NCT07266870

Brief Summary

CORE is an assessment tool that uses written scenarios designed to address problems that students may encounter in real clinical settings. These scenarios are presented at different stations. It enables educators to conduct more objective evaluations during the learning process, contributing to effective learning by providing students with immediate feedback. This research will examine the effect of CORE on nursing students' knowledge and attitudes regarding pain assessment. The study will be conducted using a randomised controlled experimental design. The study population will consist of senior nursing students taking the Nursing Professional Practice II course in the spring semester of the 2025/26 academic year at a nursing department in the Central Anatolia region of Turkey (n = 100). The sample for the study will consist of students who agree to participate in the research. Students will be randomized into intervention and control groups based on their pre-test knowledge scores. Research data will be collected using the "Personal Information Form" "Pain Knowledge Test", "Nursing Students' Attitudes Scale Toward Pain Assessment" and "CORE Satisfaction Form". Approval from the ethical committee has been obtained for the research to be conducted, and written permission has been requested from the institution in which the research will take place. Before starting the research, students will be informed about it and asked to provide written informed consent. Students in the intervention group will perform the CORE application on tablets using case scenarios prepared for pain assessment in the Nursing Skills Laboratory. Data collection tools will be administered three times: pre-test, post-test, and retention test. Only the "CORE Satisfaction Form" will be administered to students in the intervention group to assess their satisfaction after the CORE application. Descriptive statistics and the Student's t-test, Mann-Whitney U-test, t-test and Wilcoxon signed-rank test for dependent groups will be used in the analysis of the data.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
88

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 17, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

December 5, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

February 16, 2026

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 18, 2026

Completed
20 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 10, 2026

Completed
Last Updated

March 18, 2026

Status Verified

December 1, 2025

Enrollment Period

2 days

First QC Date

November 17, 2025

Last Update Submit

March 16, 2026

Conditions

Keywords

COREPain assessmentNursing educationAttitudeKnowledge

Outcome Measures

Primary Outcomes (1)

  • 1. Differences of knowledge scores between groups

    Pre-test, post-test and retention tests were applied to measure the level of knowledge. The 'Pain Knowledge Test', which was prepared by the researchers, will be used to assess knowledge levels. The test consists of ten questions. It will be marked out of 100. Test scores obtained at three different times will be compared. Higher post-test and retention test scores than pre-test scores suggest an increase in knowledge.

    To assess their knowledge levels, the pretest was administered in the first week, the posttest in the second week (1 day after the CORE application), and the retention test in the fourth week. Total duration: 4 weeks.

Secondary Outcomes (1)

  • Differences in Attitude Scores Towards Pain Assessment Between Groups

    To assess attitudes, a pre-test was administered in the first week, a post-test in the second week (1 day after the CORE application), and a retention test in the fourth week. Total duration: 4 weeks.

Study Arms (2)

CORE application

EXPERIMENTAL

During the study implementation process, a knowledge test and attitude scale will be administered as a pretest, posttest, and retention test. Case scenarios prepared for pain assessment will be applied to the intervention group students as CORE application.

Behavioral: CORE application

Control

NO INTERVENTION

During the study implementation process, a knowledge test and attitude scale will be administered as a pretest, posttest, and retention test.

Interventions

Case scenarios prepared for pain assessment will be applied to the intervention group students as CORE application.

CORE application

Eligibility Criteria

Sexall(Gender-based eligibility)
Gender Eligibility DetailsAll
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Volunteering to participate in research
  • Taking the Nursing Professional Courses Practicum II course
  • Participating in pain education
  • Participating in CORE training

You may not qualify if:

  • Not attending training
  • Not completing data collection tools

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Çankırı Karatekin University

Çankırı, 18200, Turkey (Türkiye)

Location

Related Publications (3)

  • Madenoğlu Kıvanç, M., Türen, S., Gül, A., Turan Miral, M., Atakoğlu Yılmaz, R., & Kara Özçalık, C. (2023). Hemşirelik eğitiminde öğrenci değerlendirme stratejisi: Objektif yapılandırılmış klinik sınavı. Sağlık ve Yaşam Bilimleri Dergisi, 5(2), 80-86. DOI: 10.33308/2687248X.202352301.

    BACKGROUND
  • Hakbilen HG, Ince S. Effect of Kegel Exercise-Focused Intervention on Urinary Incontinence in Elderly Women. J Wound Ostomy Continence Nurs. 2025 Mar-Apr 01;52(2):137-146. doi: 10.1097/WON.0000000000001162. Epub 2025 Mar 20.

    PMID: 40136104BACKGROUND
  • Turhan, K., Unsal, S., Kalaycı, N., Kayıkçı, V., & Uzun, E. (2006). Computer supported clinically oriented reasoning exam management system with client/server architecture: CORE-Builder. Current Developments in Technology-Assisted Education, 1203-1207.

    BACKGROUND

MeSH Terms

Conditions

Behavior

Study Officials

  • MÜJGAN ONARICI, PhD

    Çankırı Karatekin University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: The study will be conducted using a randomised controlled experimental design.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asst. Prof.

Study Record Dates

First Submitted

November 17, 2025

First Posted

December 5, 2025

Study Start

February 16, 2026

Primary Completion

February 18, 2026

Study Completion

March 10, 2026

Last Updated

March 18, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

in progress

Locations