Vitamin D and Omega-3 Hypertension Trial (VITAL Hypertension)
|ClinicalTrials.gov Identifier: NCT01653678|
Recruitment Status : Active, not recruiting
First Posted : July 31, 2012
Last Update Posted : January 19, 2018
|Condition or disease||Intervention/treatment||Phase|
|Hypertension||Dietary Supplement: Vitamin D-3 (cholecalciferol), 2000 IU Drug: Omega-3 fatty acids (fish oil) Dietary Supplement: Vitamin D placebo Drug: Fish oil placebo||Not Applicable|
The human toll of hypertension is staggering, and effective preventive measures are needed. Studies suggest that inadequate vitamin D and omega-3 fatty acid levels may be involved in the development of hypertension through multiple pathways. Results from several small clinical trials suggest that these agents may have blood pressure lowering effects, however, larger trials using higher doses of both vitamin D and omega-3 fatty acids for the prevention of hypertension among people with normal blood pressure levels are lacking. The VITamin D and OmegA-3 TriaL (VITAL) provides a cost-effective setting to examine the effects of both study agents on changes in blood pressure and new diagnoses of hypertension.
VITAL Hypertension will test the following hypotheses: (1) whether vitamin D and fish oil supplementation lowers 24-hour blood ambulatory blood pressure (ABP) compared to placebo in a subcohort of 1,000 participants; (2) whether vitamin D and fish oil supplementation reduces the risk of incident hypertension compared to placebo among all randomized VITAL participants without baseline hypertension; and (3) whether vitamin D and fish oil supplementation favorably change hypertension-related biomarkers that are potential mechanisms linking vitamin D and omega-3 fatty acids with hypertension compared to placebo.
A representative subcohort of 1,000 VITAL participants without hypertension from selected major metropolitan areas throughout the US will be invited to participate in home-based study visits at baseline and 2 years follow-up. During these visits, participants will be asked to wear monitors to record 24-hour ABP measurements, provide fasting bloods, spot urine samples, and other clinical measurements. The visits will be conducted by Examination Management Services, Inc. (EMSI), a nationally based, clinical services provider. We will compare 2-year changes in ABP among those randomized to vitamin D and omega-3 fatty acid supplements versus those randomized to placebo. In addition, we will assess the 2-year changes in levels of clinically and mechanistically relevant biomarkers of hypertension compared the 2 treatment groups.
New diagnoses of hypertension among all VITAL participants will be ascertained on annual follow-up questionnaires. To strengthen our classification of hypertension status, we will supplement our questionnaire data with annual updates of hypertension information based upon outpatient diagnostic codes and medication prescription usage from the Centers for Medicare & Medicaid Services (CMS) database. Incidence of hypertension among those assigned to each active agent versus placebo will be compared.
In addition, baseline blood samples from 1,000 participants with new diagnoses of hypertension will be compared with those from 2,000 participants without hypertension to determine whether the effect of vitamin D and/or omega-3 fatty acid supplements on the incidence of hypertension is modified by baseline plasma levels of vitamin D or omega-3 fatty acids.
Results from VITAL Hypertension will provide important evidence to support or refute the potential preventive roles of vitamin D and omega-3 fatty acids on blood pressure and the development of hypertension.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||25875 participants|
|Intervention Model:||Factorial Assignment|
|Masking:||Triple (Participant, Investigator, Outcomes Assessor)|
|Official Title:||Effect of Vitamin D and Omega-3 Fatty Acids on Blood Pressure and Hypertension|
|Study Start Date :||November 2011|
|Estimated Primary Completion Date :||December 2018|
|Estimated Study Completion Date :||December 2018|
|Active Comparator: Vitamin D + fish oil||
Dietary Supplement: Vitamin D-3 (cholecalciferol), 2000 IU
Other Name: cholecalciferolDrug: Omega-3 fatty acids (fish oil)
Omacor, 1 capsule per day. Each capsule of Omacor contains 840 milligrams of marine omega-3 fatty acids (465 mg of eicosapentaenoic acid [EPA] and 375 mg of docosahexaenoic acid [DHA])
|Active Comparator: Vitamin D + fish oil placebo||
Dietary Supplement: Vitamin D-3 (cholecalciferol), 2000 IU
Other Name: cholecalciferolDrug: Fish oil placebo
|Active Comparator: Vitamin D placebo + fish oil||
Drug: Omega-3 fatty acids (fish oil)
Omacor, 1 capsule per day. Each capsule of Omacor contains 840 milligrams of marine omega-3 fatty acids (465 mg of eicosapentaenoic acid [EPA] and 375 mg of docosahexaenoic acid [DHA])Dietary Supplement: Vitamin D placebo
|Placebo Comparator: Vitamin D placebo + fish oil placebo||Dietary Supplement: Vitamin D placebo Drug: Fish oil placebo|
- Change in blood pressure [ Time Frame: Two years ]Change in 24-hour ambulatory blood pressure measurements among a subcohort of approximately 1,000 participants.
- Incident hypertension [ Time Frame: 5 years ]Incidence of hypertension in the overall VITAL trial cohort.
- Changes in 25-hydroxy-vitamin D levels [ Time Frame: 2 years ]Changes in a subcohort of approximately 1,000 participants.
- Changes in fatty acid levels [ Time Frame: 2 years ]Changes in a subcohort of approximately 1,000 participants
- Changes in biomarkers related to blood pressure [ Time Frame: 2 years ]Changes in a subcohort of approximately 1,000 participants
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01653678
|United States, Massachusetts|
|Brigham and Women's Hospital|
|Boston, Massachusetts, United States, 02215|
|Principal Investigator:||Howard D. Sesso, ScD, MPH||Brigham and Women's Hospital|
|Principal Investigator:||John P. Forman, MD||Brigham and Women's Hospital|