The Puerto Rico Asthma Integrated Response Program (PR-AIR)

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 12
Healthy Volunteers: f
View:

• 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

Locations
United States
Rhode Island
Rhode Island Hospital
ACTIVE_NOT_RECRUITING
Providence
Other Locations
Puerto Rico
Medial Sciences Campus, University of Puerto Rico
RECRUITING
San Juan
Contact Information
Primary
Daphne Koinis Mitchell, PhD
dkoinismitchell@lifespan.org
401-793-8632
Backup
Elizabeth McQuaid, PhD, ABPP
elizabeth_mcquaid@brown.edu
401-444-7573
Time Frame
Start Date: 2024-12-16
Estimated Completion Date: 2027-07-31
Participants
Target number of participants: 480
Treatments
Active_comparator: Low-Intensity (Virtual) Intervention Implementation
During low intensity implementation, families of children with poorly controlled asthma will be referred to the remote version of HARP (HARP-V) and will receive CASE remotely (CASE-V). Children with not well controlled asthma will receive only CASE-V remotely.
Active_comparator: High Intensity (in-Person) Intervention Implementation
During high intensity implementation, all interventions are administered in person.~Specifically, families of children with poorly controlled asthma will receive in-person versions of HARP and CASE. Children with not well controlled asthma will receive an in-person version of CASE only.
Related Therapeutic Areas
Sponsors
Collaborators: University of Puerto Rico
Leads: Rhode Island Hospital

This content was sourced from clinicaltrials.gov