Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
The Puerto Rico Asthma Integrated Response Program ("PR-AIR")
NCT05999032 · View on ClinicalTrials.gov ↗
Study Summary
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 Studied
Interventions
- BEHAVIORAL CASE in person version (High Intensity Package)
- BEHAVIORAL CASE-V remote version (Low Intensity Package)
- BEHAVIORAL CASE and HARP in person (High Intensity package)
- BEHAVIORAL CASE-V and HARP-V remote version (Low Intensity package)
Study Locations (2)
Rhode Island
- Rhode Island Hospital — Providence
Puerto Rico
- Medial Sciences Campus, University of Puerto Rico — San Juan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 480 participants |
| Start Date | 2024-12-16 |
| Est. Completion | 2027-07-31 |
| Phase | NA |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05999032
The ClinicalTrials.gov registry entry for NCT05999032 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 480 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rhode Island Hospital, which has 110 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Pediatric Asthma appearing as the primary indexed condition, and to 4 interventions — of which CASE in person version (High Intensity Package) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05999032 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Rhode Island, Puerto Rico. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05999032 about?
NCT05999032 is a clinical study titled "The Puerto Rico Asthma Integrated Response Program ("PR-AIR")". 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 impl...
What is the current status of trial NCT05999032?
This trial is currently recruiting. It is a NA study. The enrollment target is 480 participants. The study started on 2024-12-16. Estimated completion is 2027-07-31.
What conditions does trial NCT05999032 study?
This clinical trial studies the following conditions: Pediatric Asthma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05999032?
The interventions under investigation include: CASE in person version (High Intensity Package) (BEHAVIORAL), CASE-V remote version (Low Intensity Package) (BEHAVIORAL), CASE and HARP in person (High Intensity package) (BEHAVIORAL), CASE-V and HARP-V remote version (Low Intensity package) (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05999032?
This trial is sponsored by Rhode Island Hospital, which has 110 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05999032 being conducted?
This trial has 2 study locations across Rhode Island, Puerto Rico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.