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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UNKNOWN
NA
300 participants
INTERVENTIONAL
2013-07-31
2025-01-31
Brief Summary
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This study will also collect fitness, walking, balance, and brain health outcome measures at baseline and post all other MERCE exercise and robotics interventions.
Detailed Description
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Individuals with cerebrovascular risk factors (e.g., hypertension, diabetes), minor stroke (nondisabling stroke in terms of community or home walking capability), TIA (warning stroke), or silent stroke (seen by brain imaging, but no paralysis or obvious stroke signs or symptoms) will be entered into a 6 month duration exercise class.
Initial medical and neurological evaluation will be conducted by a credentialed Clinician to assure that individuals are eligible and that they are medically and neurologically approved for participation in a low intensity aerobic exercise class. All subjects will have approval of their primary care provider, documenting their awareness and medical approval for their patient to enter into a low to moderate exercise intensity class. This is the same medical clearance that is already Institutional Review Board approved and is in use for the similar exercise class for stroke and neurologic disability in Howard County Department of Aging Senior Centers. Before starting the exercise, all subjects will be given a series of baseline testing: 1) walking and balance tests to characterize their mobility performance capacity (timed walks, Short Physical Performance Battery, Functional Reach, Berg Balance Test, modified dynamic gait index, and 4 square stepping, 2) a 12 hour battery of written and computer based cognitive function and mood tests and questionnaires, and 3) MRI that lasts about 1 hour that includes pictures of the brain . All of these tests will be repeated at midpoints (i.e., 3 months) and at the end of the training program (6 months, MRIs are performed only at baseline and 6 months). The exercise class will consist of supervised walking as well as bar and chair exercises to address upper and lower extremity function. The class will occur 3 times per week for 6 months.
Individuals are instructed to perform select parallel exercises at home the remaining days of the weeks and record activities in a homework logbook.
This protocol is being designed in a modular fashion to collect the same outcomes at baseline and post all other MERCE exercise and robotics interventions.
Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Group Exercise Class
6 month group balance/exercise class, three days a week - up to one hour. Exercise program includes walking around a track, bodyweight/balance exercises, and an obstacle course.
Exercise
6 month group exercise class
Testing
Subjects enrolled in other MERCE exercise and robotics interventions will receive balance/walking tests, MRI with famous name recognition task, and cognitive testing pre and post their intervention.
No interventions assigned to this group
Interventions
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Exercise
6 month group exercise class
Eligibility Criteria
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Inclusion Criteria
* Able to rise from a chair unaided
* Completion of all regular post-stroke physical therapy (if applicable)
* Able to walk 30 feet without human assistance
Exclusion Criteria
* unstable angina
* recent (\< 3 months) myocardial infarction or congestive heart failure (NYHA category II)
* hemodynamically significant valvular dysfunction
* peripheral arterial obstructive disorder with claudication
* major orthopedic, chronic pain, or non-stroke neuromuscular disorders restricting exercise
* pulmonary or renal failure
* poorly controlled hypertension (\>190/110), measured on at least two separate occasions
* recent hospitalization for severe disease or surgery
* severe or global receptive aphasia which confounds reliable testing and training
* Other medical condition precluding patient participation in this study as per medical judgment of study team
* Untreated major depression
* Pregnancy
* Alcohol consumption \> 3 oz. liquor, or 3 x 4 oz glasses of wine, or 3 x 12 oz. beers per day, by self-report
* Dementia and other major cognitive deficits (based upon clinical evaluation)
18 Years
95 Years
ALL
Yes
Sponsors
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University of Maryland
OTHER
Baltimore VA Medical Center
FED
Responsible Party
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Rich Macko
Associate Director of Research for the GRECC
Principal Investigators
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Emily Byrne, BS
Role: STUDY_DIRECTOR
Baltimore VA Medical Center
Locations
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Baltimore VA Medical Center
Baltimore, Maryland, United States
Countries
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Central Contacts
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Facility Contacts
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Emily Byrne, BS
Role: primary
Other Identifiers
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BaltimoreVAMC
Identifier Type: -
Identifier Source: org_study_id