Digital Storytelling in Pediatric Safe Drug
The Efficiency of Education Given to Students With Digital Storytelling in Safe Pediatric Intravenous Drug Administration
1 other identifier
interventional
84
1 country
1
Brief Summary
Summary Aim: This research was conducted to determine the effectiveness of education given to students using digital storytelling in safe pediatric intravenous drug administration. Method: It is a randomized controlled experimental study. The sample of the study consisted of 84 nursing students. The students included in the study were divided into two equal groups: the experimental and control groups. Digital education material of the experimental group and theoretical education was applied to the control group. Before and after the training, a post-knowledge test was made and evaluated.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 8, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
April 6, 2023
CompletedFirst Submitted
Initial submission to the registry
April 17, 2023
CompletedFirst Posted
Study publicly available on registry
May 6, 2023
CompletedMay 6, 2023
May 1, 2023
5 months
April 17, 2023
May 4, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Statistical difference between groups about knowledge test scores
Safe pediatric drug practices knowledge test is applied twice as pre-test and post-test in experimental and control groups. Safe pediatric drug practices knowledge test: It is a 17-question form prepared by researchers. Content validity has been made for the form. Each correct answer is calculated as 1 point and each wrong answer is calculated as 0 points. The higher the score obtained from the questionnaire, the higher the level of knowledge.
During the education, approximately 25 minutes
Study Arms (2)
Digital Education Group
EXPERIMENTALAll participants in this group were given the "Safe pediatric intravenous drug administration knowledge test" prepared by the researchers as a pre-test. The participants of this group, who were determined by randomization, were given training prepared using the digital storytelling method. The training took 25 minutes. After the training, the "Safe intravenous drug administration knowledge test" was applied as a post-test.
Control Group
NO INTERVENTIONNo intervention was made. All participants in this group were given the "Safe pediatric intravenous drug administration knowledge test" prepared by the researchers as a pre-test. Afterward, theoretical information on the subject was given. After theoretical information, the "Safe intravenous drug administration knowledge test" was applied as a post-test.
Interventions
Providing training on safe pediatric intravenous drug administration with digital storytelling method
Eligibility Criteria
You may qualify if:
- Being a student of the Department of Nursing
- Taking the child health and diseases nursing course and being successful
- Volunteering to participate in the research
You may not qualify if:
- Participate and quit the study
- Being a 1st and 2nd year nursing student
- Failure of the child health and diseases nursing course
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ege Universitylead
- Izmir Bakircay Universitycollaborator
Study Sites (1)
Semih
Izmir, 35665, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Semih Akkoyun
Izmir Bakircay University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant professor
Study Record Dates
First Submitted
April 17, 2023
First Posted
May 6, 2023
Study Start
December 8, 2021
Primary Completion
April 30, 2022
Study Completion
April 6, 2023
Last Updated
May 6, 2023
Record last verified: 2023-05
Data Sharing
- IPD Sharing
- Will not share
The study will be prepared for publication