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Clinical Trials in Turkey / NCT07171944
Starting soon Not applicable

Effects of Artificial Intelligence Nurse Orientation Program on Psychological Outcomes and Length of Hospital Stay in Intensive Care Unit

NCT07171944 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-11-01
Last updated
2025-09-15

Condition(s) studied

DeliriumAnxiety and DepressionIntensive Care Units (ICUs)Artificial Intelligence (AI)NurseCritical CareOrientation

Investigational drug(s) / intervention(s)

Structured orientation programHuman Nurse

Structured orientation program: Artificial intelligence technology will be incorporated into the orientation training program developed for patients in the intensive care unit who are assigned to the intervention group. The program will be administered twice daily over a three-day period. In this group, delirium-free days will be tracked, changes in anxiety and depression levels will be evaluated, and the length of intensive care unit stay among patients who remain free of delirium through this intervention will be examined.

Human Nurse: Researchers will administer a structured orientation training program lasting approximately 10 minutes face-to-face to participants in the control group. This training program will be administered twice daily for 3 days. Following the training program, delirium-free days, anxiety and depression scores, and length of stay in the intensive care unit will be evaluated.

Study summary

Artificial intelligence (AI), now an integral part of healthcare services and presents numerous opportunities. Customized treatment plans, clinical decision support systems, predictive analysis for disease prevention, patient engagement and education, quality improvement, and error reduction are some of these opportunities. In the context of delirium prevention, risk assessment, and treatment planning, the AI-supported system AI-AntiDelirium is designed to standardize the approach to delirium management in alignment with the PADIS guidelines. A randomized controlled trial evaluating the effectiveness of this system found that the workload of nurses decreased, facilitated early diagnosis and prevention of delirium, and recommended evidence-based and individualized delirium interventions. A systematic review concluded that AI applications did not significantly impact the length of hospital stay and emphasized the need for further research. Also, AI platforms contributed to positive results in reducing anxiety and depression in patients. Furthermore, systematic reviews have demonstrated that AI-based chatbots are effective in alleviating symptoms of depression and anxiety. However, the literature includes a limited number of patient education programs specifically designed to prevent or manage delirium through AI-based approaches. Notably, there is a lack of studies comparing the effectiveness of AI-supported educational interventions with those delivered directly by nurses.

The goal of this clinical trial is to develop a structured AINurse and Human Nurse orientation training program for intensive care unit (ICU) patients and compare the effects of these training programs on ICU patients' delirium-free days, level of anxiety and depression, and length of stay in the ICU. Hypotheses of the study:

H1: Patients who receive the structured AINurse patient orientation training program will have longer delirium-free days than patients who receive Human Nurse orientation training.

H2: Patients who receive the structured AINurse patient orientation training program will have lower levels of anxiety and depression than patients who receive the Human Nurse orientation training.

H3: Patients who receive the structured AINurse patient orientation training program will have shorter lengths of stay in the intensive care unit than patients who receive the Human Nurse orientation training.

Researchers will compare the AINurse patient orientation training program and the orientation training program provided by human nurses in terms of patients' delirium-free days, level of anxiety and depression, and length of stay in the ICU.

* Those in the intervention group will receive the AINurse orientation training program twice daily for 3 days.
* Participants in the control group will receive face-to-face structured orientation training from researchers twice daily for 3 days.
* Delirium-free day assessment, anxiety and depression will be evaluated for patients in both groups over 3 days.
* The length of stay in the intensive care unit will be monitored for patients in both groups.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Intensive care unit confusion assessment scale (CAM-ICU scale) score of 0-2 * Age 18 years or older * Hospitalized in the intensive care unit for at least 24 hours * Glasgow coma scale score of 13-14-15 points * Richmond Agitation Sedation Scale (RASS) score between -1 and +1 * No hearing problems Exclusion Criteria: * Intensive care unit confusion assessment scale (CAM-ICU scale) score of 6-7 * Any psychiatric illness or impaired brain function * Defined hearing loss * Advanced dementia * Younger than 18 years of age * Richmond Agitation Sedation Scale (RASS) score outside the range of -1 to +1 * Who use sedative medication * History of surgery or disease around the ear

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Koç University Istanbul Turkey (Türkiye)

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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 NCT07171944 on ClinicalTrials.gov ↗ ← All trials in Turkey