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Changes in Adiponectin and Cardiovascular Disease Risk Factors in Overweight Patients

U

University of Isfahan

Status and phase

Completed
Phase 1

Conditions

Cardiac Myosins
Patients
Exercise

Treatments

Other: Experimental
Other: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT02882672
201527898IR

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

20 to 50 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Experimental
Experimental group
Description:
experimental group did 8 weeks exercise training
Treatment:
Other: Experimental
Control
Experimental group
Description:
Control group did not do any exercise training.
Treatment:
Other: Control

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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