NCT07739472

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
14 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
13 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 14, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

July 28, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 31, 2026

Completed
Last Updated

July 31, 2026

Status Verified

July 1, 2026

Enrollment Period

14 days

First QC Date

July 28, 2026

Last Update Submit

July 28, 2026

Conditions

Keywords

Mobile Application-Supported EducationNursing EducationNursing StudentsClinical Skills TrainingMobile Learning

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

EXPERIMENTAL

Participants 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.

Behavioral: Mobile Application-Supported Nursing Skills EducationBehavioral: Standard Nursing Skills Education

Standard Education Control

ACTIVE COMPARATOR

Participants 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.

Behavioral: Standard Nursing Skills Education

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.

Mobile Application-Supported Education

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.

Mobile Application-Supported EducationStandard Education Control

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Maltepe University, Faculity of Nursing

Istanbul, 38457, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants were randomized in a 1:1 ratio to a mobile application-supported education group or a standard education control group. The intervention group received access to the educational modules for 14 days, while the control group had no access during the initial 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
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.

Locations