Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 12:29 AM
Ignite Modification Date: 2025-12-25 @ 12:29 AM
NCT ID: NCT02319967
Eligibility Criteria: Inclusion criteria (all of the following): 1. Child is 5-11 years of age (a population in whom a diagnosis of asthma is generally reliable, and in whom exacerbations are common); 2. Child is presenting to the ED, urgent care center, or observation unit at a participating clinical center (Anne and Robert H. Lurie Children's Hospital of Chicago, Sinai Health System's Mount Sinai Hospital, John H. Stroger Jr. Hospital of Cook County Health \& Hospitals System, Rush University Medical Center, University of Chicago Medicine Comer Children's Hospital, and the University of Illinois Hospital \& Health Sciences System); 3. Child is treated with at least 1 dose of an inhaled or nebulized short-acting bronchodilator (quick-relief medication); 4. Child received systemic corticosteroids in the ED OR the caregiver reported at least 1 additional acute care visit for asthma in the previous 6 months (defined as an asthma-related ED visit or urgent care visit, or course of systemic corticosteroids); 5. Child and caregiver approached at least 1 hour after receipt of the first dose of quick-relief medication or systemic corticosteroids, whichever occurred first; 6. Diagnosis of asthma exacerbation by treating clinician; 7. Treating ED clinician indicates the child is likely to be discharged to home; and 8. Caregiver reports that English or Spanish is the preferred language at home. Exclusion criteria (none of the following): 1. Caregiver declines to provide informed consent, or the child declines to provide assent; 2. Child is admitted to an intensive care unit or transferred to another healthcare facility; 3. Child or another member of the child's primary household is a current or previous participant in the CHICAGO Plan; 4. Child is enrolled in another study involving a health-related intervention; 5. A CHW is already visiting the home as part of another program; 6. Child does not reside in Chicago.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 5 Years
Maximum Age: 11 Years
Study: NCT02319967
Study Brief:
Protocol Section: NCT02319967