Cerebral Palsy Clinical Trial
Official title:
Early Childhood Constraint Therapy for Sensory/Motor Impairment in Cerebral Palsy
This is a prospective interventional study involving young children who will all receive non-invasive, passive assessments of sensory and motor function. In addition a subpopulation of young children with cerebral palsy will participate in a randomized controlled trial of constraint-induced movement therapy, a routinely prescribed therapy used in clinical practice for children with motor difficulties. The study attempts to apply a rigorous scientific approach to study a widely used but poorly studied practice. The design is an RCT with wait-list controls to allow all children to benefit from the therapy, even if they are randomized to the control group. All children, regardless of group allocation will continue with their standard of care occupational and physical therapy throughout the study.
Cerebral palsy (CP) is the most common physical disability in childhood.1 It affects 3.6/100
children in the US2 with ~10,000 new diagnoses every year. The prevalence of CP in developing
countries is estimated to be ~5-10 times greater. CP is a disorder resulting from sensory and
motor impairments due to perinatal brain injury, with lifetime consequences that range from
poor adaptive and social function to communication and emotional disturbances,9 all
contributing to a shortened life expectancy. The societal costs are difficult to estimate but
the financial burden is well over $1 M per life affected. A growing number of evidence-based
therapies aim to improve gross motor function through changes in body structures and function
in children with CP (e.g. hip surveillance, surgery). However, infants with CP have a
fundamental disadvantage in recovering motor function: they do not receive accurate sensory
feedback from their movements, leading to neglect of an affected extremity and difficulty
learning new movements, a process called developmental disregard (DD). As a consequence, even
children who receive time- and resource-intensive standard therapies have stable or declining
motor function and developmental trajectories that do not "catch up" to those of typically
developing children. DD can then lead to school-age learning problems, decreased
participation in physical and social activities and costly long-term mental and physical
morbidities.
Constraint-Induced Movement Therapy (CIMT) is one of the few effective neurorehabilitative
strategies shown to improve upper extremity motor function in adults and older children with
CP, potentially overcoming developmental disregard. It is mainly applicable to CP patients
who are diagnosed with asymmetric or hemiparetic forms of the disorder, in which one side of
the body is more affected than the other. CIMT is based on the premise that preferential use
of an affected upper extremity (by constraining the less affected one), and shaping with
repetition of movement by skilled therapists, can overcome neglect and restore function of
that extremity.
The investigators are conducting a randomized trial of CIMT in children with CP using a
wait-list control group. This design allows every child with CP to eventually receive the
treatment and avoids issues of equipoise. The RCT portion of the study extends only for a
7-month period, from baseline to 6 months after the 1-month CIMT ends. For CP wait-listed
controls, the study continues for 6 months following the CMIT intervention, separate from the
completed RCT. We will reference data from both groups to a cohort of typically developing
(TD) children to determine developmental trajectories.
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