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RecruitingNCT07779395PRESS AIUpdated Aug 21, 2026

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

An interventional study of PRESS AI-Supported Nursing Care in Pressure Injury, sponsored by Ankara Yildirim Beyazıt University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-21.

Sponsored by Ankara Yildirim Beyazıt University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Mar 2026, registered Aug 2026).
  • Started Mar 2026; still recruiting 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
174
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

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.

Read the detailed description

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.

02

Conditions studied

  • Pressure Injury

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Keywords

  • Pressure Injury
  • Artificial Intelligence
  • Nursing Care
  • Intensive Care
  • Clinical Decision Support
  • Mobile Application
  • Pressure Injury Prevention
03

In context

Pressure Ulcer

545 studies on the registry are indexed under Pressure Ulcer; 129 are open to participants now.

This study's planned enrollment of 174 is above the median of 70 across 405 interventional studies indexed under Pressure Ulcer.

Browse Pressure Ulcer studies →

Lead sponsor

Ankara Yildirim Beyazıt University is the lead sponsor of 241 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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 provided by the patient or, when the patient lacks decision-making capacity, by the patient's legally authorized representative.

Exclusion criteria

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.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

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05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
174 participants (estimated)

Study arms

  • No intervention
    Routine Nursing Care

    Participants in this arm receive routine pressure injury prevention and nursing care according to standard clinical practice. Pressure injury risk and skin assessments are performed using routine clinical procedures. The PRESS AI mobile application and its integrated pressure injury prevention and care algorithm are not used in this arm.

  • Experimental
    PRESS AI-Supported Nursing Care

    Participants in this arm receive pressure injury prevention and nursing care supported by the PRESS AI mobile application and its integrated pressure injury prevention and care algorithm. PRESS AI supports pressure injury risk assessment, skin and wound assessment, artificial intelligence-assisted pressure injury staging, and planning of prevention and care interventions. The final pressure injury staging decision is made by the nurse based on clinical assessment.

    Other: PRESS AI-Supported Nursing Care

Interventions

  • OtherPRESS 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.

06

What researchers measure

Primary outcomes

  1. Incidence of Hospital-Acquired Pressure Injuries

    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).

Secondary outcomes

  1. Distribution of Pressure Injury Stages

    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).

  2. Anatomical Distribution of Pressure Injuries

    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: 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).

  3. Time to Development of Pressure Injury

    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.

    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.

07

Study locations

1 of 1 sites recruiting
  • Ankara University Ibni Sina Research and Application Hospital
    Ankara, Ankara, Turkey (Türkiye)
    Recruiting
    • Gurbet Baduryeri, MSc · Contactgurbet.bdr@gmail.com · +90-555-631-59-34
    • Gurbet Baduryeri, MSc · Principal investigator
08

References and documents

Individual participant data

Plan to share: No — Individual participant data sharing is not planned as part of the current study protocol.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07779395
Responsible party
Gurbet Baduryeri (Principal Investigator, Ankara Yildirim Beyazıt University) — Principal investigator
First posted
Aug 21, 2026
Start date
Mar 1, 2026
Primary completion
Sep 30, 2026 (estimated)
Completion
Sep 30, 2026 (estimated)
Last update
Aug 21, 2026

Study contacts

Gurbet Baduryeri, MSc
Contact
gurbet.bdr@gmail.com
+90-555-631-59-34
Hilal Tüzer, PhD
principal investigator · Ankara Yildirim Beyazıt University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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