NCT07410013

Brief Summary

This randomized controlled trial aims to evaluate the effect of an ARCS-based escape room educational intervention on nursing students' medication administration knowledge, clinical skills, and learning motivation. Medication administration errors represent a major threat to patient safety, and nursing students must develop safe medication practices early in their education through effective and engaging instructional approaches. The study will be conducted with first-year undergraduate nursing students enrolled in a Fundamentals of Nursing course at a public university. Participants will be randomly assigned to either an intervention group or a control group. Both groups will receive standard theoretical instruction and laboratory-based training on medication administration. In addition, the intervention group will participate in an ARCS-based escape room activity designed to reinforce medication administration competencies. The escape room intervention will be structured according to Keller's ARCS Motivation Model (Attention, Relevance, Confidence, Satisfaction) and will include scenario-based learning stations focusing on oral medication administration and parenteral medication administration operationalized as subcutaneous and intravenous routes. Each station will require students to apply medication safety principles, clinical decision-making, and procedural skills within a time-limited, team-based game environment. Primary outcomes will include medication administration knowledge and clinical skill performance assessed using a structured knowledge test and objective structured clinical examination (OSCE). Learning motivation will be evaluated as a secondary outcome using a validated motivation scale based on the ARCS model. Assessments will be conducted at baseline and after completion of the educational intervention. The findings of this study are expected to provide evidence regarding the effectiveness of ARCS-based escape room education as an innovative, student-centered instructional strategy for improving medication administration competencies and learning motivation among nursing students.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
110

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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

February 1, 2026

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

February 7, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 13, 2026

Completed
16 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

February 19, 2026

Status Verified

February 1, 2026

Enrollment Period

28 days

First QC Date

February 7, 2026

Last Update Submit

February 18, 2026

Conditions

Keywords

Nursing studentsMedication administrationEscape room educationARCS motivation modelRandomized controlled trial

Outcome Measures

Primary Outcomes (3)

  • Intravenous Catheter Insertion Skill Score

    Medication administration skill related to intravenous catheter insertion will be assessed using a structured observational checklist (score range: 0-42). Each procedural step is scored dichotomously (0 = not performed/incorrect; 1 = correctly performed). Higher scores indicate better clinical performance.

    From baseline to immediately after the intervention

  • Intravenous Fluid Therapy Initiation Skill Score

    Intravenous fluid therapy initiation skills will be assessed using a structured observational checklist (score range: 0-50). Each procedural step is scored dichotomously (0 = not performed/incorrect; 1 = correctly performed). Higher scores indicate better clinical performance.

    From baseline to immediately after the intervention

  • Intravenous Bolus Medication Administration Skill Score

    Intravenous bolus medication administration via IV catheter will be assessed using a structured observational checklist (score range: 0-34). Each procedural step is scored dichotomously (0 = not performed/incorrect; 1 = correctly performed). Higher scores indicate better clinical performance.

    From baseline to immediately after the intervention

Secondary Outcomes (1)

  • Motivation Toward Instructional Materials

    From baseline to immediately after the intervention

Study Arms (2)

ARCS-Based Escape Room Education

EXPERIMENTAL

Nursing students receive an ARCS-based escape room educational intervention designed to improve medication administration skills.

Behavioral: ARCS-Based Escape Room Education

Standard Education

NO INTERVENTION

Nursing students receive standard medication administration education according to the existing curriculum.

Interventions

A simulation-based educational intervention structured according to the ARCS motivation model and delivered through an escape room format to enhance medication administration skills.

ARCS-Based Escape Room Education

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Being a first-year student Taking the Basic Principles and Practices in Nursing course for the first time Voluntarily participating in the study..

You may not qualify if:

  • Being a graduate of a health vocational high school Not participating in theoretical and laboratory training Not completing data collection forms; and Wanting to withdraw from the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Gözde ÖZARAS ÖZ, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: This study was designed as a pre-test-post-test, randomized controlled trial with a control group.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Dr. Lecturer

Study Record Dates

First Submitted

February 7, 2026

First Posted

February 13, 2026

Study Start

February 1, 2026

Primary Completion

March 1, 2026

Study Completion

April 1, 2026

Last Updated

February 19, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared outside the research team due to ethical considerations, institutional policies, and the nature of the educational intervention involving a limited student population.