- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05384964
Nurses' Knowledge, Barriers and Practices in the Assessment of Delirium in the Intensive Care Unit
Delirium in intensive care patients is a complication associated with many adverse consequences. It negatively affects patient outcomes, is an independent predictor of mortality, prolongs intensive care unit (ICU) stay and causes cognitive impairment. It is estimated that delirium affects up to 80% of ICU patients. Unfortunately, delirium still remains undiagnosed in many cases. Due to the high prevalence of this complication in critically ill patients, it is important to implement an effective management protocol to prevent delirium.
Nurses' knowledge of delirium, learning about nursing practices and identifying barriers to delirium assessment, may be an important basis for early recognition and the creation of procedures for delirium prevention in the intensive care unit.
Study Overview
Status
Intervention / Treatment
Detailed Description
The survey questionnaire is aimed at nurses working in the intensive care unit.
First, respondents are asked to answer questions on socio-demographic data. Then, two questionnaires were used to conduct the study:
The Nurses' Knowledge of Delirium questionnaire.
The questionnaire consists of two parts:
- The first part deals with questions related to the definition of delirium and the tools used to detect specific conditions.
- In the second part, participants are asked to answer questions about delirium and its associated risk factors by ticking respectively "agree", "disagree" or "not sure" to a series of 28 statements.
Fourteen of these statements relate to delirium, its symptoms and management, and 14 relate to risk factors for delirium.
- Nursing Practices and Perceptions Towards Delirium in the Intensive Care Unit questionnaire.
The questionnaire consists of two parts:
- The first part consists of questions about sedation and delirium assessment.
- The second part deals with practices/opinions about delirium and its assessment, including identification of potential barriers to delirium assessment
Consents were obtained from the authors for the use of both research tools. Completion of the questionnaire is voluntary, anonymous and equivalent to giving informed consent to participate in the study.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Gdansk/Pomorskie, Poland
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Gdańsk, Gdansk/Pomorskie, Poland, Poland, 80-211
- Department of Internal and Pediatric Nursing/ Department of Anesthesiology Nursing & Intensive Care
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Nurses,
- ICU staff.
Exclusion Criteria:
- Other medical staff,
- children's ICU staff,
- nurses working in other departments.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Nurses
|
Questionnaire completed by ICU nurses
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge of delirium
Time Frame: 4 month
|
Assessment of nurses' knowledge of delirium in the intensive care unit using The Nurses' Knowledge of Delirium questionnaire.
|
4 month
|
|
Barriers to delirium assessment
Time Frame: 4 month
|
Identifying barriers to assessment and treatment of delirium in the intensive care unit using The Nursing Practices and Perceptions Towards Delirium in the Intensive Care Unit questionnaire.
|
4 month
|
|
Practices and perceptions of delirium
Time Frame: 4 month
|
Exploring nurses' practices and perceptions of delirium in the intensive care unit using The Nursing Practices and Perceptions Towards Delirium in the Intensive Care Unit questionnaire.
|
4 month
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NKBBN/267/2022
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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