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Study identifier: NCT06708468 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Personalized Training for People With Rare Neuromuscular Disorders

Condition: Neuromuscular Diseases (NMD) · Charcot Marie Tooth Disease (CMT) · Facioscapulohumeral Muscular Dystrophy  ·  Sponsor: Oslo University Hospital

PhaseNA
Planned participants120
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

The goal of this study is to investigate the effects of personalized exercise treatment on dynamic balance and physical function in comparison with regular follow-up in adults with rare-neuromuscular disorders: Charcot-Marie-Tooth (CMT), Facioscapulohumeral Muscular Dystrophy (FSHD), and Myotonic Dystrophy Type 1 (DM1). The key objectives are: 1. To investigate if the intervention group experiences improvements in dynamic balance that are superior to the control group 2. To investigate if the intervention group experiences long-term improvements in dynamic balance that are superior to the control group during the follow-up 3. To investigate if improvements in dynamic balance are associated with improvements in physical activity, body composition, estimated motor units, metabolomics, muscle echnogenecity and volume, and other indicators of health and quality of life. This is a national study and will involve 120 individuals with rare-neuromuscular disorders from Norway's four health regions.

This description comes directly from the study's public registry record.

Talk to the study team

Kristin Ørstavik, MD, PhD  ·  +4792422126  ·  krorstav@ous-hf.no

Hanne L Fossmo, PhD stud  ·  +4793630606  ·  halufo@ous-hf.no

Always discuss trial participation with your own doctor first.

Locations (5)

Haukeland University HospitalBergen, NorwayNot Yet Recruiting
Helse Møre and Romsdal HF (Molde Hospital)Molde, NorwayNot Yet Recruiting
Namsos HospitalNamsos, NorwayNot Yet Recruiting
Oslo University HospitalOslo, NorwayRecruiting
University Hospital of North NorwayTromsø, NorwayRecruiting

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Source record: clinicaltrials.gov/study/NCT06708468