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Clinical Trials/NCT02882672
NCT02882672
Completed
Phase 1

Exercise-based Cardiac Rehabilitation

University of Isfahan0 sites60 target enrollmentJanuary 2016

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Exercise
Sponsor
University of Isfahan
Enrollment
60
Primary Endpoint
Effect of Exercise-based cardiac rehabilitation on lipids was measured by ELISA method
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This study aimed to determine if eight-weeks of exercise-based cardiac rehabilitation could improve adiponectin and cardiovascular disease risk factors in overweight coronary heart disease patients. Patients were included in the study if: they were approved to do so following a physical, physiological and psychological test; did not take part in regular physical activity; had stable heart failure for at least 3 months. Exclusion criteria included: a history of surgery within the preceding 4 months; had an unstable angina, acute phase of myocardial infarction, and/or unstable arrhythmia; had obstructive cardiomyopathy, exercise-induced ischemia or arrhythmias, uncontrolled arrhythmias, resting blood pressure more than 200/120 millimeters mercury, aortic stenosis, and/or peripheral artery disease; exercise limitations due to neuromuscular and/or musculoskeletal disease; had any health problems that prevented maximum effort on the treadmill test. Target population included of all patients with a history of myocardial infarction and diagnosis of congestive heart failure who were referred to Isfahan Cardiovascular Research Centre. 60overweight coronary heart disease patients were randomly assigned to either an eight-week, three times weekly exercise group (n=30), or a non-exercising control group (n=30). Exercise sessions took place at 60-85% of maximal heart rate, lasted 45-60 minutes and included a 10-minute warm-up, 40 minutes of aerobic exercises, consisting of stationary cycling, walking and/or jogging, flexibility, balance exercises, and weight-bearing activity and a 10-minute cool-down.

Registry
clinicaltrials.gov
Start Date
January 2016
End Date
June 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Prof.Mehdi Kargarfard

Professor Mehdi Kargarfard

University of Isfahan

Eligibility Criteria

Inclusion Criteria

  • they were approved to do so following a physical, physiological and psychological test; resided and worked in the city of Isfahan; did not take part in regular physical activity; had stable heart failure for at least 3 months.

Exclusion Criteria

  • a history of surgery within the preceding 4 months
  • had an unstable angina, acute phase of myocardial infarction (MI), and/or unstable arrhythmia
  • had obstructive cardiomyopathy, exercise-induced ischemia or arrhythmias, uncontrolled arrhythmias, resting blood pressure more than 200/120 millimeters mercury (mmHg), aortic stenosis, and/or peripheral artery disease
  • exercise limitations due to neuromuscular and/or musculoskeletal disease, such as any type of orthopedic, low back pain, bone fracture of less than 6 months
  • uncontrolled systemic disease, such as DM; were 75 years or older
  • had any health problems that prevented maximum effort on the treadmill test
  • unable to answer the screening questionnaires assessing depression and anxiety.

Outcomes

Primary Outcomes

Effect of Exercise-based cardiac rehabilitation on lipids was measured by ELISA method

Time Frame: up to 8 weeks

Effect of Exercise-based cardiac rehabilitation on Serum levels of adiponectin was measured by ELISA method

Time Frame: up to 8 weeks

Exercise sessions took place at 60-85% of maximal heart rate, lasted 45-60 minutes.

Secondary Outcomes

  • Effect of Exercise-based cardiac rehabilitation on height was measured(up to 8 weks)
  • Effect of Exercise-based cardiac rehabilitation on weight was measured(up to 8 weks)

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