Respiratory muscle training (RMT) in late-onset Pompe disease (LOPD): A protocol for a sham-controlled clinical trial
Harrison N Jones, Maragatha Kuchibhatla, Kelly D Crisp, Lisa D Hobson Webb, Laura Case, Milisa T Batten, Jill A Marcus, Richard M Kravitz, Priya S Kishnani, Harrison N Jones, Maragatha Kuchibhatla, Kelly D Crisp, Lisa D Hobson Webb, Laura Case, Milisa T Batten, Jill A Marcus, Richard M Kravitz, Priya S Kishnani
Abstract
Introduction:: Morbidity and mortality in adults with late-onset Pompe disease (LOPD) results primarily from persistent progressive respiratory muscle weakness despite treatment with enzyme replacement therapy (ERT). To address this need, we have developed a 12-week respiratory muscle training (RMT) program that provides calibrated, individualized, and progressive pressure-threshold resistance against inspiration and expiration. Our previous results suggest that our RMT regimen is safe, well-tolerated, and results in large increases in respiratory muscle strength. We now conduct an exploratory double-blind, randomized control trial (RCT) to determine: 1) utility and feasibility of sham-RMT as a control condition, 2) the clinically meaningful outcome measures for inclusion in a future efficacy trial. This manuscript provides comprehensive information regarding the design and methods used in our trial and will aid in the reporting and interpretation of our future findings.
Methods:: Twenty-eight adults with LOPD will be randomized (1:1) in blocks of 4 to RMT (treatment) or sham-RMT (control). Assessments will be conducted at pretest, posttest, 3-months detraining, and 6-months detraining. The primary outcome is maximum inspiratory pressure (MIP). Secondary outcomes include maximum expiratory pressure (MEP), 6-minute walk test (6MWT), Gait, Stairs, Gowers, and Chair test (GSGC), peak cough flow (PCF), and patient-reported life activity/social participation (Rasch-built Pompe-specific Activity scale [R-Pact]). Exploratory outcomes include quantitative measures from polysomnography; patient reported measures of fatigue, daytime sleepiness, and sleep quality; and ultrasound measures of diaphragm thickness. This research will use a novel tool to provide automated data collection and user feedback, and improve control over dose.
Ethics and dissemination:: The results of this clinical trial will be promptly analyzed and submitted for publication. Results will also be made available on clinicaltrials.gov.
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Trial registration: ClinicalTrials.gov NCT02801539.
Keywords: Late-onset Pompe disease; Maximum expiratory pressure; Maximum inspiratory pressure; Pompe disease; Randomized control trial; Respiratory muscle training.
Copyright © 2019 Elsevier Inc. All rights reserved.
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Source: PubMed