Purpose

Strokes often cause a loss of communication ability, referred to as aphasia, as well as cognitive difficulties. Each stroke survivor has a unique pattern of strengths and weaknesses in communication and cognition, and a unique course of recovery. The BUILD study aims to understand the brain basis of these individual differences in stroke outcome. Participants with stroke as well as controls matched in age, educational background, race, and sex are examined using a combination of standardized and in-house tests of language and cognition to provide a detailed profile of strengths and weaknesses. Each participant will have between three and six sessions, including an MRI to measure details of the structure, function, and connections in the brain. The data are analyzed to test how patterns in the stroke lesion explain the patterns of communication and cognitive difficulties, and how patterns in the uninjured parts of the brain explain resilience and recovery from the stroke. Ultimately, we hope that BUILD will guide us toward new targets for brain stimulation treatments or other biologically based treatments that improve language and cognitive abilities after stroke.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

Stroke Survivors: - Age >=18 - Stroke in left hemisphere of brain with or without aphasia, or stroke elsewhere causing aphasia - Learned English at 8 years or younger Controls: - Age >=18 - No history of brain injury resulting from stroke, trauma, infection (i.e. encephalitis), or tumor - Learned English at 8 years or younger

Exclusion Criteria

  • History of other brain conditions that could impact interpretation of results (such as multiple sclerosis, premorbid dementia) - Severe psychiatric condition that would interfere with participation in the study - History of a learning disability that could impact interpretation of results Additional Exclusion Criteria for MRIs: - Pacemaker or magnetic metal in the body that is not MRI compatible - Pregnancy - Claustrophobia

Study Design

Phase
Study Type
Observational
Observational Model
Case-Control
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Stroke Survivors Participants have had a left-hemisphere stroke with or without aphasia, or a stroke elsewhere in the brain causing aphasia. They are given a series of standardized and in-house tests of language and cognition to provide a detailed profile of strengths and weaknesses, plus an MRI.
Controls Participants are matched to aphasia 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 language and cognition to provide a detailed profile of strengths and weaknesses, plus an MRI.

Recruiting Locations

Georgetown University Medical Center
Washington, District of Columbia 20057
Contact:
Sachi Paul, BA
202-687-5205
sp1446@georgetown.edu

More Details

Status
Recruiting
Sponsor
Georgetown University

Study Contact

Alycia Laks, MS, CCC-SLP
202-687-5205
al1579@georgetown.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.