Blood Pressure Clinical Trial
Official title:
Daily Incorporation of Blueberries Into a Diet Favorably Improves Vascular Function and Lowers Aortic Blood Pressure in Postmenopausal Women With Pre- and Stage 1-hypertension.
Verified date | January 2015 |
Source | Florida State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
Cardiovascular disease (CVD) continues to be the leading cause of death in the U.S.
Americans have been more concerned about their blood cholesterol levels and dietary
cholesterol intakes rather than their overall cardiovascular health risk factors leading to
CVD such as hypertension, vascular dysfunction, inadequate consumption of fruits and
vegetables and physical activity. Statistics show that approximately 91% of individuals with
CVD have vascular dysfunction which is attributed to endothelial and autonomic dysfunction
leading to increased arterial stiffness.
The investigators long-term goal is to provide feasible and effective dietary ways for pre-
and stage 1- hypertensive individuals to normalize their blood pressure (BP), improve
vascular function and thereby reducing their cardiovascular risk and enhancing the quality
of life. Blueberries are a rich source of phenolic compounds and these compounds may play an
important role in promoting cardiovascular health. Considering the strong possibility that
phytochemicals present in blueberry work additively or synergistically, it would be ideal to
investigate the cardioprotective effects of blueberry as a whole. The investigators overall
objective to bring forth evidence that blueberry consumption will reduce BP and
cardiovascular risk factors including endothelial dysfunction, arterial stiffness, and
autonomic dysfunction in pre- and stage 1-hypertensive postmenopausal women. The
investigators hypothesize that blueberry supplementation will improve vascular function and
will lower blood pressure in postmenopausal women with pre-hypertension. The findings of
this study will provide a foundation for disseminating feasible, safe approaches for
preventing and combating hypertension at its early stage which does not require drug
therapy.
Status | Completed |
Enrollment | 48 |
Est. completion date | January 2014 |
Est. primary completion date | March 2013 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 45 Years to 65 Years |
Eligibility |
Inclusion Criteria: - 40 women (1 to 10 years after natural menopause or bilateral oophorectomy) 45-65 years of age. - Seated blood pressure = 130/85 mm Hg but = 160/90 mm Hg. Exclusion Criteria: - Blood pressure >160/100 mmHg - Taking insulin - Cardiovascular disease - Active cancer - Asthma - Glaucoma - Thyroid disease - Kidney disease - Liver disease - Pancreatic disease - Enrollment in a weight loss program - Heavy smokers (>20 cigarettes per day) |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | The Department of Nutrition, Food, and Exercise Sciences, Florida State University | Tallahassee | Florida |
Lead Sponsor | Collaborator |
---|---|
Florida State University | U.S. Highbush Blueberry Council |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Blood Pressure | By measuring aortic blood pressure at rest and during physiological stress (handgrip exercise and post-exercise muscle ischemia). | 8 weeks | No |
Secondary | Autonomic Control of Blood Pressure | By measuring blood pressure variability and baroreflex sensitivity at rest and during physiological stress. | 8 weeks | No |
Secondary | Autonomic Control of Heart Rate | By measuring heart rate variability at rest and during physiological stress. | 8 weeks | No |
Secondary | Endothelial Function | By measuring markers of vascular inflammation (adiponectin, leptin, endothelin-1, angiotensin II and 8-isoprostane). | 8 week | No |
Secondary | Inflammation | By measuring a marker of inflammation (tumor necrosis factor-a [TNF-a]). | 8 weeks | No |
Secondary | Oxidative Stress | By measuring markers of oxidative stress (superoxide dismutase [SOD], nitrate/nitrite [NOx], ET-1, angiotensin II, 8-isoprostane, MDA, and oxidized LDL). | 8 weeks | No |
Secondary | Arterial Stiffness | By measuring the augmentation index and arterial stiffness at rest and during physiological stress (handgrip exercise and post-exercise muscle ischemia). | 8 Week | No |
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