Mobile Application-Supported Education in Nursing Students
MU-NS-MOBİLEAP
Effectiveness of a Mobile Application-Supported Educational Intervention on Learning Outcomes in Nursing Students: A Randomized Controlled Trial
1 other identifier
interventional
80
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
1 active site
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
March 18, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 14, 2026
CompletedFirst Submitted
Initial submission to the registry
July 28, 2026
CompletedFirst Posted
Study publicly available on registry
July 31, 2026
CompletedJuly 31, 2026
July 1, 2026
14 days
July 28, 2026
July 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Nursing Skills Knowledge Score
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.
At the end of the 14-day intervention period
Clinical Skills Performance Score
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.
At the end of the 14-day intervention period
Study Arms (2)
Mobile Application-Supported Education
EXPERIMENTALParticipants in this arm received standard theoretical instruction and laboratory skills training, followed by individual, password-protected access to the mobile application for 14 days. The application included educational content and skill demonstration videos related to oral and local medication administration, subcutaneous and intramuscular injections, blood glucose measurement, blood sampling, and intravenous catheter insertion. Application participation and completion percentages were monitored through the instructor interface.
Standard Education Control
ACTIVE COMPARATORParticipants in this arm received the same standard theoretical instruction and laboratory skills training but did not have access to the educational modules of the mobile application during the initial 14-day randomized comparison period. After completion of the knowledge, satisfaction, self-confidence, and OSCE assessments, the control group received access to the mobile application for two weeks. For the OSCE, only the assessment module was activated immediately before the examination, while the educational modules remained inaccessible until the initial assessments were completed.
Interventions
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.
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.
Eligibility Criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Maltepe University, Faculity of Nursing
Istanbul, 38457, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
July 28, 2026
First Posted
July 31, 2026
Study Start
March 18, 2026
Primary Completion
April 1, 2026
Study Completion
April 14, 2026
Last Updated
July 31, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared because the informed consent process did not include permission for sharing individual-level data with external researchers. Study data will be anonymized, securely stored, and accessed only by the research team.