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Completed Phase 4 Interventional Results available

Patient Empowered Strategy to Reduce Asthma Morbidity in Highly Impacted Populations; PeRson EmPowered Asthma RElief

ClinicalTrials.gov ID: NCT02995733

Public ClinicalTrials.gov record NCT02995733. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 4:22 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Patient Empowered Strategy to Reduce Asthma Morbidity in Highly Impacted Populations

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Asthma imposes a significant burden in the US in terms of morbidity, costs to society, individual suffering, loss of productivity and mortality. African Americans (AA) and Hispanic/Latinos (H/L) bear a disproportionate share of that morbidity. Despite national guidelines for asthma treatment, the gap between these groups and whites has been stable or widening. The need for pragmatic research to address the continuing burden is widely recognized. Patients use asthma reliever inhalers to provide immediate relief of symptoms. Controller inhalers (inhaled corticosteroids (ICS)) are intended to be used regularly to prevent symptoms and attacks. Guidelines suggest that they be used daily, on a fixed basis, in all but the mildest asthma. However, adherence by patients and implementation of evidence-based guideline recommendations by clinicians has been poor. Gap analysis suggests that it is difficult to improve adherence to the current recommendations without complex and resource-intensive interventions. Studies have examined symptom-activated use of ICS triggered by use of a reliever medication. The Investigators call this approach PARTICS - Patient Activated Reliever-Triggered Inhaled CorticoSteroid. Explanatory, non-real world studies suggest that PARTICS can produce up to 50% reductions in asthma attacks compared with usual care, while reducing ICS use by half or more. These studies have been performed in pre-selected populations, which represent less than 5% of asthma patients. The previous studies have been done with repeated education and adherence checks in both the intervention and control arms. The investigators have consulted with AA and H/L patients, health care providers, leaders of professional societies, advocacy groups, health policy leaders, pharmacists, and pharmaceutical manufacturers. All groups have indicated that asthma decision making would be changed if we demonstrated that implementing PARTICS improves important asthma outcomes such as reducing exacerbations. The Investigators have designed a study with the stakeholders to determine whether PARTICS can improve outcomes that are important to patients when superimposed on a background provider-educated standard of care through the Asthma IQ system. The Investigators propose a study entitled PREPARE: Patient Empowered Strategy to Reduce Asthma Morbidity in Highly Impacted Populations. The Investigators aim to determine whether PARTICS can reduce asthma morbidity in AA and H/L.

Study identification

NCT ID
NCT02995733
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
1,220 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 27, 2017 (Actual)
Primary completion
Apr 30, 2021 (Actual)
Completion
Apr 30, 2021 (Actual)
Last update posted
Jan 19, 2023

2017 – 2021

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294 —
University of Southern California Los Angeles California 90033 —
Denver Health and Hospital Authority Denver Colorado 80209 —
Yale University New Haven Connecticut 06510 —
University of Florida Gainesville Florida 32610 —
University of Miami Miami Florida 33136 —
Grace Medical Home Orlando Florida 32827 —
University of Central Florida Orlando Florida 32827 —
University of South Florida Tampa Florida 33613 —
University of Illinois- Chicago Chicago Illinois 60607 —
Baystate Health Center Springfield Massachusetts 01199 —
Mt. Sinai New York New York 10029 —
Montefiore The Bronx New York 10461 —
University of North Carolina Chapel Hill North Carolina 25799 —
Atrium Health Charlotte North Carolina 28207 —
Duke University Durham North Carolina 27705 —
MetroHealth Cleveland Ohio 44109 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Temple University Philadelphia Pennsylvania 19122 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02995733, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 19, 2023 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02995733 live on ClinicalTrials.gov.

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