Effects of Cardiac Rehabilitation for Individuals With Transient Ischemic Attack
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|ClinicalTrials.gov Identifier: NCT00929994|
Recruitment Status : Completed
First Posted : June 30, 2009
Last Update Posted : November 13, 2015
It is hypothesized that the addition of formal cardiac rehabilitation to standard care will result in long-term improvements in cardiovascular fitness and functional capacity in individuals who have suffered a transient ischemic attack (TIA) or minor stroke.
Furthermore, it is proposed that the addition of cardiac rehabilitation will influence stroke risk, physical activity participation, strength, and quality of life.
|Condition or disease||Intervention/treatment|
|Transient Ischemic Attack||Behavioral: Cardiac Rehabilitation|
|Study Type :||Observational|
|Actual Enrollment :||21 participants|
|Official Title:||Effects of Cardiac Rehabilitation for Individuals With Transient Ischemic Attack|
|Study Start Date :||March 2010|
|Primary Completion Date :||November 2014|
|Study Completion Date :||November 2014|
Participants in this group will participate in Cardiac Rehabilitation, carrying out an exercise program which will last 6 months and combine both resistance and aerobic training.
Behavioral: Cardiac Rehabilitation
Individualized cardiac rehabilitation for 6 months, including health education sessions, as well as supervised exercise classes which include aerobic and resistance training.
- Primary outcomes include improvements in cardiovascular fitness, functional capacity, and physical activity levels in individuals with TIA. This will be measured using a cardiopulmonary exercise test and a 6 minute walk test. [ Time Frame: Baseline, 6 months, 12 months ]
- Secondary outcome measures are plasma lipid analysis, questionnaires pertaining to quality of life, physical activity and diet diaries, and results from the Montreal Cognitive Assessment and MRI analysis. [ Time Frame: Baseline, 6 months, 12 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00929994
|Toronto Rehabilitation Institute - Rumsey Center|
|Toronto, Ontario, Canada, M4G 1R7|
|Principal Investigator:||Dina Brooks, PhD||Toronto Rehabilitation Institute|
|Principal Investigator:||William E McIllroy, PhD||University of Waterloo|
|Principal Investigator:||Paul Oh, MD||Toronto Rehabilitation Institute|
|Principal Investigator:||Sandra Black, MD||Sunnybrook and Women's College Health Centre|