Artificial Intelligence-Assisted Learning for Nursing Drug Calculation

March 27, 2026 updated by: Mohamed Fakhry Ahmed Salem, Alexandria University

Adaptive AI-Based Mobile Simulation for Drug Calculation Competency in Nurses: A Mixed-Methods RCT

The purpose of this study is to evaluate how an Artificial Intelligence -assisted learning platform affects nurses' ability to calculate medication dosages accurately. Drug calculation is a critical skill in nursing, and errors can significantly impact patient safety.

While traditional teaching methods are standard, they may not provide the personalized feedback needed for such a high-stakes task. This study compares two groups of nurses: one group using an Artificial Intelligence-driven software that provides interactive scenarios and real-time guidance, and another group receiving traditional classroom instruction.

The researchers aim to determine whether the AI approach leads to:

Improved theoretical knowledge of drug calculations. Enhanced clinical decision-making during medication administration. Increased nurses' confidence (self-efficacy) in performing these tasks in real clinical settings.

In addition, a qualitative component conducted using focus group discussions to explore participants' acceptance, perceived usefulness, usability, and overall perceptions of the AI-assisted learning platform. This qualitative inquiry provides a deeper insight into nurses' experiences, attitudes toward AI integration in education, and their opinions regarding the effectiveness of the teaching and learning strategies used within the platform.

Study Overview

Detailed Description

Medication administration errors are a significant challenge in nursing practice, particularly in high-acuity environments such as cardiovascular and critical care units. This study evaluates the effectiveness of an Artificial Intelligence-driven educational intervention designed to bridge the gap between theoretical knowledge and clinical application in drug calculations.

Study Design

This study employed a mixed-methods design comprising a quasi-experimental pretest-posttest approach with a control group, complemented by a qualitative focus group component. Participants were allocated to either an experimental group receiving Artificial Intelligence-assisted learning or a control group receiving traditional instruction

The Intervention (ٍStudy Group)

Participants in the experimental group used Artificial Intelligence-assisted learning software designed to enhance their educational experience through several advanced features. The software provides Adaptive Learning Paths, which adjust calculation complexity in accordance with the nurse's performance. Additionally, it offers Real-Time Feedback, ensuring immediate corrections and step-by-step guidance for complex drug dosing. Lastly, the software incorporates Artificial Intelligence-based Clinical Simulations that create high-pressure clinical decision-making scenarios for learners.

The Control Group

Participants in the control group received traditional teaching methods that encompassed standard lectures and paper-based practice sessions specifically aimed at drug calculation. This approach covered the same core curriculum as the experimental group but did not incorporate any Artificial Intelligence assistance.

The study evaluated three key areas before and after the intervention:

Nursing Knowledge, assessed using a standardized drug calculation examination.

Clinical Decision-Making, measured with a validated nursing decision-making scale.

Self-Efficacy, evaluated through a standardized self-efficacy scale to assess confidence in clinical calculations.

Data were analyzed using the Statistical Package for the Social Sciences to compare the mean scores between the experimental and control groups.

Qualitative Component (Focus Group Study)

To complement the quantitative findings, a qualitative focus group study was conducted with participants from the experimental group. The aim was to explore nurses' acceptance of the Artificial Intelligence platform, perceived usefulness, usability, visibility of learning progress, and overall opinions regarding the Artificial Intelligence-assisted teaching strategies.

Focus group discussions were audio-recorded, transcribed, and analyzed using thematic analysis to identify recurring patterns and themes related to user experience, perceived educational value, and readiness to integrate AI-based learning into clinical education. This qualitative component provided deeper insight into participants' attitudes toward AI integration in nursing education and enriched the interpretation of the quantitative outcomes.

Study Type

Interventional

Enrollment (Actual)

56

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alexandria Governorate
      • Alexandria, Alexandria Governorate, Egypt, 2500
        • Faculty of Nursing, Alexandria University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

Nurses working in multiple clinical settings, including medical-surgical, cardiovascular, or critical care units..etc.

Nurses are responsible for medication administration and drug dosage calculations as part of their daily clinical duties.

Willingness to participate in the Artificial Intelligence-assisted learning program and sign the informed consent.

Exclusion Criteria:

Nurses who had recently received specific training in drug-calculation or had any prior exposure to AI-based educational tools (within the last 6 months)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Artificial Intelligence-Assisted Learning Group
Use an Artificial Intelligence-assisted platform providing scenario-based learning and real-time feedback for drug calculations.
An innovative Artificial Intelligence software enhances nursing accuracy in drug calculations and clinical reasoning through scenario-based learning, providing real-time feedback and adaptive learning paths.
Experimental: Traditional Learning Group
Participants receive the standard curriculum through traditional lectures and paper-based practice sessions.
Standard classroom-based instruction consists of theoretical lectures and paper-based practice focusing on medication dosage calculations.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nurses' Knowledge of Drug Calculation
Time Frame: Baseline (Pre-test) and 2 weeks post-intervention (Post-test)

A 16-item assessment tool designed to evaluate the theoretical and practical knowledge of nurses regarding drug calculation principles (e.g., unit conversions, flow rate, and dose calculations). Each correct answer is scored "1" and each incorrect answer is scored "0".

Scale Range: The total score ranges from a minimum of 0 to a maximum of 16.

Interpretation: Higher scores indicate a better outcome (greater mastery of calculation principles).

High (13-16): Competent level (> 80%).

Moderate (10-12): Acceptable but incomplete knowledge (60%-80%).

Low (0-9): Deficient understanding (< 60%).

Baseline (Pre-test) and 2 weeks post-intervention (Post-test)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nurses' Drug Calculation Decision-Making Scale
Time Frame: Baseline (Pre-test) and 2 weeks post-intervention (Post-test)

This scale is an 8-item self-report tool designed to assess the clinical judgment and confidence of nurses regarding medication dosage calculations. Each item is rated on a 5-point Likert scale ranging from 1 (Strongly Disagree) to 5 (Strongly Agree).

Minimum and Maximum Values: The total score ranges from a minimum of 8 to a maximum of 40.

Interpretation: Higher scores indicate a better outcome (greater clinical competence and safer decision-making).

High (30-40): High competence.

Moderate (19-29): Moderate ability; requires supervision.

Low (8-18): Poor confidence and judgment.

Baseline (Pre-test) and 2 weeks post-intervention (Post-test)
General Self-Efficacy Scale
Time Frame: Baseline (Pre-test) and 2 weeks post-intervention (Post-test)

Description: A 10-item psychometric scale used to assess nurses' perceived confidence and self-belief in their ability to perform drug calculations and clinical tasks effectively under various conditions. Each item is scored on a 4-point Likert scale: 1 (Not at all true), 2 (Hardly true), 3 (Moderately true), and 4 (Exactly true).

Scale Range: The total score ranges from a minimum of 10 to a maximum of 40.

Interpretation: Higher scores indicate a better outcome (stronger perceived competence and higher self-efficacy).

High (31-40): Strong perceived competence and self-belief.

Moderate (21-30): Moderate confidence in managing demands.

Low (10-20): Low belief in ability to cope with challenges.

Baseline (Pre-test) and 2 weeks post-intervention (Post-test)
Nurses' Perception and Satisfaction with Artificial Intelligence-Assisted Learning (Qualitative)
Time Frame: 2 weeks after the completion of the AI-assisted training

Description: Assessment of participants' acceptance, perceived usefulness, usability, and satisfaction with the Artificial Intelligence-assisted learning platform. Data will be collected through focus group discussions.

Method of Analysis: Results will be analyzed using Thematic Analysis to identify recurring patterns and themes.

Unit of Measure: This is a qualitative outcome; results will be reported as narrative themes (for example: "Improved Calculation Confidence" or "User Interface Satisfaction").

2 weeks after the completion of the AI-assisted training

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 22, 2025

Primary Completion (Actual)

December 30, 2025

Study Completion (Actual)

December 30, 2025

Study Registration Dates

First Submitted

February 18, 2026

First Submitted That Met QC Criteria

February 28, 2026

First Posted (Actual)

March 4, 2026

Study Record Updates

Last Update Posted (Actual)

April 1, 2026

Last Update Submitted That Met QC Criteria

March 27, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared to protect the privacy and confidentiality of the participating nurses

Study Data/Documents

  1. Study Protocol
    Information comments: Available upon request from the Principal Investigator for legitimate research purposes

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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