Artificial Intelligence-Supported Pressure Injury Prevention and Care in Intensive Care Patients

NCT07779395 · tracked via the Priya Life Science Turkey tracker

Sponsor

Ankara Yildirim Beyazıt University

Phase

Not applicable

Started

2026-03-01

Last updated

2026-08-21

Condition(s) studied

Pressure Injury

Investigational drug(s) / intervention(s)

PRESS AI-Supported Nursing Care

PRESS AI-Supported Nursing Care: PRESS AI is an artificial intelligence-supported mobile clinical decision support application integrated with a pressure injury prevention and care algorithm. It supports nurses in Braden Scale risk assessment, skin and wound assessment, artificial intelligence-assisted pressure injury staging, and the planning and documentation of individualized pressure injury prevention and care interventions. Artificial intelligence-generated staging recommendations are used to support clinical decision-making and do not replace nurses' clinical judgment. The final pressure injury stage is determined by the nurse based on clinical assessment.

Study summary

This study evaluates the effect of an artificial intelligence-supported mobile application, PRESS AI, on pressure injury prevention and nursing care in adult intensive care patients. The application supports nurses in pressure injury risk assessment, wound assessment and staging, and selection of appropriate prevention and care interventions. The study compares the incidence of hospital-acquired pressure injuries before and after the implementation of PRESS AI. During the pre-intervention period, patients receive routine pressure injury prevention and nursing care. During the intervention period, nurses use PRESS AI together with an integrated pressure injury prevention and care algorithm to support clinical assessment and care planning.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Aged 18 years or older. * Hospitalized in the Anesthesiology and Reanimation Intensive Care Unit of Ankara University Ibni Sina Research and Application Hospital during the pre-intervention or intervention period. * Written informed consent provided by the patient or, when the patient lacks decision-making capacity, by the patient's legally authorized representative. Exclusion Criteria: * Refusal to participate by the patient or legally authorized representative, or withdrawal of previously provided consent. * Missing essential follow-up data required to assess the development of pressure injuries.

Primary outcome measure(s)

Incidence of Hospital-Acquired Pressure Injuries — Daily during each participant's intensive care unit stay; assessed over the 3-month pre-intervention period (March 1-May 31, 2026) and the 3-month intervention period (July 1-September 30, 2026).
The incidence of hospital-acquired pressure injuries will be determined based on newly developed pressure injuries during the intensive care unit stay. Patients will be assessed daily for pressure injury development, including the date of occurrence, anatomical location, and stage. The incidence during the pre-intervention period will be compared with the incidence during the PRESS AI intervention period.

Trial sites (1)

Facility	City	Region	Status
Ankara University Ibni Sina Research and Application Hospital	Ankara	Ankara	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07779395 on ClinicalTrials.gov ↗ ← All trials in Turkey