Training Levels Comparison Trial

The University of Alabama at Birmingham logo

The University of Alabama at Birmingham

Status

Withdrawn

Conditions

Myocardial Ischemia
Cardiovascular Diseases
Heart Diseases
Coronary Disease

Treatments

Behavioral: High intensity exercise
Behavioral: Low intensity exercise

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT00000460
R01HL037597 (U.S. NIH Grant/Contract)
49

Details and patient eligibility

About

To determine the effects of high or low intensity long-term exercise conditioning in patients with coronary artery disease.

Full description

BACKGROUND: A vast amount of literature exists on the improvements in work capacity, reduction of risk factors, and an increased feeling of well-being among coronary heart disease patients after physical training programs. Previous observations of short-term training programs which resulted in an increase in physical working capacity have not usually shown a cardiac change. The National Exercise and Heart Disease Project did not show such changes, but the exercise level may have been inadequate. Several other studies suggested that more prolonged and intense training could result in improved cardiac function. DESIGN NARRATIVE: Patients were randomized to high intensity or low intensity long-term exercise groups. Compliance was strengthened by randomizing following a sequence of eligibility visits and after a test period of subject reaction to an exercise program. The primary endpoint was change in exercise ejection fraction at one year. Secondary endpoints included changes in lipid levels, body composition, blood pressure and heart rate measurements, glucose tolerance, quality of life measures, compliance, and progression of disease. Patients were classified into one of four strata based on the documented history of myocardial infarction and resting left ventricular ejection fraction. Within each stratum, patients were assigned in equal numbers to the two intensity levels of exercise intervention. All exercise prescriptions were based on exercise testing of patients maintained on their usual medical regimen including drugs. Patients underwent standardized multistage treadmill exercise testing monitored by Doppler echocardiogram at baseline, just prior to randomization and at the three month, six month, one year and two year visits. Patients participated in the structured group exercise sessions three days per week. Each exercise session was preceded by and ended with a five to fifteen minute warm-up and cool-down session. Each patient was given an exercise prescription that included a 30 minute period of walking or of walking and jogging sequences and 15 minutes of arm-leg bicycle ergometer exercise. Recruitment started in May 1987. The last patient was enrolled in March 1990.

Sex

Male

Ages

30 to 67 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Men, ages 30 to 67, with documented coronary heart disease.

Trial design

0 participants in 2 patient groups

Low intensity exercise
Treatment:
Behavioral: Low intensity exercise
High intensity exercise
Treatment:
Behavioral: High intensity exercise

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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