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N/A Completed N=20

Effects of Cardiac Rehabilitation for Individuals With Transient Ischemic Attack

Source: ClinicalTrials.gov NCT00929994 ↗
Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Apr 2019
Primary outcomePrimary: Functional Walk Test — 498.4; 503.2; 564.2 meters — p==0.06

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Functional Walk Test
498.4; 503.2; 564.2 =0.06
PRIMARY
Cardiovascular Fitness (VO2peak)
16.7; 19.1 0.01 sig
SECONDARY
Center for Epidemiologic Studies Depression Scale (CES-D).
6.5; 7.6; 4.3 0.04 sig
SECONDARY
Cognition
26.5; 26.8; 27.1 >0.05

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00929994). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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