Constraint Induced Movement Therapy (CIMT)- Neuroimaging Predictors of Positive Response to Constraint (OBI_CIMT)
Hemiplegic Cerebral Palsy
About this trial
This is an interventional treatment trial for Hemiplegic Cerebral Palsy focused on measuring Cerebral Palsy, Hemiplegia, Constraint Induced Movement Therapy
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of Hemiplegic CP secondary to an MCA infarct
- Age between 7 and 16 years
- Ability to co-operate, understand, and follow simple instructions for neuro-imaging outcome measurement: The functional MRI protocol will require some cooperation and the child will need to lie still in a confined place for approximately 45-60 min.
- No previous CIMT within 12-months of study entry or Botulinum toxin upper limb injections within 6-months of study entry.
Exclusion Criteria:
- None
Sites / Locations
- McMaster Children's Hospital, Hamilton Health Sciences
- Thames Valley Children's Centre, London Health Sciences Centre
- Holland Bloorview Kids Rehabilitation Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
CIMT
Comparison
A standardized CIMT protocol will be administered over a three week period. The first week will consist of wearing a below elbow cast on the non-hemiplegic limb followed by a two week CIMT camp (5 hours per day, 5 days per week) where the child/youth wears a constraint splint on the non-hemiplegic hand. The two week camp will follow a standardized CIMT camp protocol ("Hand2Hand" developed at HBKRH) that includes activities that focus on unilateral hemiplegic hand activity in the first week and increasing incorporation of bilateral hand activities in the second week. The camp protocol for CIMT is based on camp protocols utilized successfully in other paediatric research studies.
Standard therapy.