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.

Figures

Figure 1.
Figure 1.
Custom adapters to allow inspiratory muscle training using expiratory-type RMT devices including the Threshold PEP (top) and EMST 150 (bottom). Includes one-way gas valve to allow expiration without resistance before initiating inspiratory repetitions.
Figure 2.
Figure 2.
RMT Monitor shown interfacing with the EMST 150 device (covered in heat-shrink tubing) for expiratory muscle training. The device allows automated data collection, provides user feedback after each repetition, and enhances control over RMT dose.
Figure 3.. Study Overview.
Figure 3.. Study Overview.
PSG = polysmnography, RMT Tx = on-site RMT or sham therapy visits, Phone Check = RMT clinician telephone check.

Source: PubMed

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