- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07525700
The Effects of Combining Electronic Picture Books With RPG-Based Gamified Learning on Nursing Students' Motivation and Learning Outcomes in Breastfeeding Education
Study Overview
Status
Detailed Description
Breastfeeding is widely considered to be the best source of nutrition for infants, helping to reduce infant morbidity and mortality, reduce the risk of infection and chronic diseases, and promote intellectual development. However, in current nursing education, how to effectively improve students' knowledge and skills of breastfeeding has yet to be developed. Common traditional face-to-face courses are limited by time and venue, which requires students to re-adapt and learn when entering the clinical internship stage, affecting learning efficiency and clinical application.
This study adopts a randomized controlled experimental design and is expected to recruit 100 third-year nursing students from a university in central Taiwan, divided into an experimental group and a control group. The experimental group studied with electronic picture books combined with RPG on breastfeeding learning, and the control group took a traditional face-to-face course. Data were collected through a structured questionnaire, and changes in breastfeeding knowledge, learning motivation, self-efficacy, and cognitive load were assessed analyzed using descriptive and inferential statistics. The expected results showed that the interactive e-book not only significantly improved students' learning outcomes, but also helped overcome gender restrictions, enhance learning motivation, promote future clinical promotion of breastfeeding, and serve as an important reference for innovative nursing education models.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ting-Shan Chang
- Phone Number: 7116 +886422053366
- Email: tingshan@mail.cmu.edu.tw
Study Contact Backup
- Name: Ya-Ling Tzeng
- Phone Number: 7112 +886422053366
- Email: tyaling@mail.cmu.edu.tw
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- It is expected to include 100 people.
- A third-year nursing student.
- Studying obstetrics and gynecology nursing this semester.
- Agree to participate in this study and sign the research consent form.
Exclusion Criteria:
- Students who are planning to take a leave of absence at the time of data collection.
- Students who have not taken obstetrics and gynecology nursing this semester or have taken it in the past.
- Students who are unable to use 3C products.
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 |
|---|---|
|
Active Comparator: face-to-face teaching
face-to-face teaching of breastfeeding
|
face-to-face teaching of breastfeeding
|
|
Experimental: Electronic picture books and Online RPG interactive adventure game
Integration of online RPG interactive adventure games with an electronic picture books learning mode for the instruction of breastfeeding.
|
Integration of online RPG interactive adventure games with an electronic picture books learning mode for the instruction of breastfeeding.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ARCS-Based Learning Motivation Scale
Time Frame: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
The scale assesses learners' motivation toward the educational materials across four dimensions: Attention (12 items), Relevance (9 items), Confidence (9 items), and Satisfaction (6 items), for a total of 36 items.
Responses are rated on a 5-point Likert scale, ranging from 5 ("Strongly Agree") to 1 ("Strongly Disagree").
The total score ranges from 36 to 180 points, with higher scores indicating stronger learning motivation.
|
The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
|
Breastfeeding Knowledge Questionnaire
Time Frame: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
This questionnaire consists of 10 multiple-choice questions.
Each correct answer is scored 10 points, and each incorrect answer is scored 0 points, yielding a total score range of 0-100.
The questions were self-developed in the form of clinical scenario-based multiple-choice items, focusing on the benefits of breastfeeding, breastfeeding positions, breast milk storage methods, breast milk expression (hand expression), and nursing interventions to maintain milk supply.
|
The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
|
Breastfeeding Self-Efficacy Scale
Time Frame: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
Breastfeeding self-efficacy was evaluated using a 10-item Breastfeeding Self-Efficacy Scale.
Each item is rated on a 4-point Likert scale, where 1 = not at all capable and 4 = expert level.
The total score ranges from 10 to 40, with higher scores indicating greater self-efficacy in performing breastfeeding self-efficacy .
|
The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
|
Cognitive Load Scale
Time Frame: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
The cognitive load of learners taking electronic picture books and RPGs or face-to-face courses was assessed using an 8-item cognitive load scale.
All items were rated on a 1-point Likert scale, ranging from 5 ("strongly agree") to 1 ("strongly disagree").
The total score ranged from 8 to 40, with higher scores indicating stronger cognitive load.
|
The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
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
Keywords
Other Study ID Numbers
- CMUH115-REC1-069
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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