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.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

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

Breastfeeding Knowledge Questionnaire

Timeframe: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention

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

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

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

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

Trial details

NCT IDNCT07071285

SponsorChina Medical University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-09-30

View on ClinicalTrials.gov More Nursing Education Research trials

Plain-language summary

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.

What they're measuring

Breastfeeding Knowledge Questionnaire

Timeframe: The experimental group and the control group will Baseline (prior to intervention), immediately after intervention, and 4 weeks after intervention

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

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

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

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