Abstract
Introduction: The aim of this study was to assess the prevalence of participation restrictions in ambulatory patients with amyotrophic lateral sclerosis (ALS) and to identify physical and psychological contributory factors. Methods: In this cross-sectional study, self-reported participation restrictions of 72 ambulatory ALS patients were assessed using the social health status dimension (SIPSOC) of the Sickness Impact Profile (SIP-68). Associations between SIPSOC and physical functioning, psychological factors, and demographic factors were analyzed using hierarchical regression analyses. Results: Ninety-two percent of the patients reported participation restrictions; 54.9% could be explained by physical functioning; psychological factors accounted for 8.1% of the variance. Lung capacity, functional mobility, fatigue, and helplessness were independently associated with participation restrictions. Conclusions: Ambulatory ALS patients have participation restrictions, which may be influenced if early ALS care is directed toward lung capacity, functional mobility, fatigue, and feelings of helplessness. Muscle Nerve 56: 912–918, 2017.
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Van Groenestijn, A. C., Schröder, C. D., Kruitwagen-Van Reenen, E. T., Van Den Berg, L. H., & Visser-Meily, J. M. A. (2017). Participation restrictions in ambulatory amyotrophic lateral sclerosis patients: Physical and psychological factors. Muscle and Nerve, 56(5), 912–918. https://doi.org/10.1002/mus.25574
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