- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06494267
Video-Assisted Self-Assessment on Nasogastric Tube Insertion
The Effect of Video-Assisted Self-Assessment on Nasogastric Tube Insertion Knowledge and Skills: A Randomized Controlled Trial
Introduction and Purpose Advancements in Nursing Education: The integration of technology, specifically video-supported training, is a significant development in nursing education.
Focus on Nasogastric Tube (NGT) Placement: Proper placement of NGT is a critical skill in nursing. Traditional methods alone may not suffice in acquiring and maintaining this skill.
Objective: Evaluate the impact of video-supported self-assessment on the knowledge and skills of nursing students regarding NGT placement.
Hypotheses Video-supported self-assessment increases students' knowledge about NGT placement.
Video-supported self-assessment enhances students' skills in NGT placement. Materials and Methods Design: A randomized controlled pre-test and post-test experimental design. Ethics: Ethical approval will be obtained and registered with Clinical Trials ID.
Data Collection Tools:
FR.1 Personal Information Form: Demographic data collection. FR.2 NGT Placement Knowledge Test: 20 multiple-choice questions based on theoretical content.
FR.3 NGT Placement Skill Checklist: 51 steps evaluating correct, incorrect, and unobserved applications.
Data Collection Process Initial Phase: Explanation of the study, informed consent, and completion of the FR.1 form and FR.2 pre-test.
Traditional Teaching: A theoretical lecture on NGT placement.
Practical Application:
Experimental Group: Practical demonstration recorded and shared with students for self-assessment.
Control Group: Practical demonstration recorded but not shared with students. Post-Intervention Assessment: FR.2 post-test and an OSCE exam based on FR.3 for both groups after one week.
Data Analysis Software: SPSS 23.0. Methods: T-tests, Chi-square tests, Pearson and Spearman correlation analyses depending on data distribution.
Statistical Significance: p<0.05. Study Limitations Scope: Limited to first-year nursing students at one university. Interaction: Potential interaction between intervention and control group students.
Ethical Principles Approval: Obtained from the Ethics Committee and the university. Participant Rights: Informed consent, respect for autonomy, confidentiality, and adherence to the Helsinki Declaration.
This summary captures the essence of the research study described in the original document, focusing on the purpose, methods, data collection, analysis, limitations, and ethical considerations.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Bahar Çiftçi
- Phone Number: 05068517847
- Email: bahar.ciftci@atauni.edu.tr
Study Contact Backup
- Name: Burak Yavuz
- Phone Number: 05078869275
- Email: burak.yavuz@atauni.edu.tr
Study Locations
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-
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Erzurum, Turkey, 25000
- Recruiting
- Ataturk University Faculty of Nursing
-
Contact:
- BAHAR Çiftçi
- Phone Number: 05068517857
- Email: bahar.ciftci@atauni.edu.tr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being 18 years of age or older
- Being a first-year student at the Faculty of Nursing
- Being taking the Fundamentals of Nursing course for the first time
- Not coming as a horizontal or vertical transfer
- Not being absent on the dates when the research data will be collected
- Being willing to participate in the research and giving written consent
Exclusion Criteria:
- Those who are not first-year nursing students
- Students who come via horizontal or vertical transfer
- Students who graduated from Health Vocational High School
- Students in the intervention group who are not subject to video-assisted self-assessment method
- Students who want to leave the study for any reason during the research process
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental
Students will be videotaped while performing a nasogastric tube placement and will be asked to make a self-assessment.
|
Students in the experimental group will be videotaped while practicing and students will make self-evaluations.
|
|
No Intervention: Control
No application will be made.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
FR.1 Personal Information Form:
Time Frame: 3months
|
This form was prepared by the researchers and consists of 15 questions questioning the demographic characteristics of the students such as age, gender, socioeconomic level, etc.
|
3months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
FR.2 Nasogastric Tube Placement Knowledge Test:
Time Frame: 3months
|
A knowledge test was created by the researcher in line with the scope and objectives of the theoretical course content of NGS placement prepared in line with the literature (Lynn, P. (2018)).
The knowledge test consists of 20 multiple-choice questions with five options that question the information required for NGS placement.
The lowest score possible from this test is 0 (zero), and the highest is 20.
The distribution of questions in the knowledge test was prepared according to the target behaviors within the subject.
|
3months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
FR.3 Nasogastric Tube Placement Skill Checklist:
Time Frame: 3months
|
It includes the materials to be used in the Nasogastric Tube Placement application and the steps to ensure that the application is carried out correctly.
The checklist prepared by the researcher consists of 51 steps.
Each procedure step will be evaluated as "Correct Application", "Incorrect Application" and "Not Observed" and each will be scored considering the characteristics of the procedure.
|
3months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Bahar Çiftçi, Atatürk University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- Toplantı/Karar Sayısı:8 /3
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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