- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02320188
Eccentric Exercise and Cachexia in Rheumatoid Arthritis (EECRA)
Effect of Eccentric Exercise Training in Rheumatoid Cachexia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Rheumatoid arthritis (RA) is characterized by severe disability and metabolic changes leading to an increase in cardiovascular mortality compared with the general population. RA is an independent cardiovascular risk factor. In contrast to the general population, RA patients with low body mass index (BMI) had a significantly higher risk of cardiovascular death. Low BMI may indicate rheumatoid cachexia and may explain the excess cardiovascular risk and mortality. Cachexia is defined by is a loss of body cell mass, predominantly in skeletal muscle, associated with increased fat mass and often stable weight. Rheumatoid cachexia, not well recognized, is frequent, affecting two third of patients. Pathogenesis may include inflammatory cytokine production, physical inactivity, higher catabolism and reduced peripheral insulin action. Therapeutic strategy includes increasing physical activity and the treatment of disease itself. Studies have shown that regular progressive resistance strength training improves strength and pain in patients with well-controlled RA without exacerbating disease activity or joint pain. At comparable mechanical power output, eccentric (ECC ) exercises are characterised by lower metabolic demand than concentric (CON) exercises. ECC exercise is characterised not only by its low energy cost, but also by specific cardiocirculatory specificity. In patients with Parkinson's disease, compared to a conventional rehabilitation programme, ECC training better improved quadriceps muscle volume. In overweight and diabetic patients, ECC training improved resting energy expenditure and fat oxidation, blood lipid profile and insulin resistance compared to CON training. As in cancers, ECC training appears to be particularly suitable for patients with rheumatoid cachexia as it can maximize the functional and structural muscle responses with low energy cost populations.
This study aimed to determine the muscle effects of ECC training, with the primary outcome being the knee extensor strength gain at 3 months. Secondary outcomes are the improvement in muscle mass, functional status and cardiovascular risk. From patients who consented in ECC training group, muscle biopsy specimens from vastus lateralis will be obtained at baseline prior to the training period. Primary and secondary outcome criteria will be assessed at inclusion, at 3 months, and 6 months.
In total, 48 patients will need to be recruited. These patients will be randomly assigned to one of the 3 groups, with each group comprising 16 patients: group 1 with ECC training, group 2 with CONC training, group 3 with no training (control). The training program will consist in 30 sessions over 12 weeks.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Clermont-Ferrand, France, 63003
- Recruiting
- Chu Clermont-Ferrand
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age from 40 to 66 years old
- Diagnosis of rheumatoid arthritis according to ACR 1987 or ACR/EULAR 2010 criteria
- Activity of the disease measured by the DAS28 ≤3.2
- Stable for at least 3 months, no modification of treatment planned in the 3 months
- Steroids prednisone ≤ 0.1 mg/kg/day
- Steinbrocker functional classification for functional disability ≤ II
- The Questionnaire of Baecke for measurement of physical activity < 7.5
- Stable nutritional diet
- Patients resident in the area of "Grand Clermont"
- Clinical cachexia as defined by upper arm muscle area ≤75th percentile for age and sex
Exclusion Criteria:
- contraindication to exercise or to exercise stress test
- advanced hip or knee osteoarthritis
- Planned surgery of hip or knee
- Hip or knee arthroplasty preventing pedaling
- Chronic disease associated with cachexia
- Nutritional intervention
- Pregnancy
- For muscle biopsy: contraindication to local anesthesia, anticoagulation therapy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Eccentric exercise
Thirty sessions of Eccentric training in twelve weeks.
Average of two sessions per week without spacing higher than eight days between two sessions.
|
This study aimed to determine the muscle effects of ECC training, with the primary outcome being the knee extensor strength gain at 3 months.
|
|
Experimental: Concentric exercise
Thirty sessions of Concentric training in twelve weeks.
Average of three sessions per week without spacing higher than eight days between two sessions.
|
The purpose of the study is to determine in a randomized controlled trial (RCT), the efficacy of eccentric exercise training in restoring muscle mass and function in patients with rheumatoid cachexia.
|
|
No Intervention: No training (control)
Usual activities.
No further training during the observation period
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Isometric knee extensor strength gain measured by an isokinetic dynamometer
Time Frame: at 3 months
|
at 3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
improvement in muscle mass
Time Frame: Up to 30 days before the beginning of the training, after 3 and 6 months
|
quadriceps muscle volume
|
Up to 30 days before the beginning of the training, after 3 and 6 months
|
|
improvement in fonctional status
Time Frame: At the beginning of the training, after 3 and 6 months
|
Body composition : Lean body mass, Appendicular lean mass
|
At the beginning of the training, after 3 and 6 months
|
|
improvement in cardiovascular risk
Time Frame: At the beginning of the training, after 3 and 6 months
|
Cardiovascular risk : arterial compliance
|
At the beginning of the training, after 3 and 6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Anne Tournadre, University Hospital, Clermont-Ferrand
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHU-0215
- 2013-A01789-36 (Other Identifier: CHU de Clermont-Ferrand)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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