- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07349862
Flipped Learning in Nursing Education
January 16, 2026 updated by: Dilek Erden, Namik Kemal University
THE IMPACT OF CANCER SCREENING TRAINING, CONDUCTED USING A CHATGPT-SUPPORTED FLIPPED LEARNING MODEL, ON NURSING STUDENTS' ACADEMIC KNOWLEDGE, LEARNING MOTIVATION, AND CLASSROOM ENGAGEMENT
This study aims to examine the effects of cancer screening training, conducted using a ChatGPT-based flipped learning model, on knowledge, learning motivation, and class participation.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Detailed Description
Methods: A randomized controlled trial was conducted with 46 intervention and 46 control groups.
In the study, a training program based on traditional flipped learning and a ChatGPT-based flipped learning model for cancer screenings is applied.
Data will be collected using the Knowledge Form, Cancer Screening Knowledge Scale, Higher Education Learning Motivation Scale, and Class Participation Scale.
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
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
-
-
Suleymanpasa
-
Tekirdağ, Suleymanpasa, Turkey (Türkiye), 59030
- Tekirdag Namık Kemal 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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Students who have taken courses in fundamentals of nursing, internal medicine nursing, physiology, pathology, and computer science, but have not taken a course in oncology nursing,
- Third-year students,
- Those who have voluntarily agreed to participate in the study.
Exclusion Criteria:
- Students who were not third-year students,
- Those who had not taken one of the following courses: fundamentals of nursing, internal medicine nursing, physiology, pathology, computer science, oncology nursing,
- Those who did not volunteer to participate in the research were excluded from the study.
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
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group- ChatGPT Flipped Learning
ChatGPT-Based Flıpped Learnıng Model
|
Training group based on ChatGPT-based flipped learning model
|
|
Placebo Comparator: Control Group- Traditioanl Flipped Learning
Traditional Flıpped Learnıng Model
|
Training group based on traditional flipped learning model
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cancer Screening Knowledge Scale
Time Frame: 4 weeks
|
This scale consists of 25 items and 3 sub-dimensions.
The sub-dimensions are not specifically named.
The first sub-dimension contains 10 items (items 8, 17-23, 25, 28), the second sub-dimension contains 9 items (items 4, 5, 7, 10, 12, 13, 15, 16, 27), and the third sub-dimension contains 6 items (items 1-3, 9, 11, 24).
The scale is a three-point rating scale.
The scale is answered on a scale of 1 to 3, with "1: True, 2: False, 3: I don't know".
When calculating the scale score, "True" answers are worth 1 point, and "False" and "I don't know" answers are worth 0 points.
The lowest possible score on the scale is 0, and the highest is 25.
When calculating the scale score, the three items with negative connotations (Items 2, 11, 24) should be reverse-coded.
The order of the items on the scale is not important; researchers may use a mixed order.
There is no cutoff point for the scale score.
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Learning Motivation Scale in Higher Education
Time Frame: 4 weeks
|
The scale consisting of 23 items on a 3-point Likert scale, participants are given scores of Disagree (1), Don't Know (2), and Agree (3) for each question in the Learning Motivation Scale in Higher Education.
The lowest possible score is 23 and the highest is 69.
In the reliability studies of the scale, the Cronbach alpha coefficient of the learning objectives sub-dimension was calculated as 0.83, the avoidance objectives sub-dimension as 0.87, and the approach objectives sub-dimension as 0.82.
|
4 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Classroom Engagement Scale
Time Frame: 4 weeks
|
The scale consisting of 15 items and 3 sub-dimensions on a 5-point Likert scale, participants are given scores for each question on a scale of 1 (Not Appropriate at all), 2 (Not Appropriate), 3 (Somewhat Appropriate), 4 (Appropriate), and 5 (Completely Appropriate).
The scale includes sub-dimensions of Cognitive participation, Emotional participation, and Behavioral participation.
In reliability studies of the scale, the Alpha value was found to be 0.93.
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: DİLEK ERDEN, Namik Kemal University
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, 2025
Primary Completion (Estimated)
January 30, 2026
Study Completion (Estimated)
February 15, 2026
Study Registration Dates
First Submitted
December 22, 2025
First Submitted That Met QC Criteria
January 16, 2026
First Posted (Actual)
January 20, 2026
Study Record Updates
Last Update Posted (Actual)
January 20, 2026
Last Update Submitted That Met QC Criteria
January 16, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- DERDEN-4
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
I can share it with researchers who request it for reasonable reasons.
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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