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NCT06216483
Using EMR Data and AI to Develop a Passive Digital Marker to Predict Postoperative Delirium
Conditions: Delirium in Old Age
Sex: All
Ages: 65 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 60
Sponsor: Indiana University
Location: Indiana University Health University Hospital Indianapolis Indiana
Summary
This study will be a pilot randomized controlled trial that will determine the effect of an indicator of delirium risk, which will be delivered either via a paper form or via the electronic medical record, on (1)postoperative delirium incidence; and (2)the development of long term cognitive decline and dementia.
Eligibility Criteria
Inclusion Criteria:
65 years old Planned inpatient major surgery requiring inpatient stay ≥ 1 day
Exclusion Criteria:
* Baseline cognitive impairment or a diagnosis of Alzheimer's Disease/Alzheimer's Disease and Related Dementias (AD/ADRD)
* Alcohol or drug withdrawal
* Prisoner status
* Unable to communicate with research staff due to sensory impairments
* Not fluent in English
* Currently has a personal safety attendant
Source: ClinicalTrials.gov (NCT06216483). StuddyBuddy aggregates publicly available trial information.