Benefits and Tolerance of Exercise in Patients With Generalized and Stabilized Myasthenia Gravis (MGEX)
Primary Purpose
Myasthenia Gravis
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Physical exercise programme using a rowing machine
Sponsored by
About this trial
This is an interventional treatment trial for Myasthenia Gravis focused on measuring Myasthenia gravis, physical exercise, quality of life, muscular performance, fatigability
Eligibility Criteria
Inclusion Criteria:
Patient with generalized MG of stage II or III according to the MGFA classification, stabilized for at least 6 months. Criteria for MG are either
- positive dosage of ant-RACh or MuSK auto-antibodies;
- If absent, myasthenic symptoms decrement> 10% in EMNG and test the positive prostigmine
- Patient ≥ 18 and ≤ 70 years old
- Patient having an health insurance
- Informed written consent
Exclusion Criteria:
- Patients under particular protection
- Enrolment in another biomedical research in the last 3 months;
Patients for whom physical practice is contra-indicated because of :
- Unstable coronary Syndrome or myocardial infarction within the past 3 months
- Heart failure with systolic ejection fraction < 50 %
- Respiratory failure defined by a vital capacity (CV) < 70 %
- Stroke
- Other neuromuscular pathology
- Disabling Rheumatologic disease (> 80 % disability according to the Barthel scale)
- Chronic Pain or disabling orthopaedic conditions
- Hospitalization in the last 3 months for a serious medical or surgical condition
- Anemia (hematocrit < 30%)
- MGFA grade I, grade IV or V
- Severe cognitive impairment
- MGQOL-15 below 15/60
Sites / Locations
- ICU and medical surgery department, Raymond Poincaré Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Physical exercise arm
Control arm
Arm Description
Arm with physical exercise on rowing machine between M3 and M6
Arm with standard medical care without additional physical exercise
Outcomes
Primary Outcome Measures
Change in the quality of life between M3 and M6 by MGQOL score
Secondary Outcome Measures
Muscular strength
Muscular strength (before exercise period, after exercise period and 3 months after)
Frequency of MG exacerbations
Frequency and severity of cardiovascular side-effects
Cumulative dose of steroids within the 3 months of the exercise programme
Doses of anticholinesterasic and steroids at 3, 6 and 9 months
Psychological status (STAI, BECK, MINI et SEI scales) at 3, 6 and 9 months
Plasma levels of pro- and anti-inflammatory cytokines at 9 months
Muscular fatigability
fatigability (before exercise period, after exercise period and 3 months after)
Muscular endurance
muscular endurance (before exercise period, after exercise period and 3 months after)
Severity of MG exacerbations
Frequency and severity of respiratory side-effects
Full Information
NCT ID
NCT02066519
First Posted
January 13, 2014
Last Updated
August 10, 2018
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT02066519
Brief Title
Benefits and Tolerance of Exercise in Patients With Generalized and Stabilized Myasthenia Gravis
Acronym
MGEX
Official Title
Benefits and Tolerance of Exercise in Patients With Generalized and Stabilized Myasthenia Gravis
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
October 2014 (Actual)
Primary Completion Date
January 10, 2018 (Actual)
Study Completion Date
April 6, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to demonstrate that a 3 months physical exercise programme improves the Quality of Life of patients with generalized Myasthenia Gravis (MG) stabilized since at least 6 months under prednisone and/or azathioprine.
Detailed Description
Three centers randomized simple blind clinical trial whose objective is to assess the efficacy on QoL improvement, and the tolerance of physical exercise over a period of 3 months in patients with generalized MG who have been stabilized since at least 6 months.
During the 3 months pre-inclusion phase, the characteristics of MG will be collected. Physical activity and performance will be assessed monthly.
MGQOL15 will be assessed at inclusion.
Patients will be randomized in either intervention arm or control arm.
The intervention arm will consist of three sessions exercise per week during three months. The daily exercise will be performed on a rowing machine that will be adapted to the patient's own physical ability.
Physical activity will be measured with the help of an actimeter.
Once a month, MG evolution and tolerance to exercise will be assessed and MG treatment dose will be collected.
Exercise will be interrupted in case of MG exacerbation.
Quality of life and psychological status will be assessed at 3, 6 and 9 months.
Plasma levels of pro and anti-inflammatory cytokines will be measured at 3, 6 and 9 months in order to assess the effects of exercise on immune response.
Patients enrolled in the control arm will benefit from the same follow-up but will not have exercise.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myasthenia Gravis
Keywords
Myasthenia gravis, physical exercise, quality of life, muscular performance, fatigability
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
45 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Physical exercise arm
Arm Type
Experimental
Arm Description
Arm with physical exercise on rowing machine between M3 and M6
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Arm with standard medical care without additional physical exercise
Intervention Type
Behavioral
Intervention Name(s)
Physical exercise programme using a rowing machine
Intervention Description
3 sessions per week of individualized physical training using a rowing machine during 3 months.
Primary Outcome Measure Information:
Title
Change in the quality of life between M3 and M6 by MGQOL score
Time Frame
M3 and M6
Secondary Outcome Measure Information:
Title
Muscular strength
Description
Muscular strength (before exercise period, after exercise period and 3 months after)
Time Frame
M3, M6 and M9
Title
Frequency of MG exacerbations
Time Frame
6 MONTHS
Title
Frequency and severity of cardiovascular side-effects
Time Frame
6 MONTHS
Title
Cumulative dose of steroids within the 3 months of the exercise programme
Time Frame
6 MONTHS
Title
Doses of anticholinesterasic and steroids at 3, 6 and 9 months
Time Frame
M3, M6 and M9
Title
Psychological status (STAI, BECK, MINI et SEI scales) at 3, 6 and 9 months
Time Frame
M3, M6 and M9
Title
Plasma levels of pro- and anti-inflammatory cytokines at 9 months
Time Frame
M9
Title
Muscular fatigability
Description
fatigability (before exercise period, after exercise period and 3 months after)
Time Frame
M3, M6 and M9
Title
Muscular endurance
Description
muscular endurance (before exercise period, after exercise period and 3 months after)
Time Frame
M3, M6 and M9
Title
Severity of MG exacerbations
Time Frame
6 MONTHS
Title
Frequency and severity of respiratory side-effects
Time Frame
6 MONTHS
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient with generalized MG of stage II or III according to the MGFA classification, stabilized for at least 6 months. Criteria for MG are either
positive dosage of ant-RACh or MuSK auto-antibodies;
If absent, myasthenic symptoms decrement> 10% in EMNG and test the positive prostigmine
Patient ≥ 18 and ≤ 70 years old
Patient having an health insurance
Informed written consent
Exclusion Criteria:
Patients under particular protection
Enrolment in another biomedical research in the last 3 months;
Patients for whom physical practice is contra-indicated because of :
Unstable coronary Syndrome or myocardial infarction within the past 3 months
Heart failure with systolic ejection fraction < 50 %
Respiratory failure defined by a vital capacity (CV) < 70 %
Stroke
Other neuromuscular pathology
Disabling Rheumatologic disease (> 80 % disability according to the Barthel scale)
Chronic Pain or disabling orthopaedic conditions
Hospitalization in the last 3 months for a serious medical or surgical condition
Anemia (hematocrit < 30%)
MGFA grade I, grade IV or V
Severe cognitive impairment
MGQOL-15 below 15/60
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tarek SHARSHAR, MD, PhD
Organizational Affiliation
ICU and medical surgery Service, Raymond Poincaré Hospital, 92380 Garches, France
Official's Role
Principal Investigator
Facility Information:
Facility Name
ICU and medical surgery department, Raymond Poincaré Hospital
City
Garches
State/Province
Hauts-de-Seine
ZIP/Postal Code
92380
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
34304969
Citation
Birnbaum S, Porcher R, Portero P, Clair B, Demeret S, Eymard B, Gargiulo M, Louet E, Berrih-Aknin S, Le Panse R, Aegerter P, Hogrel JY, Sharshar T; MGEX Study Group. Home-based exercise in autoimmune myasthenia gravis: A randomized controlled trial. Neuromuscul Disord. 2021 Aug;31(8):726-735. doi: 10.1016/j.nmd.2021.05.002. Epub 2021 May 27.
Results Reference
derived
PubMed Identifier
29347991
Citation
Birnbaum S, Hogrel JY, Porcher R, Portero P, Clair B, Eymard B, Demeret S, Bassez G, Gargiulo M, Louet E, Berrih-Aknin S, Jobic A, Aegerter P, Thoumie P, Sharshar T; MGEX Study Group. The benefits and tolerance of exercise in myasthenia gravis (MGEX): study protocol for a randomised controlled trial. Trials. 2018 Jan 18;19(1):49. doi: 10.1186/s13063-017-2433-2.
Results Reference
derived
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Benefits and Tolerance of Exercise in Patients With Generalized and Stabilized Myasthenia Gravis
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