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NCT06216483 · ClinicalTrials.gov registry record · NA
Using EMR Data and AI to Develop a Passive Digital Marker to Predict Postoperative Delirium
A NA study of Delirium in Old Age, sponsored by Indiana University.
- Active
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT06216483: Active NA study of Delirium in Old Age, sponsored by Indiana University.
NCT06216483 is a NA study of Delirium in Old Age that is active but no longer recruiting, run by Indiana University. The registered enrollment target is 60 participants, below the 523-participant average among 4 other Delirium in Old Age trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06216483, a NA study of Delirium in Old Age, is active but no longer recruiting, sponsored by Indiana University.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
The number of subjects diagnosed with delirium via the 3D-CAM questionnaire will be measured. The 3D-CAM is a brief verbal assessment tool that can be used to test patients and study participants for delirium via the Confusion Assessment Method (CAM). The 3D-CAM assessment is scored as either delirium present or delirium not present. Participants will be evaluated daily during the acute post-operative phase of the study (Post-Operative Days 0-7).
Conditions Studied
Interventions
- OTHER PDM Alert
Study Locations (1)
Indiana
- Indiana University Health University Hospital - Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2024-07-23 |
| Est. Completion | 2026-06-30 |
| Phase | NA |
What the registry record for NCT06216483 still lists
NCT06216483 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 523-participant average among 4 other Delirium in Old Age trials with a reported enrollment target (89% lower).
The record links to 1 condition, with Delirium in Old Age appearing as the primary indexed condition, and to 1 intervention - of which PDM Alert is the first listed.
NCT06216483 reports a single indexed study location in Indiana.
Frequently Asked Questions
What is clinical trial NCT06216483 about?
NCT06216483 is a clinical study titled "Using EMR Data and AI to Develop a Passive Digital Marker to Predict Postoperative Delirium". 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 ...
What is the current status of trial NCT06216483?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-07-23. Estimated completion is 2026-06-30.
What conditions does trial NCT06216483 study?
This clinical trial studies the following conditions: Delirium in Old Age.
What interventions are being tested in trial NCT06216483?
The interventions under investigation include: PDM Alert (OTHER).
Who is sponsoring clinical trial NCT06216483?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06216483 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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