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Community Health Equity Accelerator (CHEA) Pediatric Asthma Intervention

Yale University logo

Yale University

Status

Active, not recruiting

Conditions

Asthma in Children

Treatments

Behavioral: Promotora Home Visit

Study type

Interventional

Funder types

Other

Identifiers

NCT06507943
2000037314

Details and patient eligibility

About

The purpose of this pilot is to initiate an academic-community partnership and launch a multi-level intervention that includes an asthma exposure pathway (an online decision support and resource) and a health Promotora program that will provide culturally responsive asthma support alongside legal and medical services to improve access to asthma care and ultimately improve asthma-related outcomes in the New Haven region.

Full description

In this will be a prospective, non-randomized, observational, multi-level pilot intervention, general pediatricians and specialists in New Haven, Connecticut will utilize a newly developed clinical pathway that will be publicly available at the Yale Pediatrics Clinical Pathways website and accessible within the electronic health record (EHR) via integrated software to submit referrals for participants in a Promotora (Community Health Worker) asthma home-visiting intervention.

The Hispanic Federation Promotoras, who are partners in this study who have received Human Subjects research training, will enroll participants in the study. For each participating family, Promotora home visits will be scheduled 6-8 weeks apart, with in-person or virtual visits conducted per the family's preference. The Promotoras, who have received specialized asthma training, will address concerns raised by families, using the clinical pathway as a resource (the pathway will have resources for asthma-related concerns that are raised). A clinician from the study team will be on call at all times for the Promotoras in case urgent questions arise, and weekly case-conferences will be arranged to discuss any additional needs for support.

In this study, the primary outcomes will include measures of feasibility of both Promotora home visits and pathway utilization. The investigators will evaluate secondary outcomes using an interrupted time series analysis to evaluate asthma-related outcomes. In addition to survey data, asthma exacerbation metrics will be collected from the electronic health record.

Enrollment

50 estimated patients

Sex

All

Ages

4 to 11 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Children with a diagnosis of asthma with at least one of the following:

  • Oral steroid prescription in past 12m
  • ED visit for asthma in past 12m
  • Hospital admission for asthma in past 12m
  • Asthma control test (ACT) score at visit ≤19
  • Concern for asthmogenic exposure in the home (such as mold, pests, smoking, or pollution)
  • At least one missed follow-up appointment for asthma
  • At least one asthma exacerbation in the prior year
  • Interested in asthma education (such as education in how to prevent asthma or how to administer medications)
  • Concern for medication non-adherence

Exclusion criteria

  • Living outside of New Haven Zip Code

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Promotora
Experimental group
Description:
Two Hispanic Federation Promotoras (community health workers) will provide culturally competent, bilingual home visits for asthma-related education and evaluation and support for health-harming legal needs (e.g., mold, rodents), including an initial visit and a follow-up visit 6-8 weeks later.
Treatment:
Behavioral: Promotora Home Visit

Trial contacts and locations

1

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Central trial contact

Julie Flom, MD MPH; Julia Rosenberg, MD MHS

Data sourced from clinicaltrials.gov

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