Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease) Clinical Trials

Find Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease) Clinical Trials Near You

Continuous Measurement of Activity in Patients With Muscle Pathology and in Control Subjects

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Clinically defined or probable diagnosis of ALS according to El Escorial criteria revised with Awaji's electro-diagnostic algorithm.

• Over 18 years old.

• Signed informed consent

• If patient on Riluzole, the dosage should be stable for 1 month and continued throughout the study period.

Locations
Other Locations
Belgium
CHR Citadelle
RECRUITING
Liège
Contact Information
Primary
Laurie MEDARD
Laurie.Medard@citadelle.be
43218222
Time Frame
Start Date: 2020-09-25
Estimated Completion Date: 2026-12
Participants
Target number of participants: 45
Treatments
Experimental: Patient with ALS
Patient with amyotrophic lateral sclerosis
Sponsors
Leads: Centre Hospitalier Universitaire de Liege
Collaborators: SYSNAV, Centre Hospitalier Régional de la Citadelle

This content was sourced from clinicaltrials.gov