The Effect of Aerobic Exercise on Learning After Stroke
Phase 1
Completed
- Conditions
- Stroke
- Interventions
- Behavioral: Rehabilitation exercise
- Registration Number
- NCT00228306
- Lead Sponsor
- University of Kansas
- Brief Summary
Determine if attaining aerobic fitness is beneficial in producing cortical neuroplasticity in individuals with chronic stroke.
- Detailed Description
Crossover clinical trial. Experimental group undergoes 3x/wk/6 months of aerobic conditioning. Control group performs usual daily activities. All participants will be assessed with cognitive and motor behavioral testing at baseline, 3, 6, 9 and 12 months.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 38
Inclusion Criteria
- Single ischemic stroke occuring 6-72 months prior
- Fugl-Meyer score (upper + lower extremity) 45 or greater
- Mini mental status score of >23
- approval of the subject's medical doctor
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Exclusion Criteria
- already performing >20 min of cardiovascular exercise 3x/wk or more
- alcohol consumption of >2 oz. liquor, 8 oz. wine or 24 oz beer/day
- cardiac history of unstable angina, recent myocardia infarction within the last 3 months, congestive heart failure, significant valve dysfunction
- medical history of recent hospitalization (> 3 months) for medical illness
- symptomatic peripheral arterial occlusive disease
- orthopedic or chronic pain conditions restricting exercise
- pulmonary or renal failure
- active cancer
- unstable hypertension (>160/100 mmHg)
- diabetes mellitus (fasting glucose > 180 NG./dk, HgA1C > 10%) that is unable to be controlled < month
- receptive or expressive aphasia as indicated on MMSE
- multiple strokes or other neuromuscular conditions
- major depression that is untreated using the Beck depression inventory
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description 1 Rehabilitation exercise -
- Primary Outcome Measures
Name Time Method Motor learning behavioral measures; executive function behavioral measures. Baseline, 8 weeks, 12 weeks
- Secondary Outcome Measures
Name Time Method Peak V02 and other aerobic capacity measures. Physical disability measures. Baseline, 8 weeks, 12 weeks
Trial Locations
- Locations (1)
University of Kansas Medical Center
🇺🇸Kansas City, Kansas, United States