Strength Training in Duchenne Muscular Dystrophy
| Status: | Completed |
|---|---|
| Conditions: | Neurology, Orthopedic |
| Therapuetic Areas: | Neurology, Orthopedics / Podiatry |
| Healthy: | No |
| Age Range: | 7 - 10 |
| Updated: | 3/8/2019 |
| Start Date: | May 30, 2015 |
| End Date: | October 8, 2018 |
Development of a Strength Training Protocol in Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is a debilitating neuromuscular disease that causes muscle
breakdown, weakness, and eventual death. Over the last 40 years parents have received little
guidance on the potential of exercise as a therapeutic strategy to maintain muscle function.
It is well known that high intensity exercise and eccentric contractions can result in muscle
damage in dystrophic muscle, yet the absence of muscle loading will conversely result in
muscle wasting. Recent research in rodent models and milder forms of muscular dystrophy
supports earlier studies that resistance exercise may have beneficial effects for maintenance
of muscle mass in dystrophic muscle. However, careful and systematic investigation into the
safety and feasibility of resistance exercise is needed to consider its implementation in
boys with DMD.
The goal of this project is to assess the safety and feasibility of a home based mild to
moderate-intensity strengthening exercise program in boys with Duchenne muscular dystrophy
(DMD). Evidence from milder forms of muscular dystrophy and mouse models of DMD suggests that
strengthening exercise may be beneficial for these children, but this area has not been
adequately explored using human subjects. The results of this study should provide
information to assist in the development of scientifically based recommendations concerning
optimal exercise parameters for patients with DMD.
breakdown, weakness, and eventual death. Over the last 40 years parents have received little
guidance on the potential of exercise as a therapeutic strategy to maintain muscle function.
It is well known that high intensity exercise and eccentric contractions can result in muscle
damage in dystrophic muscle, yet the absence of muscle loading will conversely result in
muscle wasting. Recent research in rodent models and milder forms of muscular dystrophy
supports earlier studies that resistance exercise may have beneficial effects for maintenance
of muscle mass in dystrophic muscle. However, careful and systematic investigation into the
safety and feasibility of resistance exercise is needed to consider its implementation in
boys with DMD.
The goal of this project is to assess the safety and feasibility of a home based mild to
moderate-intensity strengthening exercise program in boys with Duchenne muscular dystrophy
(DMD). Evidence from milder forms of muscular dystrophy and mouse models of DMD suggests that
strengthening exercise may be beneficial for these children, but this area has not been
adequately explored using human subjects. The results of this study should provide
information to assist in the development of scientifically based recommendations concerning
optimal exercise parameters for patients with DMD.
The overall objective of this pilot study is to assess whether a mild to moderate-intensity
strengthening exercise program can be safely implemented in boys with DMD. In Aim 1, the
investigators will determine the dose response and safety of mild to moderate-intensity
isometric resistance exercise in children with DMD. Twelve ambulatory boys with DMD will
participate in an isometric exercise dosing protocol, in which the load is progressively
increased. In this early proof of concept pilot study, two large muscle groups will be
studied: the knee extensors and the knee flexors. T2 weighted magnetic resonance imaging
(MRI) of the thigh muscles will be used to monitor evidence of muscle damage at each
intensity level and determine a safe exercise range. Other safety measures will include a
verbal pain rating scale, clinical examination, and serum creatine kinase (CK) levels. In Aim
2, the investigators will implement a pilot intervention study to examine the feasibility and
safety of a 12 week in-home isometric strengthening program in children with DMD. In this
study, 20 boys with DMD will be randomized to either an exercise group or a control group.
Ten boys with DMD randomized to the exercise group will complete a progressive exercise
program using the parameters and dose identified in Aim 1. Assessment of strength and safety
will be performed at regular time intervals throughout the study. Ten boys with DMD
randomized to not participate in an exercise intervention will be tested at similar time
intervals and serve as controls. The data from this pilot study will serve to perform the
power analysis needed to design an appropriately powered clinical intervention study.
strengthening exercise program can be safely implemented in boys with DMD. In Aim 1, the
investigators will determine the dose response and safety of mild to moderate-intensity
isometric resistance exercise in children with DMD. Twelve ambulatory boys with DMD will
participate in an isometric exercise dosing protocol, in which the load is progressively
increased. In this early proof of concept pilot study, two large muscle groups will be
studied: the knee extensors and the knee flexors. T2 weighted magnetic resonance imaging
(MRI) of the thigh muscles will be used to monitor evidence of muscle damage at each
intensity level and determine a safe exercise range. Other safety measures will include a
verbal pain rating scale, clinical examination, and serum creatine kinase (CK) levels. In Aim
2, the investigators will implement a pilot intervention study to examine the feasibility and
safety of a 12 week in-home isometric strengthening program in children with DMD. In this
study, 20 boys with DMD will be randomized to either an exercise group or a control group.
Ten boys with DMD randomized to the exercise group will complete a progressive exercise
program using the parameters and dose identified in Aim 1. Assessment of strength and safety
will be performed at regular time intervals throughout the study. Ten boys with DMD
randomized to not participate in an exercise intervention will be tested at similar time
intervals and serve as controls. The data from this pilot study will serve to perform the
power analysis needed to design an appropriately powered clinical intervention study.
Inclusion Criteria:
- Diagnosis of DMD confirmed by
1. clinical history with features before the age of five
2. physical examination
3. elevated serum creatine kinase level
4. absence of dystrophin expression, as determined by immunostain or Western blot
(<2%) and/or DNA confirmation of dystrophin mutation.
- Age 7 to 10.5 years: a lower age limit of 7 years was selected, since in our
experience children younger than 7 years are likely unable to cooperate and comply
with all of the exercise measures as needed. An upper age limit of 10.5 years has been
set as boys with DMD tend to reach a rapid progression into a late ambulatory phase
soon after this age.
- Ambulatory at the time of the first visit, defined as the ability to walk for at least
100 m without an external assistive device and able to climb four stairs.
- Currently using corticosteroids (prednisone or deflazacort) as prescribed by a
physician.
Exclusion Criteria:
- Contraindication to an MR examination (e.g. aneurysm clip, severe claustrophobia,
magnetic implants)
- Presence of a condition in control subjects or a secondary condition in boys with DMD
that impacts muscle function or muscle metabolism (e.g. myasthenia gravis, endocrine
disorder, mitochondrial disease)
- Secondary condition leading to developmental delay or impaired motor control (e.g.
cerebral palsy)
- Secondary condition that impacts muscle function or muscle metabolism (e.g. myasthenia
gravis, endocrine disorder, mitochondrial disease)
- Unstable medical condition (e.g. uncontrolled seizure disorder)
- Behavioral problems causing an inability to cooperate during testing
We found this trial at
1
site
University of Florida The University of Florida (UF) is a major, public, comprehensive, land-grant, research...
Click here to add this to my saved trials
