Doctors use different treatments for people with Cerebral Palsy. Surgery is one option. Botulinum toxin injections are another option; these are given directly into spastic muscles to weaken them temporarily. Regular ongoing treatment (splinting, stretching and exercises) is another option. The investigators want to find out if surgery works better than Botulinum Toxin (Botox) injections or regular ongoing treatment (therapy), and if the effects of Botulinum Toxin injections last for longer than six months.
The specific aims of this study and the methodology for achieving them are: 1. To determine if tendon surgery for the forearm, wrist and thumb deformities of UECP is more effective than Botulinum toxin injections or regular ongoing treatment at improving function and quality of life for children with UECP. Children who are candidates for tendon surgery will be prospectively randomized to one of three treatment groups: standard tendon surgery, a series of three Botulinum toxin injections over a period of 12 months, and regular ongoing treatment. Validated tests of cognition, function and quality of life with tests of stereognosis and range of motion will be administered before, during and after treatment in order to compare outcomes of the three treatment groups. 2. To determine if serial Botulinum toxin injections have long-term beneficial effects on upper extremity function which outlast their paralytic effects. Botulinum toxin has been shown to have beneficial effects on UE function while the muscles injected remain weakened by the toxin. Clinicians have theorized that improvements in UE function are maintained after the toxin wears off, but this has not been proven. Children randomized to the Botulinum toxin injection group will receive 3 injections. Their function will be tested before the first injection, while the paralytic results of the second injection are still in effect, and after the paralytic effects of the third injection have worn off, and the results compared in order to determine if functional improvements outlast the medicinal effects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Enrollment
Shriners Hospitals for Children Northern California
Sacramento, California, United States
Alfred I duPont Childrens Hospital
Wilmington, Delaware, United States
Children's National Medical Center
Washington D.C., District of Columbia, United States
Shriners Hospitals Upper Extremity Evaluation (SHUEE)
Time frame: Initial, 6 mon, 1 year
Box & Blocks
Time frame: Initial, 6 mon, 1 year
Assisting Hand Assessment (AHA)
Time frame: Initial, 6 mon, 1 year
Scores on questionnaires that assess participation and patient satisfaction at initial, 6 month and 1 year post intervention.
Time frame: Initial, 6 mon, 1 year
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