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Assessment of Cortical Stimulation Combined With Rehabilitation to Enhance Recovery in Broca's Aphasia.

Assessment of the Safety and Effectiveness of Targeted Sub-Threshold Epidural Cortical Stimulation Delivered Concurrent With Speech-Language Rehabilitation to Enhance Recovery in Patients Suffering From Broca's Aphasia, Following a Stroke.

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00170703
Enrollment
8
Registered
2005-09-15
Start date
2004-12-31
Completion date
2007-09-30
Last updated
2007-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Broca's Aphasia, Stroke

Keywords

Cortical Electrical Stimulation, Ischemic Stroke, Broca's Aphasia, Speech Rehabilitation, Functional MRI

Brief summary

The primary objective of this feasibility study is to evaluate the safety and effectiveness of targeted sub-threshold epidural cortical stimulation delivered concurrent with speech-language rehabilitation activities to enhance recovery in study subjects suffering from Broca's aphasia (the inability to speak or to organize the muscular movements for speech), following a stroke.

Detailed description

Stroke is the third leading cause of death and the most common cause of disability in the United States. According to the American Stroke Association, the prevalence of stroke in the U.S. is approximately 4.8 million with approximately 700,000 additional strokes occurring annually. Approximately 150,000 to 250,000 stroke survivors becoming severely and permanently disabled each year. A common neurological deficit among these stroke survivors, and thus a substantial contributor to post-stroke disability is Broca's aphasia, a condition in which the patient is unable to speak normally, as they cannot effectively organize the muscular movements required for speech. Broca's aphasia is often referred to as non-fluent or motor aphasia as essentially the patient has impaired motor abilities for speech and thus, become non-fluent in speech/language. The loss of speech for these patients is extremely debilitating and has enormous social and economic impact to the quality of life for these patients. Presently, the only treatment available for patients with Broca's aphasia is speech-language rehabilitation. However, with rehabilitation only, many patients achieve a less than satisfactory improvement in speech-language function and thus, are left with significant disability. Since Broca's aphasia is largely due to an impairment of language-related motor function, researchers and clinicians believe it is very likely that cortical stimulation in conjunction with speech rehabilitation may also enhance recovery of language motor function for Broca's aphasia patients. This study proposes to evaluate the safety and effectiveness of such cortical electrical stimulation in study subjects with Broca's aphasia after stroke, delivered concurrent with speech-language rehabilitation. In addition to evaluating changes from baseline level, safety and efficacy measures will be compared to patients who undergo the same speech-language rehabilitation activities but without cortical stimulation. The two study groups will be compared to determine the degree to which the aphasia can be improved beyond rehabilitation alone by epidural stimulation of a targeted cortical region.

Interventions

DEVICECortical Electrical Stimulation

Sponsors

Northstar Neuroscience
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subjects must have an ischemic stroke. * Subjects must have a language dominant left hemisphere. * Subjects must be diagnosed as having predominantly Broca's aphasia. * Age 21 years or older.

Exclusion criteria

* Primary hemorrhagic stroke. * Any additional stroke associated with incomplete speech recovery. * Any neurologic or physical condition that impairs speech function. * History of seizure disorder. * Global aphasia or inability to participate in routine speech therapy. * Untreated or inadequately treated depression. * History of traumatic brain injury, or spontaneous subdural or epidural hematoma that has resulted in a fixed (stable) speech-language deficit. * Major active psychiatric illness that may interfere with required study procedures. * Contraindication to magnetic resonance (MR) imaging.

Design outcomes

Primary

MeasureTime frame
Aphasia Quotient on the Western Aphasia Battery (WAB-AQ) at follow-up week 1
Measures of speech rate obtained from Language Sample Analysis at follow-up week 1

Secondary

MeasureTime frame
Serious Adverse Event rate at follow-up weeks 1, 6 & 12-week
Aphasia Quotient on the Western Aphasia Battery (WAB-AQ) at follow-up weeks 6 & 12
Measures of speech rate obtained from Language Sample Analysis at follow-up weeks 6 & 12

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026