- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01592357
The Effects of Tai Chi in Older Patients With Cardiovascular Disease
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The role of exercise training is well established for cardiac patients to improve fitness and clinical outcomes. Many older cardiac patients even if they initially participate do not maintain regular exercise for a number of reasons. As the population ages there is a need to evaluate other forms of exercise training that may be used alone or in conjunction with standard approaches. Tai Chi is a potentially beneficial exercise for older cardiac patients because it is low-intensity exercise especially suited for unfit and elderly patients. There has been little rigorous evaluation, especially in the cardiac populations, of Tai Chi.
The main objective of this study is to assess the effects of Tai Chi compared to "sham exercise" in cardiac patients that have completed a program of cardiac rehabilitation. The investigators hope to show that six months of Tai Chi training compared to "sham exercise" (with all participants instructed to maintain their standard exercise program), will improve gait speed, exercise capacity, health related quality of life, cognitive function and balance.
This is a single blind randomized controlled trial of 200 cardiac patients, great than or equal to 60 years of age, who have completed six months of cardiac rehabilitation at the Hamilton Health Science Cardiac Health and Rehabilitation Centre. Participants will be randomized to receive either the short and simple 8-forms Tai Chi routine or "sham exercise". The participants in the study will train for a period of six months.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ontario
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Hamilton, Ontario, Canada, L8L 2X2
- Cardiac Health & Rehabilitation Centre, Hamilton Health Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Walking Speed < or = 1.3 m/sec during the gait speed assessment.
- Evidence of cardiovascular disease based on a diagnosis of previous myocardial infarction, angiographic findings of coronary artery disease, previous percutaneous coronary intervention, or previous coronary artery bypass graft surgery.
- Local resident, with available transportation to the Cardiac Health and Rehabilitation Centre (CHRC) at the Hamilton Health Sciences General Division.
- Ability to understand written and verbal instructions and provide written informed consent.
- Stable cardiac medical therapy as demonstrated by no change in medication during the 3 months prior to randomization.
- Previous completion of the 6 month Cardiac Rehabilitation program (including exercise training component) at the CHRC.
Exclusion Criteria:
- New York Heart Association Functional class IV symptoms of shortness of breath or angina.
- Development of angina or ST segment depression of > 1 mm during symptom limited exercise testing at < 80% of predicted maximum power output.
- Development of dysrhythmias during exercise (> Lown grade 2).
- Resting blood pressure greater than 160 mmHg systolic or 90 mmHg diastolic.
- Abnormal blood pressure response to clinical exercise testing (decrease in systolic pressure below resting; decrease of > 20 mmHg in systolic pressure after the normal exercise increase; rise in diastolic blood pressure of > 15 mmHg; maximal systolic blood pressure in excess of 250 mmHg).
- Maximum heart rate < 100 beats per minute in the absence of beta blocker therapy.
- Respiratory limitation as assessed by pre-exercise pulmonary function testing (documented restrictive or obstructive lung disease; based on forced expired volume in 1 sec and/or vital capacity measurements < 70% of predicted).
- Major orthopedic disability.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Tai Chi
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A short and simple 8-forms Tai Chi routine will be used in this study.
This routine has been previously standardized and field tested.
Participants will be coached, by a certified Tai Chi instructor, in practicing the proper mechanics of executing each of the eight physical movements comprising the 8-forms of Tai Chi.
A brief 5 minute period of walking calisthenics pertinent to Tai Chi movements, postures and diaphragmatic breathing will take place before training to warm up and after training to cool down.
The Tai Chi training will be 2 times a week and the total exercise time, including warm-up and cool down, will be 50 minutes for each session.
Over a period of 12 weeks, the participants will learn all 8-forms and continue practicing them for the final 12 weeks of the training period.
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Sham Comparator: Sham Exercise
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The sham exercise (control) group will be involved in low-intensity stretching exercises two times per week.
These exercises will be designed as a "sham exercise" condition.
A brief 5 minute period of walking will take place before the sham exercise to warm up and after the sham exercise to cool down.
Sham exercise sessions will include stretching exercises of the neck, trunk and extremities.
The total exercise time for the "sham exercise" group will be 50 minutes and participants will meet 2 times per week for a period of 24 weeks.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Gait speed following 6 months of Tai Chi or sham exercise training
Time Frame: 24 weeks
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Gait speed will be measured by having participants walk a 4 metre course at their usual speed.
There will be a 1-metre start-up before starting the timing for the walk over 4 metres.
Each participant will be timed for 2 walks and the faster of the 2 walks will be used in the analysis.
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24 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Peak exercise oxygen uptake (VO2)
Time Frame: 24 weeks
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Peak VO2 will be measured while performing cycle ergometry exercise.
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24 weeks
|
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Resting heart rate
Time Frame: 24 weeks
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Resting heart rate will be measured prior to participant performing a cycle ergometry exercise test.
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24 weeks
|
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Blood pressure
Time Frame: 24 weeks
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Blood pressure will be measured prior to the participant performing a cycle ergometry exercise test.
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24 weeks
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Balance assessment
Time Frame: 24 weeks
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Balance will be measured using the functional reach assessment and the single leg stance assessment.
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24 weeks
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Health related quality of life (HRQOL)
Time Frame: 24 weeks
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The Medical Outcomes Short Form 36 will be used to measure HRQOL.
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24 weeks
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Cognitive function following 6 months of Tai Chi or sham exercise training
Time Frame: 24 weeks
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Cognitive function will be measured using the Montreal Cognitive Assessment (MoCA) questionnaire (Version 7.1).
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24 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Robert S McKelvie, MD, PhD, Hamilton Health Sciences Corporation
- Study Chair: Heather M Arthur, PhD, McMaster University
- Study Chair: George Heckman, MD, MSc, University of Waterloo
- Study Chair: Noori Akhtar-Danesh, PhD, McMaster University
- Study Chair: Maureen MacDonald, PhD, McMaster University
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NA7343
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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