Comprehensive Cardiac Rehabilitation Feasibility After Stroke
- Conditions
- Stroke, Ischemic
- Interventions
- Behavioral: Exercise
- Registration Number
- NCT03944668
- Lead Sponsor
- HealthPartners Institute
- Brief Summary
Comprehensive Cardiovascular Rehabilitation Feasibility After Stroke (CCR FAST) will evaluate the feasibility of enrolling Regions Hospital stroke patients in a Comprehensive Cardiovascular Rehabilitation (CCR) program. CCR will include aerobic exercise and patient education (regarding risk factors and medication compliance), similar to the rehabilitation program for cardiac disease patients. The overall goal of CCR FAST is to demonstrate the feasibility and safety of including stroke patients in a CCR program, while examining the clinical value in reducing stroke recurrence, myocardial infarction, readmission, and mortality in stroke patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 17
- Age ≥ 18 years
- Patient has suffered an ischemic stroke
- Patient should be ambulatory (non-disabling stroke) to be able to participate in the CCR exercise program
- Patient is able to start cardiac rehabilitation within 2 weeks of stroke
- No baseline (index admission for ischemic stroke) MRI completed
- Life expectancy < 1-year
- Presence of brain hemorrhage: intracerebral hemorrhage, subarachnoid hemorrhage, subdural hematoma, or epidural hematoma
- Concurrent diagnosis of seizure disorder
- Patient with moderate or severe neurologic deficits, limiting their ability to participate in the CCR exercise program
- Cardiopulmonary conditions preventing the patient from participation, such as severe heart failure, severe aortic stenosis, and exercise-induced asthma
- Patient with cognitive dysfunction impairing their ability to follow directions
- Anticipated procedures such as carotid stenting, carotid endarterectomy, and intracranial aneurysm coiling
- Patient unable to commit to the frequent visits of the CCR program
- Participation in other interventional research (observational research is allowed)
- Unable to have brain MRI
- Non-English speaker
- Pregnant women
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Intervention Exercise Exercise intervention
- Primary Outcome Measures
Name Time Method Attendance Rate 12 weeks 75% attendance at comprehensive cardiovascular rehabilitation (CCR) sessions
- Secondary Outcome Measures
Name Time Method Hospital Readmission 6 month rate, for a cardiovascular or cerebrovascular indication
Number of Participants With or Without Silent Stroke 6 month rate, on MRI
Number of Patients With or Without Recurrent Stroke 6 month Recurrent stroke in follow-up period
Number of Participants With or Without Myocardial Infarction 6 month Myocardial infarction in follow-up time
Number of Participants Without Death 6 month rate
Trial Locations
- Locations (3)
Regions Hospital
🇺🇸Saint Paul, Minnesota, United States
Regions Hospital Outpatient Cardiopulmonary Rehabilitation Clinic
🇺🇸Saint Paul, Minnesota, United States
HealthPartners Neuroscience Center
🇺🇸Saint Paul, Minnesota, United States