Eyecontrol coMmunication Platform for dEliRium manaGemEnt in Intensive Care Units (EMERGE)
Completed · Not applicable · Has a placebo group
Conditions studied: Delirium, Delirium in Old Age, Critical Illness, Intensive Care Unit Delirium
In brief
The purpose of this research is to investigate whether addition of the EyeControl-Pro platform as an adjunct to standard guideline-based intensive care unit management of critically ill patients is effective in reducing delirium incidence and severity.
Key facts
- Study ID
- NCT06029244
- Run by
- Beth Israel Deaconess Medical Center
- People needed
- 160
- Starts
- 2024-02-25
- Expected to finish
- 2025-11-18
- Last updated by the study team
- 2025-12-03
Who can join
Age: 50 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Mechanically ventilated patients aged >=50 years
- RASS score of -3 to +1 and
- Anticipated to require >=24 hours of mechanical ventilation
You may not qualify if…
- Not expected to survive >=24 hours
- Have limitations in care (Do Not Resuscitate, or comfort-focused care orders)
- Receiving paralytic neuromuscular blocking agent (NMBA) infusion or anticipated need for NMBA use
- Have advanced dementia or cognitive impairment including post-concussive syndrome.
- Have severe uncorrected psychiatric disorders.
- Have uncorrected hearing or visual impairment.
- Acute or subacute neurological disorder hindering communication or ability to participate in CAM ICU assessments
- Enrolled in a clinical trial which prohibits co-enrollment.
- Incarcerated
- Have no identified legally appointed representative (LAR)
- Are unable to communicate in the predominant local language (English at US site and English/Hebrew/Arabic/Russian in Israel)
- Refusal of treating clinical team.
Where it is running
- Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
- Assuta Ashdod Medical Center — Ashdod, Israel
- Rabin Medical Center — Petah Tikva, Israel
Full record on ClinicalTrials.gov
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