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Drug DoseNCT07305233

Pediatric Drug Dose Calculation

A study testing Study Group in people with Drug Dose, run by Ege University at 1 site in Turkey (Türkiye).

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study is a randomized controlled trial that aimed to investigate the effect of a web-supported interactive learning program on the knowledge level of nursing students about pediatric drug dose calculation. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Drug Dose
What is being tested?
Study Group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
108 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Oct 2022to 31 Dec 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Students who had a computer or smartphone and students who volunteered to participate in the study were included in the study

Who cannot join

  • Students who did not have a computer or smartphone and students who did not complete all stages of the study were excluded from the study.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Turkey (Türkiye)1 site, 1 recruiting
  • Ege University

    Izmir, 35100

    Dilek ZENGİN, PhD, zngn.dilek@gmail.com

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Web-Supported Interactive Learning on the Knowledge Level of Nursing Students on Pediatric Drug Dose Calculation: A Randomized Controlled Study

This study is a randomized controlled trial that aimed to investigate the effect of a web-supported interactive learning program on the knowledge level of nursing students about pediatric drug dose calculation.

The study was conducted at one of Turkey's most established nursing faculties, and 108 students participated in the study. Participants were randomly assigned to study (n:54) and control (n:54) groups. The study group received both a traditional lecture and a Web-supported interactive learning application, while the control group was limited to a traditional lecture-based instruction. The "Drug Dose Calculation Knowledge Test", "Perceived Learning Scale", and "Medication Administration Self-Efficacy Scale in Children for Nursing Students" scales were used to collect the data.

Read the detailed description

Purpose and Type of Research This study aimed to investigate the effect of a web-supported interactive learning program on the knowledge level of nursing students about pediatric drug dose calculation. This randomized controlled trial with two parallel groups (pretest and posttest design) was conducted in accordance with the Consolidated Standards of Reporting Trials (CONSORT) checklist.

Population and Sample of the Study This study was conducted at a Nursing Faculty located in Western Turkey. The population of this study consisted of 3rd-year students (n = 346) studying at the Faculty of Nursing for the first time in the first semester of the 2022-2023 academic year. The research sample was determined through a power analysis using the G*Power 3.1.9.2 program under the Repeated Measures ANOVA test to identify the significant difference between the groups before and after the training. For the analysis, with an alpha level of 0.05, an effect size of 0.25, and 80% power, a minimum sample of 98 (49 people per group) was found sufficient. To account for potential data loss in the sample group, a total of 108 students -10% more than the sample number- were included in the study. A simple randomization method was used for sample selection and a randomization list was determined. The participants were assigned to the study and control groups according to the randomization list.

Third-year undergraduate nursing students enrolled in the Diseases and Nursing Care II lecture for the first time in the first semester of the 2022-2023 academic year were invited to participate in this study. Students who had a computer or smartphone and students who volunteered to participate in the study were included in the study. Students who did not have a computer or smartphone and students who did not complete all stages of the study were excluded from the study.

Data Collection and Analysis Third-year nursing students take the Diseases and Nursing Care II lecture in the autumn term. Students do 1 week of laboratory practice after 3 weeks of theoretical course education. In laboratory practice, they receive training on Pediatric Drug Dose Calculation. Before starting the laboratory practice for the project study, a face-to-face meeting was planned before the major courses were attended by all 3rd year students and students were informed about the purpose, goal, and procedures of the study. The students were informed that participation in the study was voluntary and would not affect their academic achievement in any way. The first 108 students who were willing to participate in the study were included in the study and were assigned to the control and study groups according to the randomization list. Data collection for both groups was carried out as follows.

Control Group (n=54) Day 1 The aim, objective, and study steps of the study were verbally explained to participants in a face-to-face meeting. The students were informed that they could withdraw from the study for any reason at any stage of the study and that their participation in the study would not affect their academic achievement. In addition, students' written consent was obtained through the voluntary consent form containing all these statements. The students were placed according to the exam order and were first asked to fill in the "Individual Identification Form". Once all the students completed the form, they were informed about the content and duration of the "Drug Dose Calculation Knowledge Test" pretest, which they then completed within 30 minutes.

Day 2 Face-to-face training was given to the students in this group via a "Pediatric Drug Dose Calculation" PowerPoint presentation. The training was supported with visual materials and active participation of students was ensured with question-answer interactions.

Day 9 One week after the training, the "Drug Dose Calculation Knowledge Test" post-test was applied, with students seated according to their exam order. Students were given 30 minutes to complete the post-test. After completing the post-test, the "Perceived Learning Scale", which enables the student to make a self-assessment on the subject, and the "Medication Administration Self-Efficacy Scale in Children for Nursing Students", which enables the student to make a self-assessment on drug administration, were distributed and the scales were filled in.

Study Group (n=54):

Day 1 The aim, objective, and study steps of the study were verbally explained to participants in a face-to-face meeting. The students were informed that they could withdraw from the study for any reason at any stage of the study and that their participation in the study would not affect their academic achievement. In addition, students' written consent was obtained through the voluntary consent form containing all these statements. The students were placed according to the exam order and were first asked to fill in the 'Individual Identification Form'. Once all the students completed the form, they were informed about the content and duration of the 'Drug Dose Calculation Knowledge Test' pretest, which they then completed within 30 minutes.

Day 2 Face-to-face training was given to the students in this group via a "Pediatric Drug Dose Calculation" PowerPoint presentation. The training was supported with visual materials and active participation of the students was ensured with question-answer interactions. After the verbal training was completed, the students were informed about the use of the interactive learning application created through the Edpuzzle program. Information was given about how to access the application, how to answer the questions in the interactive application, how to use the Edpuzzle application, and how students can see the correct and incorrect applications in the interactive video. Students were also informed that they could access the interactive application at any time, from any location, and as often as they desired.

Day 9 One week after the training, the "Drug Dose Calculation Knowledge Test" post-test was applied, with students seated according to their exam order. Students were given 30 minutes to complete the post-test. After completing the post-test, the "Perceived Learning Scale", which enables the student to make a self-assessment on the subject, and the "Medication Administration Self-Efficacy Scale in Children for Nursing Students", which enables the student to make a self-assessment on drug administration, were distributed and the scales were filled in.

Data Collection Instruments The study data were collected using the 'Individual Identification Form', "Drug Dose Calculation Knowledge Test", "Perceived Learning Scale" and "Medication Adminstration Self-Efficacy Scale in Children for Nursing Students".

Individual Identification Form: The form, developed by the researchers, consisted of 5 questions including age, gender, graduated school, achievement status, and satisfaction with the nursing profession.

Drug Dose Calculations Knowledge Test: It was prepared by the researchers in line with the relevant literature. Each item in the test has a different scoring scheme. The Pediatric Drug Dose Calculations Knowledge Test consists of a total of 17 items including 6 conversion calculations, 3 safe dose range calculations, 1 drug dose calculation, 5 calculations including dry powder volume, 1 body surface area calculation formula, and 1 definition of dry powder volume. Expert opinion was taken for the content validity of the test.

Perceived Learning Scale: The Turkish validity and reliability of the scale was established. Consisting of 9 items, the scale has three factors to measure cognitive, affective, and psychomotor perceived learning. The total score of the scale varies between 9-63 and it takes 3-5 minutes to complete the scale. The Cronbach's Alpha reliability coefficient of the scale is 0.79. Permission was obtained from the authors for the use of the scale.

Medication Administration Self-Efficacy Scale in Children for Nursing Students: The scale aims to determine the self-efficacy levels of nursing students regarding drug administration in children. It consists of 16 items and 2 sub-scales. Total scores range from 16 to 80, with higher scores indicating greater self-efficacy in pediatric drug administration. The Cronbach's alpha coefficient was 0.94for the overall scale, 0.91 for the first drug preparation sub-scale, and 0.87 for the second drug administration sub-scale. Permission was obtained from the authors for the use of the scale.

Pediatric Drug Dose Calculation PowerPoint Presentation: The presentation was prepared by the project team based the relevant and current literature. Pediatric Drug Dose Calculation PowerPoint presentation includes the responsibility of the pediatric nurse in drug administration, how drug dose calculation is performed in pediatrics, determination of the safe dose range of drugs, dry powder volume, conversion calculations and drug calculation examples.

Pediatric Drug Dose Calculation Interactive Application: The interactive application is a video game prepared in line with the relevant literature to include the responsibility of the pediatric nurse in drug administration, how drug dose calculation is performed in pediatrics, determination of the safe dose range of drugs, dry powder volume, conversion calculations and drug calculation examples. The video content was prepared to be the same as the PowerPoint presentation. After the filming was completed by the researchers, the videos were edited by the experienced researcher. During the video shooting, pediatric drug dose calculation was mentioned comprehensively to make students aware of their mistakes and to minimize the risk of dose error. To edit the video content, the video was uploaded to the Edpuzzle program by logging in as an educator. Open-ended and multiple-choice questions that students should answer in the video were embedded in the 'edit' section in the 'Video Preview' section of the Edpuzzle application. A team was created via the Microsoft Teams application for students to access the edited video content. A class was assigned to the team created with Microsoft Teams from Eddpuzzle, which allowed tracking of correct and incorrect responses by students.

Conditions
Drug Dose
Being tested
Study Group
Keywords
Pediatric nursing, drug calculation, ınteractive learning

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Study GroupOther

    The study was conducted with nursing students who were verbally informed about the aim, objectives, and procedures in a face-to-face meeting. They were told that participation was voluntary, could be withdrawn at any time, and would not affect academic performance. Written consent was obtained. On Day 1, students filled in the "Individual Identification Form" and completed the "Drug Dose Calculation Knowledge Test" pretest within 30 minutes. On Day 2, face-to-face training on "Pediatric Drug Dose Calculation" was provided using a PowerPoint presentation supported by visuals and interactive discussions. Students were then introduced to an interactive Edpuzzle application, informed about its use, access, and feedback features, and allowed to use it anytime. On Day 9, one week later, the post-test of the knowledge test was administered, followed by the "Perceived Learning Scale" and "Medication Administration Self-Efficacy Scale in Children for Nursing Students."

Study groups in NCT07305233
Study groupRoleWhat they receive
Control GroupNo interventionControl Group (n=54) Day 1 The aim, objective, and study steps of the study were verbally explained to participants in a face-to-face meeting. The students were informed that they could withdraw from the study for any reason at any stage of the study and that their participation in the study would not affect their academic achievement. In addition, students' written consent was obtained through the voluntary consent form containing all these statements. The students were placed according to the exam order and were first asked to fill in the "Individual Identification Form". Once all the students completed the form, they were informed about the content and duration of the "Drug Dose Calculation Knowledge Test" pretest, which they then completed within 30 minutes. Day 2 Face-to-face training was given to the students in this group via a "Pediatric Drug Dose Calculation" PowerPoint presentation. The training was supported with visual materials and active participation of students was ens
study groupExperimentalStudy Group (n=54): Day 1 The aim, objective, and study steps of the study were verbally explained to participants in a face-to-face meeting. The students were informed that they could withdraw from the study for any reason at any stage of the study and that their participation in the study would not affect their academic achievement. In addition, students' written consent was obtained through the voluntary consent form containing all these statements. The students were placed according to the exam order and were first asked to fill in the 'Individual Identification Form'. Once all the students completed the form, they were informed about the content and duration of the 'Drug Dose Calculation Knowledge Test' pretest, which they then completed within 30 minutes. Day 2 Face-to-face training was given to the students in this group via a "Pediatric Drug Dose Calculation" PowerPoint presentation. The training was supported with visual materials and active participation of the students was
Receives: Other: Study Group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. knowledge level

    Knowledge level of nursing students about pediatric drug dose calculation by using the Drug Dose Calculation Knowledge Test. The Pediatric Drug Dose Calculations Knowledge Test consists of a total of 17 items including 6 conversion calculations, 3 safe dose range calculations, 1 drug dose calculation, 5 calculations including dry powder volume, 1 body surface area calculation formula, and 1 definition of dry powder volume.

    Measured: 9 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Dec 2025
  2. Study start1 Oct 2022
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion31 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Third-year nursing students take the Diseases and Nursing Care II lecture in the autumn term. Students do 1 week of laboratory practice after 3 weeks of theoretical course education. In laboratory practice, they receive training on Pediatric Drug Dose Calculation. Before starting the laboratory practice for the project study, a face-to-face meeting was planned before the major courses were attended by all 3rd year students and students were informed about the purpose, goal, and procedures of the study. The students were informed that participation in the study was voluntary and would not affect their academic achievement in any way. The first 108 students who were willing to participate in the study were included in the study and were assigned to the control and study groups according to the randomization list. Data collection for both groups was carried out as follows.
Masking
Single blind
Who is masked
Participant
Enrolment
108 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07305233
Sponsor's protocol ID
741023
Status last verified
Dec 2025
First submitted
26 Nov 2025
Last updated
26 Dec 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: I have not decided yet.

Questions about this trial

What is this clinical trial studying?

A study testing Study Group in people with Drug Dose, run by Ege University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 26 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Dilek Zengin (+905074575107, zngn.dilek@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

knowledge level (time frame: 9 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Dec 2025; AzTrials last refreshed its copy on 28 Oct 2026.

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