Actively Recruiting
Holter of Movement in Patients With Amyotrophic Lateral Sclerosis.
Led by Centre Hospitalier Universitaire de Liege · Updated on 2025-05-19
30
Participants Needed
3
Research Sites
243 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier Universitaire de Liege
Lead Sponsor
S
SYSNAV
Collaborating Sponsor
AI-Summary
What this Trial Is About
ActiALS is a multicentric academic study. Patients with amyotrophic lateral sclerosis (ALS) may be included on a voluntary basis. The investigators plan to include a group of approximately 30 patients with ALS. The investigators have planned to assess patient every three months for a year. After each visit, participants will wear Actimyo for one month daily.
CONDITIONS
Official Title
Holter of Movement in Patients With Amyotrophic Lateral Sclerosis.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinically defined or probable diagnosis of ALS according to El Escorial criteria revised with Awaji's electro-diagnostic algorithm
- Age 18 years or older
- Signed informed consent
- If on Riluzole, dosage must be stable for at least 1 month and continued throughout the study
You will not qualify if you...
- Excessive cognitive disorders limiting understanding or communication
- Any other previous or present pathology affecting motor function
- Recent surgery or trauma (less than 6 months) in upper or lower limbs
- Prior neurological, endocrine, infectious, allergic, or inflammatory conditions within 3 weeks before inclusion
- Participation in another interventional clinical trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Katholieke Universiteit Leuven
Leuven, Belgium, 1425
Actively Recruiting
2
Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle
Liège, Belgium, 4000
Actively Recruiting
3
Galaa Military Medical Complex
Cairo, Egypt
Active, Not Recruiting
Research Team
L
Laurie Medard
CONTACT
M
Margaux Poleur, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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