Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2023-01-12
2028-08-31
Brief Summary
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Participants will complete a battery of tests of reading, speech, language, and thinking abilities. In addition, some participants will complete an MRI. Sessions will be completed across approximately 2-6 weeks, but may be extended depending on participants' schedules and availability. Some participants will be invited to repeat these procedures once or twice in approximately 3-12 months to monitor for changes in reading abilities and MRI measurements over time.
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Stroke Survivors
Participants have had a left-hemisphere stroke, or a stroke elsewhere in the brain causing aphasia or alexia (i.e., reading difficulties). They are given a series of standardized and in-house tests of reading, language and cognition to provide a detailed profile of strengths and weaknesses, plus an MRI.
No interventions assigned to this group
Controls
Participants are matched to the stroke cohort in age, educational background, race, and gender but have no history of brain injury. They are also given a series of standardized and in-house tests of reading, language and cognition to provide a detailed profile of strengths and weaknesses, plus an MRI.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Age \>= 18
* Learned English at 8 years or younger
* Brain injury resulting from stroke
Controls:
* Age \>= 18
* Learned English at 8 years or younger
Exclusion Criteria
* Severe psychiatric condition that would interfere with participation in the study
* History of diagnosed learning disorder
* Hearing or vision loss that interferes with performance on behavioral tests even after correction with glasses/hearing aids.
* Inability to follow study procedures despite maximal support
* Presence of metal in the body that is incompatible with MRI
* Pregnancy
* Claustrophobia
18 Years
ALL
Yes
Sponsors
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MedStar National Rehabilitation Network
OTHER
National Institute on Deafness and Other Communication Disorders (NIDCD)
NIH
Georgetown University
OTHER
Responsible Party
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Principal Investigators
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Peter Turkeltaub, MD,PhD
Role: PRINCIPAL_INVESTIGATOR
Georgetown University; MedStar National Rehabilitation Hospital
Locations
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Georgetown University Medical Center
Washington D.C., District of Columbia, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ReadMap
Identifier Type: -
Identifier Source: org_study_id
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