NCT07105696

Brief Summary

Health diagnosis is an essential part of the professional nursing role and the holistic nursing approach. The goal of the health diagnosis process is to establish a baseline database for the care plan, encompassing the patient's health status, risk factors related to their current health status, and health education needs. This process involves obtaining the patient's health history, conducting a physical examination, collecting other relevant data from the patient's health records, and recording the data identified. Collecting and analyzing information about the patient's health status begins with diagnosis. Diagnosis is the comprehensive and systematic process of collecting data to obtain information about the patient's current and past health status and to identify coping strategies used in cases of health deviations. Diagnosis enables the creation of a comprehensive database of the patient's health status. Therefore, one of the most important stages of the diagnostic process is the physical examination. The purpose of the physical examination is to collect detailed, objective data regarding the patient's physiological state. Physical examination is the ability to interpret what is seen, heard, and felt regarding the patient's condition. Inspection, palpation, auscultation, and percussion methods allow for the validation of data obtained through the nursing history and the acquisition of new data. Appropriate, accurate, and timely health diagnosis is the cornerstone of maintaining patient safety. Furthermore, because health diagnosis and physical examination require a comprehensive assessment of all body systems, they also facilitate improved communication and collaboration among nurses, patients, and other healthcare team members. Therefore, health diagnosis is an important component of nursing education. Health diagnosis is a clinical problem. Decision-making is one of the most important skills required to solve a clinical problem. In nursing education, curricula need to be developed to develop clinical thinking and problem-solving skills in students. There is often no single right or wrong in the relationship between the patient and the nurse. In such cases, the Clinically Oriented Reasoning Exam (CORE) is used to teach cause-effect relationships. CORE develops reasoning skills in decision-making. The classic CORE application is conducted in a laboratory setting. Each table in the laboratory is considered a station, and for each station, a clinical case is prepared in a format the student can understand. Information about the case is recorded on the front and back of the cards. The student is asked to answer, and depending on the correct step level, the student is given a negative or positive score. When the student turns the card over, they receive feedback on the question. The first student and the observer go to the first station, where the student reads the case and turns over as many cards as they want. Each card turned over is recorded. When a station is completed, the cards are rearranged to their original positions, and the student and observer move on to the next station. Another student returns with their observer to the previous station. Completion of all stations signifies completion of the exam. Conducting the traditional CORE is time-consuming and difficult. To eliminate the disadvantages of CORE and make the exam more effective, a web-based application method will be used. This will facilitate the assessment phase. The research was planned as a randomized controlled experimental study. The research question for this study was to determine the effectiveness of the digital CORE application on health diagnostic skills. Additionally, the relationships between the digital CORE application and demographic variables will be examined. The findings will be discussed with the contribution of literature, and recommendations for further research will be presented. The findings will provide insights into the variables associated with the digital CORE application, skill effectiveness, and achievement.

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 Nov 2024

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

November 20, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 15, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

July 13, 2025

Completed
24 days until next milestone

First Posted

Study publicly available on registry

August 6, 2025

Completed
Last Updated

August 6, 2025

Status Verified

July 1, 2025

Enrollment Period

2 months

First QC Date

July 13, 2025

Last Update Submit

July 29, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Clinical reasoning performance measured by the web-based Clinical Oriented Reasoning Exam (CORE) \[Score range: 0-100; higher scores indicate better performance]

    The CORE is a standardized web-based test that evaluates students' clinical reasoning skills through case-based scenarios. It is administered at the conclusion of the four-week educational program, and results will be aggregated and reported as mean ± standard deviation (SD).

    Week 4 (immediately after completion of the four-week module covering gastrointestinal, respiratory, cardiovascular, and musculoskeletal system assessments)

Secondary Outcomes (1)

  • Knowledge retention measured by the follow-up recall quiz \[Score range: 0-100; higher scores indicate better retention]

    Week 6 (two weeks after completion of the web-based Clinical Oriented Reasoning Exam \[CORE])

Study Arms (2)

Web-Based CORE

EXPERIMENTAL

The intervention planned for the study is a web-based digital CORE method. Students in the intervention group taking the Health Diagnosis course will be administered a web-based digital CORE to assess the cardiovascular, respiratory, musculoskeletal, and gastrointestinal systems.

Other: Web-Based CORE

Control Group

NO INTERVENTION

Control group students will be asked the same multiple-choice questions in a digital environment, assessing the cardiovascular, respiratory, musculoskeletal, and gastrointestinal systems.

Interventions

The intervention planned for the study is a web-based digital CORE method. Students in the intervention group taking the Health Diagnosis course will be administered a web-based digital CORE to assess the cardiovascular, respiratory, musculoskeletal, and gastrointestinal systems. Students in the experimental group will be administered the web-based digital CORE exam. Students in the control group will be asked the same multiple-choice questions in a digital environment. Two weeks later, students in the experimental and control groups will be administered another exam. Differences in achievement scores between the two groups will be evaluated.

Web-Based CORE

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • first-time enrollment in a health diagnosis course
  • volunteering to participate in the study

You may not qualify if:

  • not attending class and being absent
  • not wanting to participate in research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Suleyman Demirel University

Isparta, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
In the randomization process, those who meet the criteria for inclusion in the sample and accept to participate in the study do not know that they will be included in the intervention group or the control group, so it will be single-blind.
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor Research Assistant

Study Record Dates

First Submitted

July 13, 2025

First Posted

August 6, 2025

Study Start

November 20, 2024

Primary Completion

January 15, 2025

Study Completion

February 15, 2025

Last Updated

August 6, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations