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Clinical Trials/NCT00929994
NCT00929994
Completed
Not Applicable

Effects of Cardiac Rehabilitation for Individuals With Transient Ischemic Attack

Toronto Rehabilitation Institute1 site in 1 country20 target enrollmentMarch 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Transient Ischemic Attack
Sponsor
Toronto Rehabilitation Institute
Enrollment
20
Locations
1
Primary Endpoint
Functional Walk Test
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

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 depressive symptoms and cognition.

Detailed Description

A transient ischemic attack (TIA) is defined as an episode of neurological dysfunction caused by focal brain ischemia lasting less than 24 hours. Once an individual has suffered a TIA, preventative measures can be taken to target modifiable risk factors, one of which is physical inactivity. The current proposal focuses on the use of an established model of care (cardiac rehabilitation (CR)) and applies it to those who have suffered a TIA in order to maximize physical activity and minimize risk of future cardiovascular events. This will be a one-group pre/post design study with a 3 month non-intervention period. Participants will undergo measures at baseline and 3 months (non intervention period) then after 6 months of cardiac rehabilitation (cardiovascular fitness, 6 minute walk test, cognition, and depressive symptoms).

Registry
clinicaltrials.gov
Start Date
March 2010
End Date
November 2014
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dina Brooks

Professor

Toronto Rehabilitation Institute

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with TIA
  • Three months post-TIA
  • Ability to understand the process and instructions for exercise training and provide informed consent

Exclusion Criteria

  • Resting Blood Pressure greater than 160/100 despite medication
  • Other cardiovascular morbidity which would limit exercise tolerance (heart failure, abnormal BP responses or STsegment depression \> 2 mm, symptomatic aortic stenosis, complex arrhythmias)
  • Current and extensive exercise participation
  • Hypertrophic Cardiomyopathy
  • Unstable Angina
  • Orthostatic BP decrease of \> 20 mm Hg with symptoms
  • Other musculoskeletal impairments which would limit the participants ability to walk sufficient durations
  • Pain or other co-morbidities (e.g., unclipped aneurysms, uncontrolled seizures etc.) which would preclude participation
  • Cognitive or behavioural issues that would limit participation in exercise testing and training

Outcomes

Primary Outcomes

Functional Walk Test

Time Frame: Baseline, 3 months, 6 months (Six Minute Walk Distance)

6 minute walk test: the longest distance a person can walk for a duration of 6 minutes

Cardiovascular Fitness (VO2peak)

Time Frame: Baseline (after the 3 month non-intervention period) and after 6 months of participation.

To measure cardiovascular fitness, a stress test on either an upright cycle ergometer (Ergoselect 200P, Germany), or a treadmill (same modality pre- and post-training) was performed depending on patient balance and comfort.

Secondary Outcomes

  • Cognition(Baseline and 3 months (non-intervention period), after 6 months of cardiac rehabilitation participation)
  • Center for Epidemiologic Studies Depression Scale (CES-D).(Baseline and 3 months (non-intervention period), after 6 months of cardiac rehabilitation participation)

Study Sites (1)

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