Prevention of Delirium in ICU Using Multimodal Interventions
ConditionIntensive Care Unit Delirium
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorSeoul National University Hospital
About this trial
This study was designed to evaluate the impact of non-pharmacological multimodal interventions including ongoing orientation, sensory correction, setting of familiar circumstance and promotion of sleep enviromnet for prevention of delirium in intensive care unit.
Eligibility criteria
Qualifiers
Adult patients over 50 years who are expected to spend more than 24 hours in the intensive care unit
Disqualifiers
Patients who developed delirium before entering the intensive care unit
Patients with cognitive impairment
Patients who have hearing or vision deficits, or have difficulty in communication
Patients who are expected to die within 24 hours or do not want life-sustaining treatment
Trial design
Treatments tested in this trial
- Multimodal therapy for prevention of delirium
Treatment groups
196 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov