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Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated May 20, 2025 (before its estimated March 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Notable Lead sponsor: Laurent Servais to Centre Hospitalier Universitaire de Liege
    • Site contacts updated at 1 of 8 sites
    v5
  2. Minor Study sites: 1 to 8v4
  3. Notable Enrollment target: 130 to 300
    • Interventions: ActiMyo (Device) to ActiMyo/Syde (Device)
    • Eligibility criteria expanded, about 156 words
    v3
  4. Minor Re-verified, no change to tracked fieldsv2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The objective of the ActiLiège Next study is to collect longitudinal data from patients and control subjects using a wearable magneto-inertial device. By collecting natural history data in various neuromuscular disorders (Duchenne Muscular Dystrophy, Fascioscapulohumeral Muscular Dystrophy, Myotonic Dystrophy 1, Charcot-Marie-Tooth, Centronuclear Myopathy, Congenital Muscular Dystrophy), we aim to validate digital outcome measures to continuously assess motor function in real-life.
Trial Details
NCT Number NCT05982119
Lead Sponsor Centre Hospitalier Universitaire de Liege
Collaborators: SYSNAV
Conditions
(from sponsor)
Duchenne Muscular Dystrophy, Fascioscapulohumeral Muscular Dystrophy, Myotonic Dystrophy 1, Charcot-Marie-Tooth, Centronuclear Myopathy, Congenital Muscular Dystrophy
Related terms Charcot-Marie-Tooth Disease, Muscular Dystrophy, Duchenne, Muscular Dystrophy, Facioscapulohumeral, Myopathies, Structural, Congenital, Myotonic Dystrophy
Enrollment 300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov