Effect of a Chatbot on Nursing Students' Self-Efficacy in Pediatric Medication Administration
CHATPED
Effect of a Chatbot-Supported Clinical Training on Nursing Students' Self-Efficacy in Pediatric Medication Administration: A Randomized Controlled Trial
1 other identifier
interventional
106
1 country
1
Brief Summary
This study looked at whether a chatbot can help nursing students feel more confident about giving medicines to children. Giving medicines to children is difficult because doses depend on the child's weight, and mistakes can be harmful. Third-year nursing students starting their pediatric clinical placement took part. They were divided by chance into two groups. Both groups received the usual training. One group also used a chatbot that helped with medicine dose calculations and answered questions about giving medicines to children, based on a trusted nursing textbook. The other group used only the usual references. Students' confidence in giving medicines to children was measured with a questionnaire before and after the placement. The study compared how much each group's confidence changed to see whether the chatbot added a benefit beyond the usual training.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2026
CompletedFirst Submitted
Initial submission to the registry
July 5, 2026
CompletedFirst Posted
Study publicly available on registry
July 14, 2026
CompletedJuly 14, 2026
July 1, 2026
6 months
July 5, 2026
July 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Self-efficacy in pediatric medication administration
Self-efficacy measured with the Medication Administration Self-Efficacy Scale in Children for Nursing Students (MASSCNS), a 16-item, 5-point Likert scale with total scores ranging from 16 to 80. Higher scores indicate greater self-efficacy. Change from pre-test to post-test was compared between groups.
Baseline (before the pediatric clinical placement) and post-intervention (after completion of the placement, approximately at the end of the clinical rotation). Baseline (Day 1) and post-intervention (Week 8)
Study Arms (2)
Experimental group
EXPERIMENTALParticipants received the routine curriculum and additionally used a web-based chatbot (a dose calculator and a book-based question-answer assistant) before and during the pediatric clinical placement.
Control group
NO INTERVENTIONParticipants received the routine curriculum and accessed standard clinical references only, without the chatbot.
Interventions
A web-based chatbot accessible via mobile and desktop browsers, containing two modules: an advanced dose calculator that computes required drug amount and volume from the child's weight, prescribed dose, and drug concentration; and a question-answer assistant that responds to pediatric medication questions using content drawn solely from a validated pediatric nursing reference textbook.
Eligibility Criteria
You may qualify if:
- Third-year nursing student
- Entering the pediatric (child health and diseases) clinical placement for the first time
- Owning a smartphone or computer
- Providing voluntary informed consent to participate
You may not qualify if:
- Previous completion of a pediatric clinical placement
- Prior participation in a similar educational intervention
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Üsküdar Univercity
Istanbul, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
July 5, 2026
First Posted
July 14, 2026
Study Start
January 1, 2026
Primary Completion
July 1, 2026
Study Completion
July 1, 2026
Last Updated
July 14, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share