Transcranial Direct Current Stimulation (tDCS)-Enhanced Stroke Recovery
Status: | Completed |
---|---|
Conditions: | Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - 80 |
Updated: | 7/11/2015 |
Start Date: | March 2009 |
End Date: | April 2014 |
Contact: | Timea Hodics, M.D. |
Email: | Timea.Hodics@UTSouthwestern.edu |
Phone: | 214-648-7843 |
TDCS-enhanced Stroke Recovery and Cortical Reorganization
The purpose is to determine whether application of a non-invasive battery powered device
called transcranial direct current stimulation (tDCS) can improve recovery of hand weakness
after stroke beyond what is achievable with rehabilitative treatment alone.
called transcranial direct current stimulation (tDCS) can improve recovery of hand weakness
after stroke beyond what is achievable with rehabilitative treatment alone.
Inclusion Criteria:
- ischemic stroke causing arm weakness within 5-15 days
- no other neurological or psychiatric disease, who are able to perform study tasks
Exclusion Criteria:
- patients younger than 18 or older than 80 years
- patients with more than one disabling stroke
- Patients with bilateral motor impairment
- Patients with poor motivational capacity, history of severe alcohol or drug abuse
- Patients with severe language disturbances, particularly of receptive nature
- Patients with serious cognitive deficits (defined as equivalent to a MMS score of 23
or less)
- Patients with severe uncontrolled medical problems (e.g., seizures, progressive
stroke syndromes, severe rheumatoid arthritis, active joint deformity of arthritic
origin, active cancer or renal disease, end-stage pulmonary or cardiovascular
disease, or a deteriorated condition due to age or others),
- Patients with unstable thyroid disease
- Patients with increased intracranial pressure
- Patients with unstable cardiac arrhythmia
- Patients with contraindication to TMS or tDCS stimulation (pacemaker, an implanted
medication pump, a metal plate in the skull, or metal objects inside the eye or
skull, patients who had a craniotomy, skin lesions at the site of stimulation)
- Patients who are not available for follow-up at 3 and 12 months
- Pregnancy
- Patients with contraindication to MRI will not participate in MRI
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