Heart Failure. Congestive heart disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria:The age range40-70 years; with II, III grade heart failure ; patient with the most important aggravating factors including kidney, lung, diabetes and hypertension difficulties Exclusion criteria: :Exacerbation of heart failure symptoms; arrhythmia ; ischemic ; HTN crisis; Psychiatric problem;orthopedic problem; speech problem; hearing problem
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lung volume In the intervention group. Timepoint: Before and after 8 weeks of exercise training. Method of measurement: spirometry.;Lung Volume In the control group. Timepoint: Before and 8 weeks After the start of the study. Method of measurement: Spirometry.;Lung capacity In the intervention group. Timepoint: Before and 8 weeks after exercise training. Method of measurement: spirometry.;Function and structure of the heart include: LVEF left ventricular fraction (%), systolic ending volume (ESV) and diastolic end volume (EDV). Timepoint: before and after 8 weeks of exercise training. Method of measurement: Echocardiogaphy.;Heart Rate. Timepoint: before and after of 8 week. Method of measurement: Pulseoximeter.;Blood Pressure. Timepoint: before and after of 8 weeks of exercise training. Method of measurement: pressure indicator.;Cr(Creatine Blood). Timepoint: before and after 8 weeks of exercise training. Method of measurement: Blood Test.;Potency function. Timepoint: before and after 8 weeks of exercise training. Method of measurement: 6-minute test.;HDL, LDL. Timepoint: before and after 8 weeks of exercise training. Method of measurement: Blood test.;BS? HbA1C. Timepoint: before and after 8 weeks of exercise training. Method of measurement: Blood Test.;Lung capacity In the controlgroup. Timepoint: before and 8 week After the start of the study. Method of measurement: Spirometry.;Blood Pressure in the control group. Timepoint: before and 8 week After the start of the study. Method of measurement: pressure indicator.;Cr(cratinine Blood) in the control group. Timepoint: before and 8 week After the start of the study. Method of measurement: Blood Test.;Heart rate in the control group. Timepoint: before and 8 week After the start of the study. Method of measurement: pulseoximetry.;Potency function in the control group. Timepoint: before and 8 week After the start of the study. Method of measurement: 6 minute test.;HDL, LDL Blood in the control group. Timepoint: before | — |
Secondary
| Measure | Time frame |
|---|---|
| Cardiac arrhythmia. Timepoint: During the exercise. Method of measurement: manitoring.;Ischemia. Timepoint: During the exercise. Method of measurement: manitoring.;HTN crisis. Timepoint: By indication symptoms. Method of measurement: pressure indicator. | — |
Countries
Iran (Islamic Republic of)
Contacts
Guilan Guilan University of Medical Sciences