Holter of Movement in Patients With Amyotrophic Lateral Sclerosis.
Recruiting now
Conditions studied: Amyotrophic Lateral Sclerosis
In brief
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.
Key facts
- Study ID
- NCT06228001
- Run by
- Centre Hospitalier Universitaire de Liege
- People needed
- 30
- Starts
- 2023-05-01
- Expected to finish
- 2028-01-01
- Last updated by the study team
- 2025-05-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- Patients with excessive cognitive disorders, limiting the understanding of task or with apparent communication difficulties hindering data collection.
- Any other previous or present pathology having an impact on motor function.
- Recent surgery or trauma (less than 6 months) in the upper or lower limbs.
- Prior neurological, endocrine, infectious, allergic, or chronic or acute inflammatory pathology in the three weeks preceding inclusion.
- Patients participating in an interventional clinical trial.
Where it is running
- Katholieke Universiteit Leuven — Leuven, Belgium (enrolling)
- Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle — Liège, Belgium (enrolling)
- Galaa Military Medical Complex — Cairo, Egypt
Full record on ClinicalTrials.gov
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