Strengthening Numerical Skills and Medication Calculation Abilities of Nursing Students

December 5, 2025 updated by: Beratiye Oner, Lokman Hekim University

Strengthening Numerical Skills and Medication Calculation Abilities of Nursing Students Through Peer Education: A Randomized Controlled Trial

This experimental study aims to evaluate the effect of peer-assisted education on nursing students' numerical and drug calculation skills. A randomized controlled pretest-posttest design will be conducted with 55 first-year nursing students (27 in the experimental group and 28 in the control group). The experimental group will participate in a three-week peer education program focusing on numerical problem-solving and medication dosage calculations, led by trained mentor students.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

55

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

    • Ankara
      • Çankaya, Ankara, Turkey (Türkiye), 06510
        • Lokman Hekim 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:

  • Students who were registered for the Fundamentals of Nursing course for the first time
  • Students who agreed to participate in the research voluntarily

Exclusion Criteria:

  • Students who graduated from a Health Vocational High School
  • Students who had previous training in the health field
  • Students who had previously taken a Fundamentals of Nursing course
  • Students diagnosed with a psychiatric illness
  • Students who were regularly taking psychiatric medications
  • Students who did not attend the theoretical sessions of the course

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention Group
Peer-supported medication calculation training program
The intervention consisted of a peer-supported education program on medication dosage calculation, implemented over three weeks with five 60-minute sessions. In Week 1, four mentor students-senior nursing students with prior training in medication calculations and a GPA above 3.0-received refresher instruction from the course instructor. The training covered decimals, percentages, unit conversions, weight-based and non-weight-based dose calculations, and infusion pump adjustments, followed by sample problem-solving activities. The intervention group was divided into four subgroups, each consisting of 7-8 students, and each was assigned a consistent mentor. Each session included 30 minutes of individual and peer problem-solving followed by 30 minutes of guided mentoring. The course instructor provided supervision and feedback throughout the sessions. During Weeks 2 and 3, students practiced numerical and medication dosage calculations through peer-supported exercises.
No Intervention: Control Group
Participants who received traditional lecture-based instruction

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Medication Calculation Ability
Time Frame: They were evaluated before the intervention and after 3 weeks of intervention.

Medication Calculation Ability Assessment Form (Pre-Test, Post-Test): The pre-test consisted of eight questions. The posttest consisted of twenty questions, including additional questions similar to those in the pretest. The questions covered the following categories:

  • Dosage calculation for solid and liquid oral medications (3 questions in the pretest, 8 questions in the posttest),
  • Dosage calculation for injections (3 questions in the pretest, 7 questions in the posttest),
  • Calculation of percentage solutions and intravenous fluids (2 questions in the pretest, 5 questions in the posttest).

Each correct answer was scored; the participants' correct answers were averaged to convert the score into a percentage. Thus, a medication calculation skill score ranging from 0% to 100% was obtained for each participant.

They were evaluated before the intervention and after 3 weeks of intervention.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Numerical Skills
Time Frame: They were evaluated both before and after the 3-week intervention.
Numerical Skills Assessment Form (Pre-Test, Post-Test): The pre-test consisted of five questions. The post-test consisted of 10 questions, including additional questions similar to those in the pre-test. The questions covered basic numerical skills, including addition, subtraction, multiplication, division, fractions, decimals, percentage calculations, and unit conversions. Each correct answer was scored, and the percentage score was converted by averaging the number of correct answers. Thus, a numerical skill score ranging from 0% to 100% was obtained for each participant.
They were evaluated both before and after the 3-week intervention.

Collaborators and Investigators

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

Investigators

  • Study Director: Beratiye Oner, Lokman Hekim University

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)

May 15, 2024

Primary Completion (Actual)

June 15, 2024

Study Completion (Actual)

June 20, 2024

Study Registration Dates

First Submitted

November 25, 2025

First Submitted That Met QC Criteria

December 5, 2025

First Posted (Estimated)

December 9, 2025

Study Record Updates

Last Update Posted (Estimated)

December 9, 2025

Last Update Submitted That Met QC Criteria

December 5, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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