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Clinical Trials/NCT06507943
NCT06507943
Active, not recruiting
Not Applicable

Community Health Equity Accelerator (CHEA): Community-Academic Asthma Partnership, Pediatric Asthma Intervention

Yale University1 site in 1 country50 target enrollmentSeptember 16, 2024

Overview

Phase
Not Applicable
Intervention
Promotora Home Visit
Conditions
Asthma in Children
Sponsor
Yale University
Enrollment
50
Locations
1
Primary Endpoint
Percent of clinicians who use pathway, to assess feasibility of asthma pathway use
Status
Active, not recruiting
Last Updated
3 months ago

Overview

Brief Summary

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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
September 16, 2024
End Date
December 31, 2027
Last Updated
3 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Arms & Interventions

Promotora

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.

Intervention: Promotora Home Visit

Outcomes

Primary Outcomes

Percent of clinicians who use pathway, to assess feasibility of asthma pathway use

Time Frame: One Year

Percent of clinicians at participating practices who have accessed the asthma intervention pathway (using data from pathway utilization metrics)

Percent of patients for whom the pathway is used, to assess feasibility of asthma pathway use

Time Frame: One Year

Percent of patients for whom a clinician accessed the asthma pathway (using pathway utilization metrics) out of total potential children for whom it could be used (using deidentified electronic health (EHR) record data tool)

Count of use of individual asthma pathway component use

Time Frame: One Year

Count of use of individual asthma pathway components (using pathway utilization metrics)

Percentage of Referrals Resulting in Home Visit, to Assess Feasibility of Promotora Visits

Time Frame: One Year

Percent of referred participants (from all referrals placed) to the newly-established asthma home visiting Promotora Program that resulted in a home visit (in-person or virtual)

Secondary Outcomes

  • Mean number of hospital admissions for asthma(Two years (year before and year after intervention))
  • Mean number of urgent visits for asthma(Two years (year before and year after intervention))
  • Mean number of oral steroid prescriptions for asthma(Two years (year before and year after intervention))
  • Mean Pediatric Quality of Life (Peds-QL) scores(Baseline and 6-8 weeks later)
  • Mean number of emergency department (ED) visits for asthma(Two years (year before and year after intervention))
  • Mean Asthma Control Test (ACT) for 4-11 years scores(Baseline and 6-8 weeks later)

Study Sites (1)

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