Acupuncture as Complementary Therapy for Cerebral Palsy
Cerebral Palsy
About this trial
This is an interventional treatment trial for Cerebral Palsy focused on measuring cerebral palsy; acupuncture
Eligibility Criteria
Inclusion Criteria: Children between the ages of 12 and 72 months. Children with a diagnosis of spastic cerebral palsy (CP) or mixed type CP where spasticity is the dominant feature. Exclusion Criteria: Age - Any child with CP who is younger than 12 months or older than 72 months. Etiology - Any damage to the CNS that either (a) is not static in nature, such as degenerative or progressive central nervous disorders, or (b) occurred after the first year of life, or (c) any child who has a phenotypic pattern suggesting a chromosomal abnormality (e.g., trisomy 13 or 18). Diagnosis - Children for whom the diagnosis of spastic CP or mixed-type CP with spasticity as the dominant feature cannot be established with absolute certainty, or children with dyskinetic CP. Rationale - To assure subject homogeneity, in cases in which there is disagreement between the physicians with respect to the diagnosis of a child, even if one of the physicians feels certain that a child has spastic CP, the children would be automatically excluded. Co-morbidities - Medical conditions, whether acute or chronic, for which acupuncture or intense 'conventional' therapies are considered contraindicated. Rationale - assuring participants' safety. Co-interventions - Any child receiving or scheduled to receive treatment(s) during the study period that may confound the results (e.g., an orthopedic or neurosurgical procedure, Botulinum toxin injections, a Baclofen pump or hyperbaric oxygen treatment). Rationale -To avoid a threat to causal inferences. Parallel participation in another CP clinical trial. Rationale - To avoid pragmatic and ethical issues that may arise as a result of a conflict of interests and limited resources.
Sites / Locations
- The University of Arizona, Department of Pediatrics
- Beijing Children's Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Group 1
Group 2
Intensely administered (5 times per week for 12wk) physical therapy, occupational therapy, and hydrotherapy with acupuncture
Intensely administered (5 times per week for 12wk) physical therapy, occupational therapy, and hydrotherapy without acupuncture