Rheumatoid ArthritisEECRANCT02320188
Eccentric Exercise and Cachexia in Rheumatoid Arthritis
A study testing Eccentric exercise and Concentric exercise in people with Rheumatoid Arthritis, run by University Hospital, Clermont-Ferrand at 1 site in France.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 40 to 66 years, women only
- Conditions the study is for
- Rheumatoid Arthritis
- What is being tested?
- Eccentric exercise and Concentric exercise
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 48 participants
- Where
- 1 siteFrance
- Study dates
- Dec 2014to 28 Feb 2019
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 66 years
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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
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- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
France1 site, 1 recruiting
- Recruiting
CHU Clermont-Ferrand
Clermont-Ferrand, 63003
Patrick LACARIN, 04 73 75 11 95, placarin@chu-clermontferrand.fr
About this study
Official title: Effect of Eccentric Exercise Training in Rheumatoid Cachexia
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.
Read the 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.
- Conditions
- Rheumatoid Arthritis
- Being tested
- Eccentric exercise, Concentric exercise
- Keywords
- modification of treatment planned, Exercise
- Medical subject headings
- Arthritis, Rheumatoid, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Eccentric exerciseOther
This study aimed to determine the muscle effects of ECC training, with the primary outcome being the knee extensor strength gain at 3 months.
Concentric exerciseOther
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.
| Study group | Role | What they receive |
|---|---|---|
| Eccentric exercise | Experimental | Thirty sessions of Eccentric training in twelve weeks. Average of two sessions per week without spacing higher than eight days between two sessions. Receives: Other: Eccentric exercise |
| Concentric exercise | Experimental | Thirty sessions of Concentric training in twelve weeks. Average of three sessions per week without spacing higher than eight days between two sessions. Receives: Other: Concentric exercise |
| No training (control) | No intervention | Usual activities. No further training during the observation period |
What is being measured
The primary outcome is the main question the study is designed to answer.
Isometric knee extensor strength gain measured by an isokinetic dynamometer
Measured: at 3 months
Secondary outcomes (3)
improvement in muscle mass
quadriceps muscle volume
Measured: Up to 30 days before the beginning of the training, after 3 and 6 months
improvement in fonctional status
Body composition : Lean body mass, Appendicular lean mass
Measured: At the beginning of the training, after 3 and 6 months
improvement in cardiovascular risk
Cardiovascular risk : arterial compliance
Measured: At the beginning of the training, after 3 and 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Dec 2014 (estimated)
- Study startDec 2014
- Primary completion28 Feb 2019 (estimated)
- Study completion28 Feb 2019 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Rheumatoid ArthritisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 48 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Clermont-Ferrand
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Anne TOURNADRE, Principal investigator, University Hospital, Clermont-Ferrand
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02320188
- Sponsor's protocol ID
- CHU-0215
- Other IDs
- 2013-A01789-36
- Acronym
- EECRA
- Status last verified
- Feb 2019
- First submitted
- 16 Dec 2014
- Last updated
- 4 Feb 2019
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Feb 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Eccentric Exercise Training in Rheumatoid Cachexia
- ClinicalTrials.gov ID
- NCT02320188
- Acronym / sponsor ID
- EECRA / CHU-0215
- Conditions
- Rheumatoid Arthritis
- Keywords
- modification of treatment planned, Exercise
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 48 participants (estimated)
- Lead sponsor
- University Hospital, Clermont-FerrandUniversity, hospital or other
- Study start
- Dec 2014
- Primary completion
- 28 Feb 2019 (estimated)
- Study completion
- 28 Feb 2019 (estimated)
- First posted
- 19 Dec 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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 design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Eccentric exercise | Experimental | Other: Eccentric exerciseThirty sessions of Eccentric training in twelve weeks. Average of two sessions per week without spacing higher than eight days between two sessions. |
| Concentric exercise | Experimental | Other: Concentric exerciseThirty sessions of Concentric training in twelve weeks. Average of three sessions per week without spacing higher than eight days between two sessions. |
| No training (control) | No intervention | –Usual activities. No further training during the observation period |
Who may qualify
- Ages
- 40 to 66 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- 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
Key exclusion criteria (8 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Eccentric exerciseThis study aimed to determine the muscle effects of ECC training, with the primary outcome being the knee extensor strength gain at 3 months. | Other | Eccentric exercise |
| Concentric exerciseThe 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. | Other | Concentric exercise |
Primary outcome
Isometric knee extensor strength gain measured by an isokinetic dynamometer
Time frame: at 3 months
3 secondary outcomes
improvement in muscle mass
Time frame: 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
improvement in cardiovascular risk
Time frame: At the beginning of the training, after 3 and 6 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Feb 2019.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Anne TOURNADRE principal investigator
University Hospital, Clermont-Ferrand
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Eccentric exercise and Concentric exercise in people with Rheumatoid Arthritis, run by University Hospital, Clermont-Ferrand at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 4 Feb 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Patrick LACARIN (04 73 75 11 95, placarin@chu-clermontferrand.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Isometric knee extensor strength gain measured by an isokinetic dynamometer (time frame: at 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Feb 2019.