Diagnosis of Delirium and Assessment of Sleep Quality in Patients in the Anesthesia and Intensive Care Unit
NCT ID: NCT06699004
Last Updated: 2024-11-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
107 participants
OBSERVATIONAL
2022-10-21
2023-01-21
Brief Summary
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Detailed Description
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Previous studies have indicated that medications used to control delirium can negatively affect sleep quality, while worsening sleep quality can exacerbate delirium. The main goal in preventing delirium is to ensure a regular sleep-wake cycle, support adequate fluid and nutrient intake, and provide both preventive and therapeutic treatments through a systematic, multidisciplinary team-based approach to reduce the frequency and duration of delirium. Artificial intelligence and machine learning approaches enable machines to simulate complex processes such as thinking and consciousness, thereby allowing computers to learn the relationships between inputs and outputs from large datasets, which helps them to make optimal decisions, analyses, and predictions. In the healthcare field, such technology is used in many areas, including the early detection and prediction of disease, disease classification, treatment, prevention of adverse outcomes, rapid analysis of clinical data, cost-saving initiatives, provision of effective and quality care, minimization of human errors, and clinical decision-making .
In the present study, the relationship between delirium and sleep quality in patients in the anesthesia and ICU was examined and a predictive analysis using a machine learning approach was performed.
The data required for this study were collected using the Patient Information Form, Nursing Delirium Screening Scale (Nu-DESC), Richards-Campbell Sleep Scale (RCSS), Richmond Agitation-Sedation Scale (RASS), and GCS. The collected data were analyzed using the SPSS statistical program (SPSS-26), and the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines were followed when reporting the results. The sample size was determined using the known population sample calculation method. Both frequency and percentage analyses were used to describe the distribution of the participants' demographic characteristics, while the mean and standard deviation were used to determine the participants' levels on the utilized scales. Cronbach's alpha reliability analysis was conducted to assess the scale reliability, and the post hoc power analysis showed that the study had medium power at a 95% confidence level with 99% significance . The skewness-kurtosis values were checked to assess the normality of the distribution. An independent samples t-test was used to assess the differences between groups. For comparisons among more than two groups, a one-way analysis of variance (ANOVA) was applied, while the prediction and receiver operating characteristic (ROC) curve analyses were conducted using R version 4.1.3.
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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İn our study there is only one group, and no intervention was made.
İn our study there is only one group, and no intervention was made.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients who have been hospitalized in the intensive care unit for at least 24 hours
* Patients not in a coma (RASS: between -3 and +4, GCS: 10 or above)
* Patients without a diagnosed dementia
* Patients without mental status disorders or psychological illnesses
* Patients who are willing to participate in the study
19 Years
ALL
Yes
Sponsors
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Sakarya University
OTHER
Responsible Party
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DİLEK KAYA
Principal Investigator
Principal Investigators
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dilek kaya, Msc. student
Role: PRINCIPAL_INVESTIGATOR
sakarya university health sciences institute
Locations
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Department of Internal Medicine Nursing, Faculty of Health Sciences, Sakarya University, 54050, Serdivan / SAKARYA.
Serdivan, Sakarya, Turkey (Türkiye)
Countries
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Other Identifiers
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E71522473050
Identifier Type: -
Identifier Source: org_study_id
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