- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06371066
The Effect of Video-based Training on the Knowledge Levels of Nursing Students
The Effect of Video-based Training on the Knowledge Levels of Nursing Students: A Randomized Controlled Trial
Study Overview
Status
Intervention / Treatment
Detailed Description
This pretest-posttest randomized controlled experimental study was designed as a randomized controlled parallel designed trial.
This study was conducted at the nursing department of a state university. The population of the study consisted of second-year nursing students who enrolled in the Surgical Nursing course. The study was conducted with students who met the inclusion criteria in the study without any sample calculation. Class size was 100 and 97 of them agreed to participate in the study. The students were assigned to the VBT group or the traditional training group via a stratified randomization method in order to ensure the balance between the groups. The study was carried out with 49 experimental and 48 control groups. After the students were divided into two groups according to gender, an equal number of male and female students were assigned to the experimental and control groups by drawing lots, one of the simple random sampling methods. The student participants were randomly assigned to one of the two groups using a random number table. To avoid bias in this randomized controlled study, assignments to the groups were made by an outside researcher. All training sessions were carried out by researchers. Dependent variables of the research project are; students' level of knowledge, and the independent variables are student information data. Data collection forms (student information, knowledge levels) developed by researchers using the literature
Video scenario: It consisted of a preoperative patient case, learning objectives for nursing care, the content of the scenario and the roles. The scenario involved one 65-year-old female patient who had weight loss, loss of appetite, abdominal pain, and bloating for preoperative preparation of left hemicolectomy surgery. It has been prepared by the formal education given within the scope of the surgical nursing course. The scenario was designed with careful consideration given to conceptual, psychological, and physical realities. The content validity of scenario was assessed by four expert nursing faculty members.
İmplementation: The training was presented to the experimental group by video, and to the control group by the traditional method (using a lecture-style PowerPoint presentation with supporting visual components, question-answer, and narrative method). Before the training, both groups answered the "The Student Information Form" and "The Knowledge Form" and were informed about the purpose of the course, learning objectives and outcomes, and scenario roles, and their questions were answered. The students were informed that their involvement in the research was voluntary and had no bearing on their course grades no academic credit would be given for participating. At the end of the training of both groups, all the scenario was discussed with the students, and their questions were answered. Right after training (post-test 1) and three weeks later (post-test 2: two weeks after post-test 1), the students answered 'The Knowledge Form'.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Kirikkale, Turkey
- Kirikkale University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- willingness to participate in the study,
- taking no previous surgical nursing course.
Exclusion Criteria:
- unwillingness to participate in the study
- having no previous knowledge and experience in surgical nursing
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
video-based training group
|
the experimental group was educated by video
Other Names:
|
|
Other: Control group
traditional formal training group
|
the control group was educated by traditional formal training
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Student Information Form
Time Frame: one day
|
This form was developed by the researchers in accordance with the literature.
It consisted of 12 questions about individual (age, gender, economic status), academic (graduated high school), and experiencing video in daily life (taking VBT before, status and frequency of watching training videos on the internet) characteristics.
|
one day
|
|
The Knowledge Form for Preoperative Patient Preparation
Time Frame: one day
|
This form was prepared by the researchers in line with the literature.
The form consisted of 25 items with three options (True, False, Not know).
Each right answer was given one points, while each wrong and not known answer was given zero points.
The total test score ranged from zero to 25. High scores indicated a high level of knowledge.
In order to evaluate whether it looked or read like the construct aiming to measure the level of knowledge of preoperative education and patient preparation on the day of surgery was assessed by four expert nursing faculty members.
The form was revised and finalized in line with expert evaluations.
|
one day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Atiye Erbaş, PhD, Duzce University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- EAkyuz-2
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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