NCT07700290

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

87
On Track

Trial Health Score

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

Enrollment
106

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Completed
4 days until next milestone

First Submitted

Initial submission to the registry

July 5, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 14, 2026

Completed
Last Updated

July 14, 2026

Status Verified

July 1, 2026

Enrollment Period

6 months

First QC Date

July 5, 2026

Last Update Submit

July 11, 2026

Conditions

Keywords

chatbotArtificial IntelligenceNursing StudentsPediatric NursingMedication AdministrationSelf-EfficacyDigital Health Education

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

EXPERIMENTAL

Participants 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.

Behavioral: Chatbot-supported training

Control group

NO INTERVENTION

Participants 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.

Experimental group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Two-group parallel pre-test-post-test randomized controlled trial
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

Locations