Stroke Clinical Trial
Official title:
TMS as a Biological Marker of Neuroplasticity
NCT number | NCT02867670 |
Other study ID # | 818784 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | July 2013 |
Est. completion date | June 2020 |
Verified date | July 2020 |
Source | University of Pennsylvania |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
TMS is a non-invasive brain stimulation technique, which can be used to change the activity of a person's brain cells without needles or surgery. In this study, the invesigators are interested in the brain's ability to adapt (also called "neuroplasticity") and regain language functioning after a stroke—specifically, they want to determine whether how a person's brain responds to TMS in the short term can be used to predict how well they will recover language abilities in the long term.
Status | Completed |
Enrollment | 41 |
Est. completion date | June 2020 |
Est. primary completion date | June 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Must have Aphasia due to stroke - Stroke must have occurred at least 6 months ago - Native English speaker - Willing & able to have a MRI Exclusion Criteria: - Disorders of the brain other than stroke (i.e. tumor, Parkinsons, cancer... etc.) - History of seizures/ or epilepsy - Pacemaker or other implanted electronic devices - Consumption of medications that lower seizure threshold - History of psychiatric disorders - History of tinnitus - Current abuse of drugs or alcohol - Pregnant or plan to get pregnant |
Country | Name | City | State |
---|---|---|---|
United States | University of Pennsylvania | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pennsylvania |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Transient TBS-induced changes in motor evoked potentials (MEPs) | Single-Pulse TMS will be used to measure MEPs prior to and after stimulation. When measuring MEPs, single pulses of TMS will be administered at approximately 120% of motor threshold, and with a minimum interstimulus interval of 5 seconds. Mean MEP amplitudes will be calculated by averaging the MEP amplitudes generated by 20 pulses. MEP measures will be obtained three times in order to establish a stable baseline. This procedure will be followed by TBS delivered to the optimal site in the motor cortex. TBS will be applied to the region of the primary motor cortex (M1) representing the hand. After TBS, MEPs will be acquired, at 0-, 10-, 20-, 30-, 40-, and 60-min post-stimulation. | Up to 2 week | |
Primary | Transient TBS-induced changes in language performance | Participants will be asked to perform a 40-item picture naming task pre/post TBS stimulation. Stimulation will occur at language cortex and vertex (order will be counterbalanced). Transient changes in naming abilities will be measured directly by assessing naming performance. | Up to 4 weeks | |
Secondary | Safety and Tolerability of TBS in patient with aphasia | We will collect the number of patients with TMS-related adverse events. | Through study completion |
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