Assessment of combined exercise training effect in men with primary hypertensio
- Conditions
- Primary hypertension.Essential (primary) hypertension
- Registration Number
- IRCT20160317027092N2
- Lead Sponsor
- Birjand University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 60
Age range between 30-70 years is allowed.
According to a specialist doctor's diagnosis, they have primary hypertension and at least one year has passed since their illness
Doctors' permission to participate in an exercise program and no need for a specific drug (calcium channel blockers such as verapamil that significantly decrease TXNIP in Langerhans beta cells) (Poudel & Kafle, 2017), at least until Completion of the research period (10 weeks) is required
Do not take more than one type of antihypertensive pill daily
Their minimum systolic blood pressure was 140 mmHg and diastolic blood pressure was 90 mmHg.
They do not have a history of regular exercise in the six months leading up to the time of the study
People should not participate in specific weight loss programs
Do not have diabetes, fatty liver, Hypothyroidism or hyperthyroidism, anemia (Hb <10 g / dl) and kidney disease (> 1.5 mg / dl creatinine) and Do not have a history of Myocardial infarction, heart attack, cardiac arrhythmia Also do not have ischemic heart disease or unstable angina (Farinatti et al., 2016). This informationwill be obtained through the medical records of individuals.
They have no history of any heart surgery
Having bone, muscles, and joints problems that prevent exercise.
Have a blood pressure higher than 180 mmHg.
Take calcium channel blocker drugs such as verapamil, amlodipine, diltiazem.
Smoking or addiction to any drug or alcohol (Moraes et al., 2012).
Participate in any other exercise program (recreational or professional) while conducting research.
Have no interest in participating in a sports activity program.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method