NCT07525700

Brief Summary

This study aimed to explore the impact of electronic picture books combined with RPG on breastfeeding learning outcomes among nursing students. The study participants were third-year nursing students from a university in central Taiwan. A randomized controlled design was used, with the experimental group receiving electronic picture books combined with RPG, while the control group received traditional face-to-face instruction. Changes in students' breastfeeding knowledge, learning motivation, self-efficacy, and cognitive load were assessed. The expected results can provide a reference for innovative teaching models in nursing education and promote the future clinical application of breastfeeding.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
3mo left

Started Sep 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 7, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
6 months until next milestone

Study Start

First participant enrolled

September 30, 2026

Expected
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

April 13, 2026

Status Verified

April 1, 2026

Enrollment Period

2 months

First QC Date

April 7, 2026

Last Update Submit

April 7, 2026

Conditions

Keywords

nursing educationlearning motivationBreastfeeding EducationNursing Studentselectronic picture booksRPG

Outcome Measures

Primary Outcomes (4)

  • Breastfeeding Knowledge Questionnaire

    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

    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

  • ARCS-Based Learning Motivation Scale

    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

  • Cognitive Load Scale

    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

Study Arms (2)

face-to-face teaching

ACTIVE COMPARATOR

face-to-face teaching of breastfeeding

Behavioral: face-to-face teaching

Electronic picture books and Online RPG interactive adventure game

EXPERIMENTAL

Integration of online RPG interactive adventure games with an electronic picture books learning mode for the instruction of breastfeeding.

Behavioral: Electronic picture books and Online RPG interactive adventure game

Interventions

face-to-face teaching of breastfeeding

face-to-face teaching

Integration of online RPG interactive adventure games with an electronic picture books learning mode for the instruction of breastfeeding.

Electronic picture books and Online RPG interactive adventure game

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: The study design will adopt a randomized controlled trial with repeated measures. A 60-minute intervention has been developed.Block randomization stratified by gender will be used, and eligible participants will be randomly assigned to either the experimental or control group in a 1:1 ratio using Random Allocation Software.Research assistants will code group assignments ("Group 1" and "Group 2") according to the randomization list, place the assignments into opaque sealed envelopes, and arrange them sequentially.On the day of the study, envelopes will be distributed in the order participants submit their consent forms. Participants will open the envelope themselves to learn their group assignment.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

April 7, 2026

First Posted

April 13, 2026

Study Start (Estimated)

September 30, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

April 13, 2026

Record last verified: 2026-04