Ankara University Ibni Sina Research and Application Hospital
Ankara, Turkey (Türkiye)
Location status: Recruiting
Location contact
Gurbet Baduryeri, MSc
CONTACT
Gurbet Baduryeri, MSc
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07779395
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Ankara, Turkey (Türkiye)
Location status: Recruiting
Gurbet Baduryeri, MSc
CONTACT
Gurbet Baduryeri, MSc
PRINCIPAL_INVESTIGATOR
This interventional before-and-after study is conducted in the Anesthesiology and Reanimation Intensive Care Unit of Ankara University Ibni Sina Research and Application Hospital. Adult patients meeting the eligibility criteria are included during the pre-intervention and intervention periods.
The pre-intervention period is conducted from March 1, 2026, to May 31, 2026. During this period, pressure injury risk assessment, skin assessment, prevention, and nursing care are performed according to routine clinical practice. PRESS AI is not used during this period.
Following a training and implementation period in June 2026, PRESS AI is introduced into clinical practice. The intervention period is conducted from July 1, 2026, to September 30, 2026. PRESS AI incorporates Braden Scale risk assessment, skin and wound assessment, artificial intelligence-supported image analysis for pressure injury staging, and a pressure injury prevention and care algorithm to support nursing care planning.
The artificial intelligence-generated staging recommendation is used as clinical decision support and does not replace the nurse's clinical judgment. The final pressure injury stage is determined by the nurse. Patients are followed daily for the development of new pressure injuries during their intensive care stay. The incidence of hospital-acquired pressure injuries during the pre-intervention and intervention periods is compared to evaluate the effectiveness of the PRESS AI-supported approach.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 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.
Time frame: 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).
Newly developed hospital-acquired pressure injuries will be classified according to pressure injury stage. The number and proportion of pressure injuries in each stage will be determined and compared between the pre-intervention and PRESS AI intervention periods.
Time frame: 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 anatomical locations of newly developed hospital-acquired pressure injuries will be recorded. The number and proportion of pressure injuries according to anatomical location will be determined and compared between the pre-intervention and PRESS AI intervention periods.
Time frame: From intensive care unit admission until the first occurrence of a hospital-acquired pressure injury or intensive care unit discharge, whichever occurs first, during the 3-month pre-intervention and 3-month intervention periods.
The time from admission to the intensive care unit to the development of a new hospital-acquired pressure injury will be recorded in days for patients who develop a pressure injury. The time to pressure injury development will be evaluated and compared between the pre-intervention and PRESS AI intervention periods.
Contact information is provided by the study sponsor or research team.
Ankara Yildirim Beyazıt University
Other
Determination of Pressure Injury and İntegration Into Nursing Care Using Artificial İntelligence
Acronym: PRESS AI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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