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

Primary Purpose

Stroke, Broca's Aphasia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Cortical Electrical Stimulation
Sponsored by
Northstar Neuroscience
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Cortical Electrical Stimulation, Ischemic Stroke, Broca's Aphasia, Speech Rehabilitation, Functional MRI

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Rehabilitation Institute of Chicago
  • Univ. of Chicago

Outcomes

Primary Outcome Measures

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 Outcome Measures

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

Full Information

First Posted
September 12, 2005
Last Updated
September 19, 2007
Sponsor
Northstar Neuroscience
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1. Study Identification

Unique Protocol Identification Number
NCT00170703
Brief Title
Assessment of Cortical Stimulation Combined With Rehabilitation to Enhance Recovery in Broca's Aphasia.
Official Title
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.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2007
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Northstar Neuroscience

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Broca's Aphasia
Keywords
Cortical Electrical Stimulation, Ischemic Stroke, Broca's Aphasia, Speech Rehabilitation, Functional MRI

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
8 (false)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Cortical Electrical Stimulation
Primary Outcome Measure Information:
Title
Aphasia Quotient on the Western Aphasia Battery (WAB-AQ) at follow-up week 1
Title
Measures of speech rate obtained from Language Sample Analysis at follow-up week 1
Secondary Outcome Measure Information:
Title
Serious Adverse Event rate at follow-up weeks 1, 6 & 12-week
Title
Aphasia Quotient on the Western Aphasia Battery (WAB-AQ) at follow-up weeks 6 & 12
Title
Measures of speech rate obtained from Language Sample Analysis at follow-up weeks 6 & 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Facility Information:
Facility Name
Rehabilitation Institute of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Univ. of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26704258
Citation
Cherney LR. Epidural Cortical Stimulation as Adjunctive Treatment for Nonfluent Aphasia: Phase 1 Clinical Trial Follow-up Findings. Neurorehabil Neural Repair. 2016 Feb;30(2):131-42. doi: 10.1177/1545968315622574. Epub 2015 Dec 23.
Results Reference
derived

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

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