Actively Recruiting
Delirium Identification in Older Patients With Alzheimer's and Other Related Dementias In the Emergency Department
Led by Ohio State University · Updated on 2025-04-03
60
Participants Needed
1
Research Sites
98 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Delirium is highly prevalent and very bad for patients with dementia. Delirium is a dangerous medical condition that occurs in 6-38% of older Emergency Department patients and 70% of ICU patients. A person who develops delirium in the ED or hospital has a 12 times higher odds of being newly diagnosed with dementia in the next year compared to a similar patient who does not become delirious. Delirium is especially dangerous for persons living with Alzheimer Disease and Related Dementias (AD/ADRD). Persons living with ADRD have an almost 50% chance of developing delirium in the hospital. Clinicians are bad at recognizing delirium. A recent systematic review led by the Geriatric Emergency Care Applied Research network (NIH funded) found that current delirium screening tools are at most 64% sensitive, meaning that physicians can identify some phenotypes of delirium well, but cannot easily rule out delirium in acutely ill older patients. The investigators propose integrating wrist biosensors into the emergency management of older adults with dementia. The investigators will monitor heart rate variability, movement, and electrodermal activity (electrical activity of at the level of the skin) to determine if an array of biosensors more sensitive to delirium than current verbal screening tools.
CONDITIONS
Official Title
Delirium Identification in Older Patients With Alzheimer's and Other Related Dementias In the Emergency Department
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients 65 years or older with a known diagnosis of dementia or a strong suspicion or confirmation of dementia during this visit
- Emergency Department visit or hospitalization expected to last more than 4 hours from enrollment
You will not qualify if you...
- Currently intubated or on mechanical ventilation
- Undergoing a procedure requiring sedation
- Unable to consent due to cognitive impairment without a legally authorized representative or caregiver present
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Ohio State University Wexner Medical Center
Columbus, Ohio, United States, 43210
Actively Recruiting
Research Team
L
Lauren Southerland, MD MPH
CONTACT
M
Michael Hill, RN
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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