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Clinical Trials/NCT03734146
NCT03734146
Completed
Not Applicable

Independent and Combined Effects of Aerobic and Resistance Training on Blood Pressure

Iowa State University0 sites69 target enrollmentJuly 15, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Risk Factor
Sponsor
Iowa State University
Enrollment
69
Primary Endpoint
Change in resting blood pressure
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

We compared the effects of 8 weeks of aerobic exercise only, resistance exercise only, or a combination of both on blood pressure in overweight or obese middle-aged adults with elevated blood pressure. Participants engaged in supervised exercise sessions 3 times per week for 60 minutes each session. Outcomes were assessed at baseline and after the 8-week intervention. Extra-intervention physical activity and diet were also assessed.

Registry
clinicaltrials.gov
Start Date
July 15, 2014
End Date
December 19, 2014
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Systolic/diastolic blood pressure of 120-159/80-99 mm Hg
  • Non-smoking
  • Overweight or obese, with a body mass index of 25-40 kg/m2
  • Inactive--not meeting the aerobic or resistance physical activity guidelines, which means engaging in less than 150 minutes/wk of moderate intensity aerobic exercise and less than 2 days per week of resistance training over the past 3 months.

Exclusion Criteria

  • Unstable coronary heart disease or decompensated heart failure
  • Severe pulmonary hypertension or aortic stenosis
  • Acute myocarditis, endocarditis, pericarditis, or aortic dissection
  • Other medical condition that is life-threatening or that can interfere or be aggravated by the exercise training such as cancer, uncontrolled diabetes, severe pain or mobility limitations.
  • Premenopausal women or postmenopausal women taking hormonal replacement therapy
  • Pregnant women or anticipated pregnancy via IVF or other medical procedures during the course of the intervention

Outcomes

Primary Outcomes

Change in resting blood pressure

Time Frame: Immediately before and after the 8 week intervention

resting systolic and diastolic blood pressure

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