Aerobic Training in Patients With Congenital Myopathies

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Completed
CT.gov ID
NCT02020187
Collaborator
(none)
16
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2
14
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Study Details

Study Description

Brief Summary

Congenital myopathies are clinical and genetic heterogeneous disorders characterized by skeletal muscle weakness. Most patients experience muscle weakness and fatigue throughout their life. However, progression of symptoms is rare. There are no specific treatments for congenital myopathies. Training has been shown to benefit several other muscle diseases with weakness, but the defect in congenital myopathies involves contractile proteins of the sarcomere, why the effect of training is uncertain in these conditions. The investigators will therefore investigate the effect cycle-ergometer training for 30 minutes, three times weakly, for ten weeks in 15 patients with congenital myopathy. Another 5-10 congenital myopathy patients, who do not train, will serve as controls for the trained patients. The study starts and ends with a test day, where efficacy based on VO2max, performance in functional tests and a questionnaire will be assessed.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise on a cycle-ergometer
N/A

Detailed Description

10 weeks of cycle-ergometer training at home. Intensity at 70% of maximal VO2,max.

Study Design

Study Type:
Interventional
Actual Enrollment :
16 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Aerobic Training in Patients With Congenital Myopathies
Study Start Date :
Sep 1, 2013
Actual Primary Completion Date :
Nov 1, 2014
Actual Study Completion Date :
Nov 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Exercise

10 weeks of home training on a cycle-ergometer. Exercise 30 minutes every other day or at least three times a week.

Other: Exercise on a cycle-ergometer
Home training on an ergometer-cycle 30 minutes every other day or at least three times a week. Subject will exercise in a pulse interval corresponding to 70% of their maximal VO2.

No Intervention: Controls

Controls with diagnosed congenital myopathy. Subjects are tested two times on a cycle ergometer. There will be ten weeks between the tests. In between tests the subjects are living life as usual without any interventions.

Outcome Measures

Primary Outcome Measures

  1. Efficacy based on VO2,max [10 weeks]

    Difference in VO2,max from baseline to end of intervention.

Secondary Outcome Measures

  1. Level of Creatine Kinase [10 weeks]

    Marker for exercise-induced muscle damage. Taken week 0, 3 and 10.

  2. Intensity in maximal Watt [10 weeks]

    Changes in the maximal intensity (watt) from baseline VO2,max test to after the intervention.

  3. 6 minute walk test [10 weeks]

    Changes in the walking distance from baseline to after the intervention.

  4. SF-36 questionnaire [10 weeks]

    Changes in SF-36 questionnaire from baseline to after the intervention.

  5. A timed five-repetitions-sit-to-stand-test [10 weeks]

    Changes in time from baseline to after the intervention.

  6. A timed 14-step-stair-test [10 weeks]

    Changes in time from baseline to after the intervention.

  7. Dynamometry [10 weeks]

    Changes in external force production from baseline to after the intervention. Dynamometry measurements are done at hip flexion, dorsal foot flexion, plantar foot flexion, knee flexion, knee extension and elbow flexion.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Danish patients with gene verified congenital myopathy
Exclusion Criteria:
  • Patients who are to week to train at a cycle-ergometer for 10 weeks

  • Patients who have other health issues, which can disturb the interpretation of the efficacy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Neuromuscular Research Unit Copenhagen Denmark 2100

Sponsors and Collaborators

  • Rigshospitalet, Denmark

Investigators

  • Principal Investigator: Gitte H Pedersen, Bsc Medicine, Rigshospitalet, Denmark

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gitte Hedermann Pedersen, Medical student, Bsc, Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT02020187
Other Study ID Numbers:
  • H2-2013-066
First Posted:
Dec 24, 2013
Last Update Posted:
May 12, 2015
Last Verified:
May 1, 2015
Keywords provided by Gitte Hedermann Pedersen, Medical student, Bsc, Rigshospitalet, Denmark
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2015