RECRUITING

Critical Health Assessment and Outcomes Score/Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Critical Health Assessment and Outcomes Score/Study

Quick Facts

Study Start:2019-09-01
Study Completion:2027-09-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT02766166

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * All patients age 18-100 years admitted to a bed or OR with telemetry monitoring capability will be included.
  1. * Children (individuals \<18 years of age).

Contacts and Locations

Study Contact

Deeptankar DeMazumder, MD, PhD
CONTACT
513-558-1035
DDeMazu@iu.edu
Deeptankar DeMazumder, MD, PhD
CONTACT
513-558-1035
Deeptankar@gmail.com

Study Locations (Sites)

Indiana University
Indianapolis, Indiana, 46202
United States
Johns Hopkins University
Baltimore, Maryland, 21205
United States
University of Cincinnati
Cincinnati, Ohio, 45267-0542
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-09-01
Study Completion Date2027-09-01

Study Record Updates

Study Start Date2019-09-01
Study Completion Date2027-09-01

Terms related to this study

Additional Relevant MeSH Terms

  • Critical Illness
  • Death, Sudden