Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT02766166

Critical Health Assessment and Outcomes Score/Study

Led by Johns Hopkins University · Updated on 2022-10-10

200000

Participants Needed

3

Research Sites

417 weeks

Total Duration

On this page

Sponsors

J

Johns Hopkins University

Lead Sponsor

U

University of Cincinnati

Collaborating Sponsor

AI-Summary

What this Trial Is About

CHAOS is based on the investigator's new and exciting results from pre-clinical and large longitudinal multi-center observational clinical studies of critically ill patients and asymptomatic community-based adults with little or no advanced disease. By integrating approaches from the physical, biological, computational, statistical and clinical sciences, this observational study will test the hypothesis that early diagnosis of subclinical signatures of critical illness encoded within physiological signals complements conventional clinical predictors by providing unique prognostic insight. The primary goal is to reduce mortality, morbidity and complications by early identification of individuals with brewing subclinical critical illness and adverse events before overt clinical presentation (e.g., cardiac arrest, arrhythmias, hemorrhage, respiratory failure, circulatory collapse). This will provide the necessary lead time for healthcare providers to deliver early, more effective and/or preventive therapies. Through innovative approaches, CHAOS also meets the challenge of medical errors to reduce missed diagnosis, misdiagnosis, preventable harm and variability in provider adherence to best practice guidelines. The goal is to validate predictive algorithms and identify subclinical signatures of illness, ranging from asymptomatic adults in the community to very sick patients in the hospital. The overall goal is to make healthcare more precise, effective, efficient, safe and timely while reducing costs, preventable harms and adverse events.

CONDITIONS

Official Title

Critical Health Assessment and Outcomes Score/Study

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 100 years
  • Admitted to a hospital bed or operating room with telemetry monitoring capability
Not Eligible

You will not qualify if you...

  • Children under 18 years of age

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 3 locations

1

Indiana University

Indianapolis, Indiana, United States, 46202

Not Yet Recruiting

2

Johns Hopkins University

Baltimore, Maryland, United States, 21205

Not Yet Recruiting

3

University of Cincinnati

Cincinnati, Ohio, United States, 45267-0542

Actively Recruiting

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Research Team

D

Deeptankar DeMazumder, MD, PhD

CONTACT

D

Deeptankar DeMazumder, MD, PhD

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

2

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