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Completed

NCT Number: NCT07739472

Mobile Application-Supported Education in Nursing Students

This randomized controlled study evaluates the effectiveness of a mobile application-supported educational intervention on learning outcomes among first-year undergraduate nursing students. The study focuses on fundamental nursing skills related to oral, local, and parenteral medication administration.

Students who met the eligibility criteria and agreed to participate were randomly assigned to an intervention group or a control group in a 1:1 ratio. All participants first received the standard theoretical instruction and laboratory-based skills training provided as part of the Fundamentals of Nursing course.

Students assigned to the intervention group were then given password-protected access to a mobile application for 14 days. The application included instructional videos and educational content related to oral and local medication administration, subcutaneous and intramuscular injections, blood glucose measurement, blood sampling, and intravenous catheter insertion. The application had separate student and instructor interfaces. During the intervention period, the course instructor monitored students' participation and application completion percentages through the instructor interface. Students in the control group did not have access to the educational modules during this period.

At the end of the two-week intervention, both groups completed a knowledge test and the Student Satisfaction and Self-Confidence in Learning Scale. On the same day, students underwent an Objective Structured Clinical Examination (OSCE) in the nursing skills laboratory. The OSCE was conducted by a second researcher who was blinded to group allocation. For students in the control group, only the OSCE assessment module was activated immediately before the examination; the educational modules remained inaccessible until the initial outcome assessments were completed.

After completion of the randomized comparison and OSCE assessments, access to the mobile application was provided to all participants. Following an additional two-week access period, students' general attitudes toward mobile learning and e-learning were assessed. This final assessment was intended to describe participants' overall attitudes toward digital learning rather than to estimate a randomized between-group intervention effect.

The primary outcomes are nursing knowledge and clinical skills performance. Secondary outcomes include student satisfaction, self-confidence in learning, attitudes toward e-learning, and mobile application usability. The findings are expected to provide evidence regarding the use of mobile learning technologies to support theoretical knowledge and clinical skills development in undergraduate nursing education.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Maltepe University, Faculity of Nursing

Istanbul, 38457, Turkey (Türkiye)

About this study

Mobile technologies may support nursing education by enabling students to review clinical skills repeatedly and independently of time and place. This study was designed to examine whether adding a structured mobile learning resource to standard Fundamentals of Nursing instruction improves students' short-term learning outcomes.

Before randomization, all participants received the same classroom-based theoretical instruction and laboratory skills training. Eligible students were then randomly allocated in a 1:1 ratio to the mobile application-supported education group or the standard education group. Allocation was performed using a computer-generated block randomization sequence. The researcher responsible for the OSCE assessment was not involved in the randomization or intervention process and remained blinded to group allocation.

Students assigned to the intervention group received individual, password-protected access to the mobile application for 14 days. The application contained instructional materials and skill demonstration videos related to oral and local medication administration, subcutaneous and intramuscular injections, blood glucose measurement, blood sampling, and intravenous catheter insertion. Separate student and instructor interfaces were available. Through the instructor interface, the course instructor monitored each participant's access and application completion percentage during the intervention period. Participants were asked to complete at least 50% of the available content.

During the initial randomized comparison period, the control group continued with standard course instruction and did not have access to the educational modules in the mobile application. At the end of the 14-day period, both groups completed the knowledge assessment and the Student Satisfaction and Self-Confidence in Learning Scale before the skills examination.

Clinical skills were evaluated through an Objective Structured Clinical Examination conducted in the nursing skills laboratory. Immediately before each participant in the control group entered the examination, only the OSCE assessment module of the application was activated to allow electronic recording of the skills evaluation. The educational modules remained inaccessible to the control group during the assessment. The OSCE was conducted by the second researcher, who was blinded to group allocation, while the course instructor, who was aware of the group assignments, did not participate in performance scoring.

After the initial knowledge, satisfaction, self-confidence, and OSCE assessments had been completed, the educational content of the mobile application was made available to the control group. Following a two-week access period for the control group, all participants completed the Attitude Toward E-Learning Scale. This assessment was used to describe students' overall attitudes toward mobile and electronic learning after experiencing the application and was not intended to estimate a randomized between-group intervention effect.

Mobile application usability and participant engagement were also evaluated. Student-level completion data obtained from the application were used to document adherence to the mobile learning intervention. The study was conducted as an assessor-blinded randomized controlled educational trial in which the control group was provided with two weeks of access to the mobile application after the initial assessments were completed.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

- Aged 18 years or older. - First-year undergraduate nursing student enrolled in the Fundamentals of Nursing course. - Willing to participate in the study and provide written informed consent. - Possession of a smartphone compatible with the mobile application.

Exclusion criteria

- Previous formal training in oral, local, or parenteral medication administration skills. - Previous clinical or laboratory experience in oral, local, or parenteral medication administration skills. - Failure to meet any of the inclusion criteria.

Treatment and study plan

Mobile Application-Supported Nursing Skills Education

Behavioral

Participants assigned to the intervention group received individual, password-protected access to a mobile application for 14 days in addition to standard theoretical instruction and laboratory skills training. The application included instructional content and skill demonstration videos on oral and local medication administration, subcutaneous and intramuscular injections, blood glucose measurement, blood sampling, and intravenous catheter insertion. Separate student and instructor interfaces were available. The course instructor monitored each participant's application access and completion percentage through the instructor interface. Participants were asked to complete at least 50% of the available content. The control group had no access to the educational modules during the initial 14-day randomized comparison period.

Standard Nursing Skills Education

Behavioral

All participants received the standard theoretical instruction and laboratory-based nursing skills training provided within the Fundamentals of Nursing course. The training covered oral and local medication administration, subcutaneous and intramuscular injections, blood glucose measurement, blood sampling, and intravenous catheter insertion. Participants in the control group received only this standard education during the initial 14-day randomized comparison period and did not have access to the educational modules of the mobile application.

Primary outcomes

  1. Nursing Skills Knowledge Score

    Time frame: At the end of the 14-day intervention period

    Nursing skills knowledge was assessed using a researcher-developed knowledge test covering oral and local medication administration, subcutaneous and intramuscular injections, blood glucose measurement, blood sampling, and intravenous catheter insertion. Each correct response was scored as 1 and each incorrect response as 0. Higher total scores indicate a higher level of knowledge.

  2. Clinical Skills Performance Score

    Time frame: At the end of the 14-day intervention period

    Clinical skills performance was assessed through an Objective Structured Clinical Examination using skill-specific evaluation checklists. Each participant performed selected nursing skills in the nursing skills laboratory. Performance was scored by a researcher who was blinded to group allocation. Higher scores indicate better clinical skills performance.

Sponsors and collaborators

Lead sponsor

Maltepe University

Other

Registry information

Official study title

Effectiveness of a Mobile Application-Supported Educational Intervention on Learning Outcomes in Nursing Students: A Randomized Controlled Trial

Acronym: MU-NS-MOBİLEAP

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 31, 2026
Registry last updated
Jul 31, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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