Hemiplegic Cerebral Palsy Clinical Trial
Official title:
Childhood Hemiplegic CP Integrated Neuroscience Discovery Network (CP-NET) Theme IIIa: Constraint Induced Movement Therapy (CIMT)- Neuroimaging Predictors of Positive Response to Constraint
CIMT has shown great promise in helping children and adults regain lost function in a disabled limb by forcing its use through an intensive motor training program and constraining the unaffected arm with a cast. However, relatively little is known about the underlying mechanisms of CIMT in hemiplegic CP. This project will use an integrated translation model to explore neuroimaging predictors of a positive clinical response to CIMT.
The primary research objective is to evaluate neuroimaging predictors of a positive response
to CIMT in children with hemiplegic CP secondary to a middle cerebral artery territory
stroke (MCA). A focus on the MCA territory is chosen as (1) it targets children with
significant hand impairment who have the potential to benefit from CIMT, (2) is the most
common neuropathological subtype, and (3) allows for enhanced homogeneity for the matching
of case and comparison groups. The primary research question is: In children aged 7 to 16
years with hemiplegic CP secondary to an MCA stroke, are there neuroimaging predictors of a
positive response to CIMT, a positive response being defined by an improvement in the
Assisting Hands Assessment (AHA) one month after CIMT?
Neuroimaging predictor variables include laterality index (LI) of the primary M1 and S1
areas on fMRI, IHI evaluated by resting state fMRI, dissociation of the M1 and S1 for the
hemiplegic hand measured by fMRI, size and vascular distribution of the MCA lesion with T2
weighted MRI, and white matter tract abnormality with Diffusion Tensor Imaging (DTI). We
hypothesize that a negative LI, a non-dissociated M1 and S1, low IHI, small size of
infarction, and large size of the contralateral corticospinal tract will predict a positive
response to constraint. An evaluation of the neuroimaging predictor variables on the
persistence of a positive response to CIMT at 6 months as measured by the AHA will also be
explored. A secondary objective will evaluate change in the neuroimaging variables from
baseline to one month post CIMT by comparing children in the case group who have received
CIMT and a comparison group who are matched on baseline QUEST scores.
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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