Cardiovascular Risk Factor Clinical Trial
— ART-BOfficial title:
Independent and Combined Effects of Aerobic and Resistance Training on Blood Pressure
| NCT number | NCT03734146 |
| Other study ID # | 14-330 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | July 15, 2014 |
| Est. completion date | December 19, 2014 |
| Verified date | October 2018 |
| Source | Iowa State University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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.
| Status | Completed |
| Enrollment | 69 |
| Est. completion date | December 19, 2014 |
| Est. primary completion date | December 19, 2014 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 45 Years to 74 Years |
| Eligibility |
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 |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Iowa State University |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in resting blood pressure | resting systolic and diastolic blood pressure | Immediately before and after the 8 week intervention |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
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