International Multicenter Study One Day Prevalence Observational Study for Delirium on ICU
IMPROVE-ICU
1 other identifier
observational
1,002
1 country
1
Brief Summary
An anonymous international multicenter - clinical survey, one-day observational study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2011
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2011
CompletedFirst Submitted
Initial submission to the registry
January 18, 2011
CompletedFirst Posted
Study publicly available on registry
January 19, 2011
CompletedAugust 13, 2013
August 1, 2013
Same day
January 18, 2011
August 9, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Implementation rate of routine delirium assessment
24 hours
Secondary Outcomes (6)
Point prevalence of ICU delirium
24 hours
Methodology of delirium assessment (e.g. type of score, frequency of evaluation)
24 hours
Non-pharmacological treatment-/prevention strategies
24 hours
Drugs used for delirium treatment
24 hours
Sedation practices (e.g. scales, daily sedation goals, SBT - spontaneous breathing trials, SAT - spontaneous awakening trials)
24 hours
- +1 more secondary outcomes
Study Arms (1)
Critically ill patients
Patients staying in the ICU on the 25th of January
Eligibility Criteria
ICU patients
You may qualify if:
- Patients staying in the ICU on the 25th of January (one-day prevalence study)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Claudia Spieslead
- European Society of Intensive Care Medicinecollaborator
Study Sites (1)
Department of Anesthesiology and Intensive Care Medicine, Campus Virchow-Klinikum and Campus Charité Mitte, Charité - Universitaetsmedizin Berlin
Berlin, State of Berlin, 13353, Germany
Related Publications (1)
Luetz A, Balzer F, Radtke FM, Jones C, Citerio G, Walder B, Weiss B, Wernecke KD, Spies C. Delirium, sedation and analgesia in the intensive care unit: a multinational, two-part survey among intensivists. PLoS One. 2014 Nov 14;9(11):e110935. doi: 10.1371/journal.pone.0110935. eCollection 2014.
PMID: 25398099DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Claudia Spies, MD
Charité - Universitaetsmedizin Berlin
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Prof. Dr. C. Spies, MD, Department of Anesthesiology and Intensive Care Medicine, Campus Virchow Klinikum and Campus Charité Mitte, Charité - Universitaetsmedizin Berlin
Study Record Dates
First Submitted
January 18, 2011
First Posted
January 19, 2011
Study Start
January 1, 2011
Primary Completion
January 1, 2011
Study Completion
January 1, 2011
Last Updated
August 13, 2013
Record last verified: 2013-08