Pulmonary Disease, Chronic Obstructive Clinical Trial
Official title:
Eccentric Training as Novel Rehabilitation for COPD
Verified date | August 2018 |
Source | McGill University Health Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main purpose of this project is to establish the additional value of eccentric versus
concentric exercise to optimize muscle function in patients with severe COPD. With this pilot
project the investigators expect that an eccentric endurance training protocol adapted to
severe COPD patients will lead to gains in muscle strength, the primary outcome, and cellular
adaptation (muscle morphology and oxidative capacity, mitochondrial respiratory capacity)
when compared to a concentric training approach.
This information will be essential if the investigators want to design and power a randomized
clinical trial that will allow assessing effectiveness of this novel rehabilitation approach.
Status | Completed |
Enrollment | 24 |
Est. completion date | December 2012 |
Est. primary completion date | December 2012 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 40 Years to 80 Years |
Eligibility |
Inclusion Criteria: - male patients with severe COPD (FEV1/FVC < 0.70 and FEV1 = 50% predicted of normal) - Patients aged 40 to 80 years old in whom exercise is not contraindicated - Current and ex-smokers - Patients who do not require oxygen therapy Exclusion Criteria: - Patients presenting neurological or orthopedic problems, morbid obesity, acute medical condition or recent exacerbations (in the last four weeks) - Patients with recent or current participation in a rehabilitation program |
Country | Name | City | State |
---|---|---|---|
Canada | Montreal Chest Institute | Montreal | Quebec |
Lead Sponsor | Collaborator |
---|---|
McGill University Health Center |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Muscle strength | This outcome will be measured using an isokinetic dynamometer | At baseline, at the middle way point of the training program (5th to 7th week) and at the end of the 10-wk training program | |
Secondary | Muscle cellular adaptation | Muscle biopsy will include evaluation of cross-sectional area, fiber type, mitochondrial oxidative capacity, mitochondrial respiratory capacity, respiratory oxygen species and expression of genes involved in muscle atrophy and hypertrophy (Atrogin-1, MurF1, FoxO, MyoD, Myostatin) | At baseline and at the end of the training program | |
Secondary | Exercise capacity (maximal and submaximal) | At baseline, at the middle way point of the training program (5th to 7th week) and at the end of the 10-wk training program | ||
Secondary | Physical Activity | Physical activity levels will be measured by an accelerometer and by the CHAMPS questionnaire. | At baseline, at the middle way point of the training program (5th to 7th week) and at the end of the 10-wk training program | |
Secondary | Health-related quality of life (HRQL) | The HRQL will be measured by the Chronic Respiratory Questionnaire | At baseline, at the middle way point of the training program (5th to 7th week) and at the end of the 10-wk training program | |
Secondary | Muscle pain and creatine kinase(CK)levels | Muslce pain will be assessed in the beginning and in the end of each session and CK levels at baseline, after the fisrt week of training, midway through and the after the last week of training |
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