Observational Study to Observe Variations of Gait Parameters in Patients With Neuromuscular Diseases
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 75 years old?
Where in Olaszország
- Bosisio Parini · Scientific Institute IRCCS E. Medea - Sede di Bosisio PariniTaking people
- Conegliano · Scientific Institute IRCCS E. Medea - Polo di ConeglianoToborzás még nem indult
The registry text, word for word
Observational Study for the Identification of Fatigue and Gait Biomarkers in Populations With Neuromuscular Pathologies in the Clinical Context and Daily Life
This study has the general objective of observing walking parameters during a clinical test to objectively estimate fatigue in patients with neuromuscular diseases. Furthermore, the investigators want to evaluate the feasibility of collecting physical activity in daily life conditions during a one-week monitoring period using a wearable sensor.
Inclusion: Ambulant adult patients with genetic diagnosis of muscular dystrophy/myopathy (dystrophinopathies, muscular dystrophies and congenital and non-congenital myopathies), of spinal muscular atrophy (SMA) and with molecular diagnosis of Charcot-Marie Tooth 1 or 2; independent walking, even with assistance.
Exclusion: Dilated or ischemic heart disease with moderate impairment; Chronic respiratory failure: forced vital capacity (FVC) < 40%; more than 5% of nocturnal time spent with peripheral oxygen saturation levels < 90.