Effect of combined training in treatment of primary hypertensio
- Conditions
- Primary Hypertension.Essential (primary) hypertension
- Registration Number
- IRCT20190317043080N1
- Lead Sponsor
- The University of Birjand
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 60
Have primary hypertension and at least one year has passed since their illness
The range of systolic blood pressure should be in the range of 140-159 mmHg and diastolic blood pressure should be in the range of 99-90 mmHg
Do not have a history of doing regular exercise training in the six months leading up to the research
Do not have any history of heart surgery
Do not have diabetes, fatty liver, hypothyroidism or hyperthyroidism, anemia and kidney disease
Do not have a history of myocardial infarction, heart attack, cardiac arrhythmia, ischemic disease, or unstable angina
There is a problem in the bone, muscle and joints that prevent doing exercise
The use of calcium channel blockers such as verapamil, amlodipine, diltiazem
Smoking, drug addiction and alcohol consumption
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Superoxide dismutase enzyme activity. Timepoint: At the beginning of the study (before the intervention), at the end of the study (after the intervention). Method of measurement: Calorimetric assay (superoxide dismutase kit).;Fibrinogen. Timepoint: At the beginning of the study (before the intervention), at the end of the study (after the intervention). Method of measurement: Enzyme – Linked ImmunoSorbent Assay (ELISA kit for fibrinogen).
- Secondary Outcome Measures
Name Time Method