Stroke Clinical Trial
Official title:
Source of Neurally-Mediated Hand Weakness After Stroke
The purpose of this study is to determine whether neural block and neuromuscular electrical stimulation are effective in treating finger impairment due to stroke.
The incidence of stroke-induced hemiparesis among veterans is likely to rise as this
population ages. Post-stroke hemiparesis is often marked by persistent hand impairment,
which adversely affects both a person's ability to work and his/her quality of life. We
believe that impairment is primarily due to neural, rather than biomechanical, factors. At
the muscle level, these factors relate either to the inability to activate muscles (i.e.,
low muscle activation) or to activate them appropriately (i.e., abnormal muscle
co-activation). Currently it is unclear as to which one is largely responsible for weakness
in the hand as the net mechanical effect, e.g., reduced fingertip force production, could be
the same. Determination of voluntary muscle force generation could help to explain deficits
in fingertip force production in specific directions, as well as to customize treatment
approaches in which force generation ability of some muscles is decreased and others
increased. The goal of this work is to explain the source of neurally-mediated weakness at
the fingertip following hemiparetic stroke, and to design and experimentally test
rehabilitation interventions that attempt to offset this weakness.
As we were refining the protocol to experimentally test a rehabilitation
intervention—involving neural block and stimulation of select muscles to decrease and
increase muscle force generation—it was more challenging than anticipated to locate, using
ultrasound, small nerve branches to individual muscles for selective neural blocking. As a
result we designed additional interventions, using a computer model, that reflected the
physical limitation to implementation which could still hopefully lead to improved fingertip
function. We are seeking novel approaches to locate and block small nerve branches to
individual muscles for an individual muscle-based approach to rehabilitation which we expect
to be an improvement over rehabilitation interventions that target groups of muscles at a
time. The clinical data collected in the study and biomechanical model simulation work
provide guidance for a clinical trial study in the future.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
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