Mechanism of the Blood Pressure Lowering Effect of the DASH Dietary Pattern
NCT ID: NCT01017484
Last Updated: 2013-04-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2007-07-31
2009-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
DOUBLE
Study Groups
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DASH
The Dietary Approaches to Stop Hypertension Dietary pattern.
DASH, Control
controlled feeding of either the DASH dietary pattern or a typical American diet at isocaloric level.
Control
The typical American diet as estimated from the NHANES survey.
DASH, Control
controlled feeding of either the DASH dietary pattern or a typical American diet at isocaloric level.
Interventions
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DASH, Control
controlled feeding of either the DASH dietary pattern or a typical American diet at isocaloric level.
Eligibility Criteria
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Inclusion Criteria
2. Age ≥22 years, and
3. Willing to eat at least one on-site meal/day, five days/week, and willing to eat study diets and nothing else for the 3 weeks of controlled feeding.
Exclusion Criteria
2. Currently on cancer chemotherapy or with evidence of active malignancy or radiation therapy within past six months,
3. History of CVD event (MI, CABG, angioplasty, symptomatic ischemic heart disease, or stroke),
4. Clinical diagnosis of congestive heart failure,
5. Current diagnosis of diabetes and treatment for diabetes with oral medication or insulin,
6. Body mass index \> 45 Kg/m2,
7. DASH MECHANISM staff or household member of DASH MECHANISM staff,
8. Using Medications including BP lowering drugs within the last three months, using lithium,insulin or oral diabetes medications, oral corticosteroids, unstable doses of psychotropics or phenothiazines, antacids or nutritional supplements unless they can be discontinued, or weight reducing medications;
9. Consumption of more than 14 alcoholic drinks per week;
10. Investigator discretion for safety or compliance reasons;
11. Inability to provide reliable BP \& vascular functions measurements;
12. Planning to leave the area prior to the anticipated end of the intervention period;
13. Pregnant, planning a pregnancy prior to the end of intervention, or breast feeding;
14. Significant food allergies, preferences, or dietary requirements that would interfere with diet adherence; and
15. Subjects taking medications for erectile dysfunction.
22 Years
ALL
Yes
Sponsors
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American Heart Association
OTHER
Duke University
OTHER
Responsible Party
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Principal Investigators
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Pao-Hwa Lin, PhD
Role: PRINCIPAL_INVESTIGATOR
Duke University
Other Identifiers
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AHA 0755460U
Identifier Type: OTHER
Identifier Source: secondary_id
Pro00001236
Identifier Type: -
Identifier Source: org_study_id
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