention on Knowledge and Skill among Emergency Nurses in Public Hospitals in the West Bank, Palestine 2020-10-01 anticipated 114 Complete https://irct.ir/trial/49209 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: The first box will consist of each selected hospital in small pieces of paper that are covered, while the second box will consist of either experimental or control groups also written in small pieces of paper and covered. Next, randomly will draw from the first box to determine the hospital and likewise from the second box to determine whether it be experimental or control group by lottery method. Then randomly will draw the second paper from the first box to determine the hospital while for the second box it will automatically be the remaining paper to determine whether it be experimental or control group, Blinding description: Dr. Sajed Faisal Ghawadra will be helped during the intervention and doing the lottery method to avoid the bias and control the confounder. Thus, the hospital, participants, researcher, and trainer (Dr. Belal H. Rawajbeh) are blinded. This study will be recorded the intervention and lottery method by videos and share them with the researchers at the end of data analysis to make sure the program and lottery method were done in the right way. In this study, the trial will be a double-blind trial, and therefore, the hospital, participants, researcher, and trainer are blinded. They will not aware of the random allocation or the hypothesis that is tested until the intervention will finish. The study design, measurements, and population. N/A Trauma. Intervention 1: Intervention group: The intervention group will receive 2 days of ATLS. It will measure at pre, post, and 12 weeks follow-up of intervention. Intervention 2: Control group: the control group will receive 2 days of needle stick injury lectures. It will measure at pre, post, and 12 weeks follow-up of intervention. Yes - There is a plan to make this available What will be shared: The information obtained from this study will allow you to know your existing level of knowledge and skills in trauma triage. For those selected to participate in the second phase of the study, you will be able to upgrade and improve your knowledge and skills via the intervention program. When: It will start on1st of October 2020 - 30 of September 2021 To whom: The information of this study will be available for a researcher who seeks emergency field Conditions: SPSS, Chi-square, repeated measure ANOVA. the supervisors will review the data individually. Where to obtain: online journals, UPM Library. How to obtain: The questionnaire will be kept for a maximum period of one year until the end of the analysis and discussion of the results, and it will be placed in a sealed envelope inside a locked cabinet. Further, the soft copy and data will be stored in a computer with a username and password and accessible only by the main researcher and my supervisor. Confidentiality will be maintained by assigning a code instead of the name. After the lapse of one year. Comments: no comment
public Khalaf Abdelfattah Mohd Awwad
serdang hosital street, serdang, kl
Jenin Palestine, State of 43300 +60 3-8947 2395 gs55200@student.upm.edu.my University Putra Malaysia scientific Khalaf Abdelfattah Moh Awwad
serdang hosital street, serdang, kl
Kuala Lumpur Malaysia 43300 +60 3-8947 2395 gs55200@student.upm.edu.my Universiti Putra Malaysia Malaysia Nurses in the emergency department with fully employed in the selected for the experimental and control hospitals with at least one year working experience in the emergency department. It also will be included those who are available for the research study and those who do not on leave or retire during this study. Emergency nurses in Public hospital affiliated to the Palestinian Ministry of Health. Emergency nurses who are less than 60 years old. Emergency nurses who had not trained on trauma triage. no limit 60 years Both Jerusalem hospitals in the West Bank will be excluded with reason unsafe city in phases one and two of this study. The hospitals have moderate or high knowledge and skills in phase one will be excluded in phase two of this study. G89.11 Acute pain due to trauma Prevention Placebo Intervention group: The intervention group will receive 2 days of ATLS. It will measure at pre, post, and 12 weeks follow-up of intervention. Control group: the control group will receive 2 days of needle stick injury lectures. It will measure at pre, post, and 12 weeks follow-up of intervention. Determine and compare the mean of differences in the emergency nurses’ knowledge and skill at pre, post, and 3 months follow-up within and between the experimental and control groups of intervention. Timepoint: This study will measure the variables at pre, post, and 12 weeks follow-up of intervention. Method of measurement: Repeated measures ANOVA will measure the comparison of differences in means of the emergency nurses’ knowledge and skill scores between and within the experimental and control groups at pre, post, and 3 months follow-up of intervention. Universiti Putra Malaysia Approved 2020-05-20 Ethics Committee for Research involving Human Subjects, (JKEUPM) at Universiti Putra Malaysia (UPM) serdang hosital street, serdang, kl Kuala Lumpur Serdang Malaysia