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Updated: Aug 20, 2025

A Protocol for Comprehensive Assessment of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis ALS
Published on: February 21, 2011
Physical therapy for the management of motor symptoms in amyotrophic lateral sclerosis: protocol for a systematic
Stephano Tomaz Silva1, Aline Alves de Souza2, Karen Pondofe2
1Department of Physical Therapy, Federal University of Rio Grande do Norte, Natal, Brazil stephano.tomaz@gmail.com.
Introduction:
The prescription of an intervention plan can be challenging for the physical therapist, considering clinical phenotypes, individual prognosis and the rapid, progressive and deteriorating nature of amyotrophic lateral sclerosis (ALS). In this context, therapeutic exercises (eg, resistance and aerobic exercises) for patients with ALS remain controversial and may influence the treatment plan. Therefore, this review aims to critically assess whether physical therapy interventions are effective for improving functional capacity, quality of life and fatigue of individuals with ALS.
Methods And Analysis:
Studies will be selected according to eligibility criteria, and language, geographical area or publication date will not be restricted. Four databases will be used: MEDLINE, EMBASE, Cochrane Library (CENTRAL) and Physiotherapy Evidence Database (PEDro). Searches will also be conducted on ClinicalTrials.gov and references from included studies. We plan to conduct the searches between October and December 2022. Two independent authors will examine titles and abstracts and exclude irrelevant studies and duplicates. We will assess the quality of studies and quality of evidence, and disagreements will be resolved with a third researcher. The findings will be presented in the text and tables; if possible, we will perform meta-analyses.
Ethics And Dissemination:
No ethical approval is required because this study does not involve human beings. We will publish our findings in peer-reviewed journals.
Prospero Registration Number:
CRD42021251350.
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