Targeting the Skeletal Muscle to Treat Metabolic Dysfunction-associated Steatotic Liver Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorCliniques universitaires Saint-Luc- Université Catholique de Louvain

About this trial

Muscle changes including myosteatosis are reported as highly prevalent in metabolic dysfunction-associated steatotic liver disease (MASLD). Recent studies highlighted a link between muscle fat content and liver disease severity. Conversely, MASLD histological remission though diet or metabolic surgeries is also linked to a decrease in muscle fat content. Therefore, skeletal muscle appears as a potential target to treat MASLD.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

confirmed MASLD at abdominal imaging

confirmed excessive muscle lipid content at imaging

stable weight

Disqualifiers

severe comorbidities including active malignancies, neuromuscular degenerative diseases

contraindications to physical activity

excessive alcohol consumption

Trial design

Design model

Parallel

Treatments tested in this trial

  • High-intensity interval training

    Other intervention

    High-intensity interval training

  • Moderate intensity exercise training

    Other intervention

    Moderate intensity exercise training

  • Low intensity exercise training

    Other intervention

    Low intensity exercise training

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: control groupActive comparator 1 intervention
Group B: moderate-intensity low interval training groupActive comparator 1 intervention
Group C: high-intensity interval trainingActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

the impact of physical activity on muscle and liver phenotypes

the investigators will assess at baseline and every four weeks till study completion the impact of intervention on liver phenotype assessed by transient elastography and muscle phenotype assessed by MRI

Time frame
every four weeks from baseline till study completion

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Lead sponsor

Concerted Research Action

Collaborator

Fonds National de la Recherche Scientifique

Collaborator