ED-TREAT (Early Detection and Treatment to Reduce Events With Agitation Tool) Compared to Usual Care
Paused · Not applicable
Conditions studied: Psychomotor Agitation, Behavioral Disorder
In brief
The purpose of this study is to conduct a a pilot trial that tests the acceptability, fidelity, and feasibility of ED-TREAT.
Key facts
- Study ID
- NCT04959279
- Run by
- Yale University
- People needed
- 26
- Starts
- 2026-04-01
- Expected to finish
- 2026-08-01
- Last updated by the study team
- 2026-03-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- adult (age≥18) patients presenting to the YNHH ED during the pilot trial period
- deemed to have a mild-moderate or high risk of agitation as determined by ED-TREAT
- do not require physical restraint orders <30 minutes of arrival
- with a score of "4" (quiet and awake; normal level of activity) on the Behavioral Activity Rating Scale
- have comfort with conversational English
- able to provide verbal consent.
You may not qualify if…
- Presence of a restraint order <30 minutes of arrival and presence of a non-violent physical restraint order where indications are not due to agitation (e.g., for protecting intubation or life-preserving equipment)
Where it is running
- Yale New Haven Hospital — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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