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ED-TREAT (Early Detection and Treatment to Reduce Events With Agitation Tool) Compared to Usual Care

NCT04959279 · Status: SUSPENDED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2026-03-12

No results posted yet for this study

Summary

The purpose of this study is to conduct a a pilot trial that tests the acceptability, fidelity, and feasibility of ED-TREAT.

Conditions

  • Psychomotor Agitation
  • Behavioral Disorder

Interventions

OTHER

ED-TREAT

Patients will be assessed and treated based on a clinical decision support system.

Sponsors & Collaborators

  • National Institute of Mental Health (NIMH)

    collaborator NIH

  • Yale University

    lead OTHER

Principal Investigators

  • Ambrose H. Wong, (203) 737-2489 · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-01
Primary Completion
2026-08-01
Completion
2026-08-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04959279 on ClinicalTrials.gov