Applying Interactive E-books on Breastfeeding to Enhance Nursing Students' Learning (NCT07071285) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Applying Interactive E-books on Breastfeeding to Enhance Nursing Students' Learning
Taiwan100 participantsStarted 2025-09-19
Plain-language summary
This study aims to explore the impact of interactive breastfeeding e-books on nursing students' breastfeeding learning outcomes. The subjects are third-year nursing students from a university in central Taiwan. A randomized controlled design will be adopted. The experimental group will use interactive breastfeeding e-books for learning, while the control group will use traditional face-to-face courses to evaluate the changes in students' breastfeeding knowledge, skills, and learning motivation. The expected results can provide a reference for innovative teaching models in nursing education and promote the future clinical promotion of breastfeeding.
Who can participate
Age range
20 Years – 30 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. It is expected to include 100 people.
. Age 20 to 30 years old.
. 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 have not taken obstetrics and gynecology nursing this semester or have taken it in the past.
.Students who are unable to use 3C products.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial focuses on nursing students learning breastfeeding techniques through interactive e-books rather than testing a medical treatment — so is this study actually relevant to my own care as a patient, or is it purely about training future nurses?
2Since the trial is measuring things like breastfeeding knowledge and self-efficacy in nursing students, could the nurses or midwives on my care team have been trained using similar e-learning tools, and does that affect the quality of breastfeeding support I might receive?
3The study is listed as active but no longer recruiting — does that mean results may be available soon, and is there anything your team has already learned from this type of educational research that could improve the breastfeeding guidance I get during my care?
4Since this trial measures critical thinking and motivation in nursing students rather than patient health outcomes, are there other studies you'd recommend I look at that directly evaluate breastfeeding support interventions for patients like me?
5Given that this is an education research study with no listed phase, meaning it's not testing a drug or device on patients, can you help me understand what kind of trials or resources would actually be most relevant to my personal breastfeeding goals or challenges?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Breastfeeding Knowledge Questionnaire
Timeframe: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
2
Breastfeeding Skills Assessment Scale
Timeframe: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
3
Breastfeeding Self-Efficacy Scale
Timeframe: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
4
ARCS-Based Learning Motivation Scale
Timeframe: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention
5
Critical Thinking Disposition Scale
Timeframe: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention