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A randomized, open-label, pragmatic study to assess reliever-triggered inhaled corticosteroid in African American/Black and Hispanic/Latinx adults with asthma: Design and methods of the PREPARE trial.

Authors :
Israel E
Cardet JC
Carroll JK
Fuhlbrigge AL
Pace WD
Maher NE
She L
Rockhold FW
Fagan M
Forth VE
Hernandez PA
Manning BK
Rodriguez-Louis J
Shields JB
Coyne-Beasley T
Kaplan BM
Rand CS
Morales-Cosme W
Wechsler ME
Wisnivesky JP
White M
Yawn BP
McKee MD
Busse PJ
Kaelber DC
Nazario S
Hernandez ML
Apter AJ
Chang KL
Pinto-Plata V
Stranges PM
Hurley LP
Trevor J
Casale TB
Chupp G
Riley IL
Shenoy K
Pasarica M
Calderon-Candelario RA
Tapp H
Baydur A
Source :
Contemporary clinical trials [Contemp Clin Trials] 2021 Feb; Vol. 101, pp. 106246. Date of Electronic Publication: 2020 Dec 11.
Publication Year :
2021

Abstract

Background: Asthma prevalence, morbidity, and mortality disproportionately impact African American/Black (AA/B) and Hispanic/Latinx (H/L) communities. Adherence to daily inhaled corticosteroid (ICS), recommended by asthma guidelines in all but the mildest cases of asthma, is generally poor. As-needed ICS has shown promise as a patient-empowering asthma management strategy, but it has not been rigorously studied in AA/B or H/L patients or in a real-world setting. Design and Aim The PeRson EmPowered Asthma RElief (PREPARE) Study is a randomized, open-label, pragmatic study which aims to assess whether a patient-guided, reliever-triggered ICS strategy called PARTICS (Patient-Activated Reliever-Triggered Inhaled CorticoSteroid) can improve asthma outcomes in AA/B and H/L adult patient populations. In designing and implementing the study, the PREPARE research team has relied heavily on advice from AA/B and H/L Patient Partners and other stakeholders. Methods PREPARE is enrolling 1200 adult participants (600 AA/Bs, 600H/Ls) with asthma. Participants are randomized to PARTICS + Usual Care (intervention) versus Usual Care (control). Following a single in-person enrollment visit, participants complete monthly questionnaires for 15 months. The primary endpoint is annualized asthma exacerbation rate. Secondary endpoints include asthma control; preference-based quality of life; and days lost from work, school, or usual activities. Discussion The PREPARE study features a pragmatic design allowing for the real-world assessment of a patient-centered, reliever-triggered ICS strategy in AA/B and H/L patients. Outcomes of this study have the potential to offer powerful evidence supporting PARTICS as an effective asthma management strategy in patient populations that suffer disproportionately from asthma morbidity and mortality.<br /> (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1559-2030
Volume :
101
Database :
MEDLINE
Journal :
Contemporary clinical trials
Publication Type :
Academic Journal
Accession number :
33316456
Full Text :
https://doi.org/10.1016/j.cct.2020.106246