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Prediction of Pressure Injury Risk in ICU Using Data Mining

Prediction of Pressure Injury Risk in the Intensive Care Unit: A Comparative Analysis of Data Mining Algorithms in a Single-Center Retrospective Cohort

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07306143
Acronym
ICU
Enrollment
500
Registered
2025-12-29
Start date
2026-01-16
Completion date
2026-04-29
Last updated
2026-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pressure Injury

Keywords

Pressure injury risk, Data mining, Machine learning, Retrospective study, Risk prediction

Brief summary

This study is a retrospective record review conducted among adult patients hospitalized in the intensive care unit of a tertiary hospital between October 10, 2020, and October 10, 2025. The aim of the study is to predict the risk of pressure injury development using demographic, clinical, laboratory, and nursing care-related variables by applying multiple data mining algorithms. No intervention, treatment, or patient contact will occur. All data will be extracted from existing electronic and paper-based medical records and will be fully anonymized prior to analysis. The study poses no risk to participants and will be conducted with approval from the institutional review board or ethics committee.

Detailed description

This observational study uses a retrospective cohort design to analyze the clinical, demographic, laboratory, and nursing documentation records of adult intensive care unit (ICU) patients hospitalized between October 10, 2020, and October 10, 2025. The purpose of the study is to identify factors associated with the development of pressure injury and to compare the predictive performance of multiple data mining and machine learning algorithms, including logistic regression, decision trees, random forest, support vector machines, and gradient boosting models. Data collection will involve reviewing archived ICU records, patient files, and nursing observation forms. No new data will be collected directly from patients, and no medical interventions or prospective follow-up will be performed. All extracted data will be fully anonymized prior to analysis. The study will be conducted in accordance with ethical principles and has been approved by the Bolu Abant Izzet Baysal University Non-Interventional Clinical Research Ethics Committee. The expected outcome of this study is to identify the most accurate predictive model for pressure injury risk and to support clinical decision-making processes by contributing to early prevention strategies in the ICU.

Interventions

OTHERNo intervention

This is a retrospective observational study. No interventions will be applied. All data will be obtained from existing medical records.

Sponsors

Abant Izzet Baysal University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients hospitalized in the intensive care unit between October 10, 2020, and \* October 10, 2025 * Adult patients aged 18 years and older * Length of intensive care unit stay of at least 24 hours * Availability of complete and accessible electronic or paper-based medical records

Exclusion criteria

* Patients younger than 18 years * Intensive care unit stay shorter than 24 hours Incomplete, missing, or inconsistent electronic or paper-based medical records * Presence of a pressure injury diagnosed before or at the time of intensive care unit admission * Inability to extract pressure injury-related data from medical records

Design outcomes

Primary

MeasureTime frameDescription
Prediction accuracy of pressure injury development10 October 2020 to 10 October 2025The primary outcome is the predictive accuracy of data mining algorithms in identifying the risk of developing pressure injury among patients hospitalized in the intensive care unit (ICU). Accuracy metrics such as the area under the receiver operating characteristic curve (AUC), sensitivity, specificity, precision, recall, and F1-score will be calculated using retrospective medical record data.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORSaadet Can Çiçek, Assoc. Prof., PhD

Abant Izzet Baysal University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026