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Asthma Navigator Intervention to Improve Health Equity in Children

Emory University logo

Emory University

Status

Enrolling

Conditions

Asthma in Children

Treatments

Behavioral: The asthma navigator

Study type

Interventional

Funder types

Other

Identifiers

NCT06513832
STUDY00007482

Details and patient eligibility

About

The goal of this study is to improve health equity in children aged 5-16.9 years admitted to the PICU for asthma. The objectives are:

  • To identify the factors related to differential experiences of asthma self-management
  • To pilot the effectiveness of an individualized asthma navigator intervention at PICU discharge.

Full description

Despite available asthma treatments, nearly 50% of children with asthma experience exacerbations annually, with disadvantaged children, particularly Black and Hispanic, being the most affected. These disparities are largely due to social determinants of health (SDOH), including socioeconomics and family hardship, which explain over 80% of the racial disparities in asthma outcomes. Children in lower opportunity neighborhoods face additional challenges like poor housing and limited green spaces, increasing exposure to pollutants and allergens.

At Children's Healthcare of Atlanta's Pediatric ICU (PICU), 85% of asthma admissions come from low-opportunity areas, with 36.7% having another exacerbation within a year. Significant barriers to better outcomes include limited provider understanding of SDOH and challenges in asthma self-management. Effective asthma self-management, supported by medical providers, is crucial for improving health outcomes in these disadvantaged children.

Enrollment

75 estimated patients

Sex

All

Ages

5 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Admitted to the PICU for asthma

Exclusion criteria

  • Cystic fibrosis
  • Immune deficiency
  • Prematurity <35 weeks
  • Gestation and congenital airway deformities
  • Non-English speaker

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

75 participants in 2 patient groups

The Asthma Navigator
Experimental group
Description:
The Children's electronic medical record (EMR) of each child will be screened weekly for up to 52 weeks. When an asthma exacerbation prompting unscheduled healthcare utilization is noted (primary outcome), or at the end of 52 weeks, participant involvement in the study will end.
Treatment:
Behavioral: The asthma navigator
Standard of Care
No Intervention group
Description:
This arm will not have access to the Asthma Navigator. The Children's EMR of each child will be screened weekly for up to 52 weeks. When an asthma exacerbation prompting unscheduled healthcare utilization is noted (primary outcome), or at the end of 52 weeks, participant involvement in the study will end.

Trial contacts and locations

1

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Central trial contact

Anne Fitzpatrick, PhD, APRN

Data sourced from clinicaltrials.gov

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