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Clinical Trial Summary

ActiSLA is a monocentric academic study. Patients with amyotrophic lateral sclerosis may be included on a voluntary basis. The investigators plan to include a group of approximately 20 patients with ALS. The investigators have planned to assess patient every three months for a year. On each visit, participants will undergo a clinical examination with MRC sum score and Ashworth scores. They will perform few tests ( 6-minutes walk test (6MWT), dynamometric measure, electromyography, Edinburgh Cognitive and Behavioural ALS Screen ) and will answer to some questionaires (dysphagia handicap scale, ALS-SFR-r). After each visit, participants will wear Actimyo for one month daily.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04882904
Study type Interventional
Source Centre Hospitalier Universitaire de Liege
Contact Laura Buscemi
Phone 43215584
Email Laura.Buscemi@chrcitadelle.be
Status Recruiting
Phase N/A
Start date September 25, 2020
Completion date January 2025

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