Actively Recruiting
The Puerto Rico Asthma Integrated Response Program ("PR-AIR")
Led by Rhode Island Hospital · Updated on 2025-08-20
480
Participants Needed
2
Research Sites
136 weeks
Total Duration
On this page
Sponsors
R
Rhode Island Hospital
Lead Sponsor
U
University of Puerto Rico
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to adapt and deliver an evidence-based multi-level intervention to reduce asthma disparities, and that promote and improve population health in the high-burden communities of San Juan, Puerto Rico. The Puerto Rico-Asthma Integrated Response Program (PR-AIR) will be implemented and evaluated to address pediatric asthma disparities in San Juan, PR, an area of high asthma burden. This study unfolds in two phases: In Phase 1, the researchers will collaborate with community stakeholders to identify needs, barriers and facilitators of PR-AIR implementation. Phase 2 consists of an evaluation of low-intensity (virtual) and high-intensity (in-person) methods of PR-AIR implementation outcomes using the RE-AIM (Reach, Effectiveness, Adoption, Implementation, and Maintenance) framework and a mixed methods approach.
CONDITIONS
Official Title
The Puerto Rico Asthma Integrated Response Program ("PR-AIR")
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children between the ages of 2 and 12 years old
- Children must reside in one of the identified catchment areas
- Children must meet the screening criteria as having not well controlled or poorly controlled asthma
You will not qualify if you...
- Children with complex medical conditions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Rhode Island Hospital
Providence, Rhode Island, United States, 02903
Active, Not Recruiting
2
Medial Sciences Campus, University of Puerto Rico
San Juan, Puerto Rico, Puerto Rico, 00937
Actively Recruiting
Research Team
D
Daphne Koinis Mitchell, PhD
CONTACT
E
Elizabeth McQuaid, PhD, ABPP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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