NCT06889077

Brief Summary

This study is planned as a randomized controlled trial to examine the effects of the use of QR (Quick Response) Code-supported materials prepared for perioperative care by nursing students during clinical practice on the knowledge levels of nursing students and their attitudes towards evidence-based nursing.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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

December 15, 2024

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

March 11, 2025

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 15, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 21, 2025

Completed
Last Updated

March 21, 2025

Status Verified

March 1, 2025

Enrollment Period

3 months

First QC Date

March 11, 2025

Last Update Submit

March 15, 2025

Conditions

Keywords

Clinical PracticeNursing StudentsNursing EducationEvidence Based NursingKnowledge LevelQuick Response Code

Outcome Measures

Primary Outcomes (1)

  • Change from knowledge level in clinical practice

    Educational materials supported by QR codes will enhance students' knowledge of perioperative care in clinical practice. This status will be assessed through a Post-Test measuring knowledge of evidence-based practices in perioperative care. The Post-Test, developed by the researchers, consists of 20 questions, each with four answer options. Each correct answer is worth 5 points, resulting in a possible score range from 0 to 100. A higher score indicates a greater level of knowledge.

    After Using QR Codes in Clinical Practice. An average of 5 months.

Secondary Outcomes (1)

  • Changes in attitude toward evidence-based nursing after clinical practice

    After Using QR Codes in Clinical Practice. An average of 5 months.

Study Arms (2)

QR Code Group

EXPERIMENTAL

Students will receive support in their clinical practice through QR Code-supported perioperative education materials. Students knowledge level and attitudes towards evidence-based nursing will be evaluated after clinical practice.

Other: QR Code Group

Control Group

NO INTERVENTION

Students knowledge level and attitudes towards evidence-based nursing will be evaluated after clinical practice.

Interventions

Students will receive support in their clinical practice through QR Code-supported perioperative education materials.

QR Code Group

Eligibility Criteria

Age18 Years+
Sexall(Gender-based eligibility)
Gender Eligibility DetailsHaving taken a course in surgical diseases nursing
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being a second-year student at Gülhane Nursing Faculty of Health Sciences University
  • Agreeing to participate in the study

You may not qualify if:

  • Not completing any stage of the study
  • Wanting to withdraw from the study
  • Having previously taken the surgical disease nursing course

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Health Sciences Turkiye Gulhane Faculty of Nursing

Ankara, Turkey (Türkiye)

Location

Study Officials

  • Emine Arici Parlak, PhD

    University of Health Sciences Turkiye Gulhane Faculty of Nursing

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

March 11, 2025

First Posted

March 21, 2025

Study Start

December 15, 2024

Primary Completion

March 15, 2025

Study Completion

March 15, 2025

Last Updated

March 21, 2025

Record last verified: 2025-03

Locations