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Clinical Trials/NCT01167283
NCT01167283
Completed
Not Applicable

Effect of Electromyostimulation in Severe Chronic Obstructive Pulmonary Disease

Institut National de la Santé Et de la Recherche Médicale, France0 sites15 target enrollmentJuly 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Enrollment
15
Primary Endpoint
Fiber-type distribution
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

This study was designed to test the following hypothesis:

To investigate whether COPD muscles can respond to stimuli in terms of changes in fiber-type distribution.

Detailed Description

Background: Muscle dysfunction is a major problem in chronic obstructive pulmonary disease (COPD). It is characterized by muscle fiber-type redistribution and oxidative stress. Classical training does not improve these features. Objectives: To investigate whether electrostimulation program following exacerbation can modify muscle structure and function in COPD patients. Method: We propose to conduct a controlled and randomized clinical trial comparing the efficacy of muscle electrostimulation training of the lower limbs to sham training in 15 patients with COPD. Patients are included in either 6 weeks of electrostimulation training (active treatment group) or 6 weeks of sham electrostimulation. Primary outcomes were changes in muscle structure, muscle oxidative stress and their relationship with quadriceps force and exercise tolerance.

Registry
clinicaltrials.gov
Start Date
July 2006
End Date
April 2010
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France

Eligibility Criteria

Inclusion Criteria

  • COPD patients during or after exacerbation

Exclusion Criteria

  • Comorbidities that could limit exercise training
  • Obesity (body mass index \[BMI\] \> 30 kg/m²)
  • Neuromuscular disease
  • Pacemaker implantation

Outcomes

Primary Outcomes

Fiber-type distribution

Time Frame: 6 to 8 weeks

Typology was evaluated by immunohistochemistry

Secondary Outcomes

  • Change in the strength of the quadriceps over the 6-week electrostimulation program(6 to 8 weeks)

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