Parkinson Disease Clinical Trial
Official title:
High Force Resistance Training and Dopamine Replacement Effects on Hypokinesia in Parkinson Disease
Parkinson disease is a degenerative neurologic condition characterized by slowness of movement, tremor, and loss of balance control. It results in significant degrees of disability for affected individuals. Exercise and medication management are two treatments frequently used to treat Parkinson disease, and although some individuals benefit from these treatments, by what effect exercise works is presently not known. We will examine muscle structure and movement control responses to strengthening exercises and compare them to the therapeutic response observed as a result of medication intake. This process will allow us to better understand the mechanisms underlying the therapeutic effects of strengthening exercise for persons with Parkinson disease.
Idiopathic Parkinson disease (IPD) is the model movement disorder to explore the motor
function of the basal ganglia. (Morris ME, 2005) Alterations in the output of the basal
ganglia lead to reductions in muscle force output and movement amplitude while inactivity
and impaired mobility contribute to the loss of muscle size and strength.
Collectively these factors lead to reductions in the size and speed (hypokinesia) of
functional movements such as gait. Hypokinesia during gait initiation and gait are
biomechanical events that can precipitates movement deficits such as bradykinesia and falls.
Previous studies have suggested that resistance training is beneficial in the management of
persons with PD. Although anatomic, behavioral, and mobility related improvements have been
demonstrated with resistance training intervention, it is unclear if the observed changes
are derived solely from peripheral musculoskeletal changes or from central nervous system
mediated alterations in force output and movement amplitude. The responsiveness of muscle
force, movement amplitude, and hypokinesia to the CNS mediated effects of dopamine
replacement provide a model system to which the effects of resistance training can be
compared. In order to examine this question, we plan to conduct a controlled trial to
rigorously examine the effects of high force resistance training on muscle structure, muscle
force output, and hypokinesia in persons with moderate IPD and in the process, characterize
the potentially differential effects of resistance training effects and dopamine
replacement. This study assembles a team of investigators with experience in high force
resistance training, measurement of the biomechanical and clinical balance function in
persons with PD, and the statistical analysis expertise. Persons with IPD will be recruited,
examined, and if they meet the inclusion criteria will be randomly assigned to one of two
groups (experimental or standard care control). A battery of tests including muscle
structure, muscle force production, and measures of hypokinesia and will be assessed on and
off dopamine replacement medication both prior to and after a 12 week resistance training
intervention. The first specific aim of the study is to determine if high force resistance
training results in improvements in muscle structure, muscle force output, and hypokinesia
in persons with moderate IPD. The second specific aim is to characterize and compare any
differential effects of high force resistance training and dopamine replacement on muscle
force output and hypokinesia in persons with moderate IPD. We hypothesize that dopamine
replacement and resistance training will interact to improve muscle force output and reduce
hypokinesia. In addition, we hypothesize that examination of kinematic patterns during gait
initiation will reveal differential effects on lower extremity hypokinesia. The results of
this study will help to better understand the differential contributions of resistance
training and dopamine replacement on hypokinesia in persons with PD.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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