Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07450690

Exercise Training Effects on Muscle Function in Adults With Mitochondrial Myopathy

Led by University of Copenhagen · Updated on 2026-03-05

22

Participants Needed

1

Research Sites

250 weeks

Total Duration

On this page

Sponsors

U

University of Copenhagen

Lead Sponsor

R

Rigshospitalet, Denmark

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to learn how exercise training affects molecular processes in skeletal muscle in adults with mitochondrial myopathy, compared with healthy adults. The main questions it aims to answer are: * How does exercise training affect mitochondrial activity and energy production pathways in skeletal muscle in people with mitochondrial myopathy? * How does exercise training affect molecular signals related to muscle growth, stress responses, and muscle-nerve communication in people with mitochondrial myopathy? Researchers will compare the trained leg to the untrained leg within the same participant, and also compare responses between participants with mitochondrial myopathy and healthy control participants, to see how molecular responses to exercise differ between groups. The participants will: * Complete a 3-4-week supervised exercise training program using one leg. * Undergo muscle biopsies from both the trained and untrained leg. * Complete basic muscle strength and physical function tests.

CONDITIONS

Official Title

Exercise Training Effects on Muscle Function in Adults With Mitochondrial Myopathy

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • For mitochondrial myopathy group: known mitochondrial DNA or nuclear DNA mutations
  • For healthy controls: age 18 years or older
Not Eligible

You will not qualify if you...

  • Medical conditions making participation unsafe or incomplete
  • Use of medications that interact with study outcomes
  • Pregnancy
  • Any other reason likely to prevent completing the study
  • For healthy controls: chronic medical conditions affecting outcomes
  • For healthy controls: frequent medication use

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Copenhagen, Dept of Biomedical Sciences

Copenhagen, Denmark, DK-2100

Actively Recruiting

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Research Team

T

Tue L Nielsen, MD

CONTACT

L

Lykke Sylow, Ass.prof

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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