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LungVITamin D and OmegA-3 Trial (lungVITAL) (lungVITAL)

Primary Purpose

COPD, Asthma, Pulmonary Function

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Vitamin D3
fish oil
Vitamin D3 placebo
Fish oil placebo
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for COPD focused on measuring COPD, asthma, pulmonary function, pneumonia

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers
  • This study is open to all VITAL participants (NCT 01169259). Population includes men 50 years of age or older and women 55 years of age or older in the United States
  • Participants who live in selected metropolitan areas of the U.S. (where we set up the infrastructure for clinic or home visits), are eligible for pulmonary function measurements.

Sites / Locations

  • Brigham and Women's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Vitamin D3 + fish oil

Vitamin D3 + fish oil placebo

Vitamin D3 placebo + fish oil

Vitamin D3 placebo + fish oil placebo

Arm Description

Dietary Supplement: vitamin D3 Drug: omega-3 fatty acids (fish oil)

Dietary Supplement: vitamin D3 Dietary Supplement: fish oil placebo

Drug: omega-3 fatty acids (fish oil) Dietary Supplement: vitamin D3 placebo

Dietary Supplement: vitamin D3 placebo Dietary Supplement: fish oil placebo

Outcomes

Primary Outcome Measures

COPD exacerbations in the past year over the course of the study
Baseline respiratory symptom status, respiratory disease diagnoses, and COPD (chronic obstructive pulmonary disease) exacerbations in the past year are measured pre-randomization and annually during follow-up.
Airflow obstruction/change in pulmonary function
In a sub-group of study participants pulmonary function will be measured pre-randomization and after 2 years of follow-up
Pneumonia in the past year over the course of the study
Pneumonia in the past year (overall and in those with COPD and asthma) is measured pre-randomization and annually during follow-up.

Secondary Outcome Measures

Asthma exacerbations and asthma control in the past year over the course of the study
Participants who report an asthma diagnosis are asked questions related to respiratory illness exacerbations and asthma control annually during follow-up.

Full Information

First Posted
October 25, 2012
Last Updated
August 11, 2021
Sponsor
Brigham and Women's Hospital
Collaborators
Harvard School of Public Health (HSPH)
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1. Study Identification

Unique Protocol Identification Number
NCT01728571
Brief Title
LungVITamin D and OmegA-3 Trial (lungVITAL)
Acronym
lungVITAL
Official Title
LungVITamin D and OmegA-3 Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 2010 (undefined)
Primary Completion Date
November 10, 2018 (Actual)
Study Completion Date
February 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
Harvard School of Public Health (HSPH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The VITamin D and OmegA-3 TriaL (VITAL; NCT 01169259) is an ongoing randomized clinical trial in 25,871 U.S. men and women investigating whether taking daily dietary supplements of vitamin D3 (2000 IU) or omega-3 fatty acids (Omacor® fish oil, 1 gram) reduces the risk of developing cancer, heart disease, and stroke in people who do not have a prior history of these illnesses. This ancillary study is being conducted among participants in VITAL and will examine whether vitamin D or fish oil reduces respiratory morbidity, including COPD and asthma exacerbations, the risk of pneumonia, and airflow obstruction/decline of pulmonary function; and whether either of these interventions improves asthma control.
Detailed Description
Chronic obstructive lung disease (COPD) and pneumonia are leading causes of death in United States and worldwide. COPD, which is also a significant source of disability, is increasing in prevalence. Approximately 14 million adults have asthma, which leads to approximately 12 million missed work days per year in the United States. In adults, COPD and asthma often coexist. Treatment options for COPD are limited, and prevalence of vitamin D deficiency is high. COPD lung disease (COPD, asthma, airflow obstruction), and most COPD additional co-morbidities responsible for COPD progression (e.g., respiratory infections/pneumonia, muscle weakness, cardiac failure) may benefit from vitamin D supplementation therapy, but this requires rigorous testing. Marine omega-3 fatty acids work through different pathways from vitamin D to affect inflammation. Observational studies and clinical trials suggest that consumption of fish and/or fish oil may protect against COPD, asthma or pneumonia, but the data are not consistent. Thus, there is a compelling need for a clinical trial to evaluate the potential benefits or risks of vitamin D and fish oil supplementation on COPD and asthma exacerbations, airflow obstruction and decline of lung function, and risk of pneumonia. The primary outcomes of interest in Lung VITAL are COPD exacerbations; airflow obstruction and decline of pulmonary function; and pneumonia. Asthma exacerbations and asthma control are secondary outcomes. A tertiary goal is to assess whether the effects of the interventions differ by baseline dietary intake or baseline blood levels of the nutrients. Depending on the primary outcome, Lung VITAL will be conducted among all participants in VITAL (NCT 01169259), or in subsets of the VITAL population who were followed by detailed respiratory questionnaire and/or lung function testing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COPD, Asthma, Pulmonary Function, Pneumonia
Keywords
COPD, asthma, pulmonary function, pneumonia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
25871 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D3 + fish oil
Arm Type
Active Comparator
Arm Description
Dietary Supplement: vitamin D3 Drug: omega-3 fatty acids (fish oil)
Arm Title
Vitamin D3 + fish oil placebo
Arm Type
Active Comparator
Arm Description
Dietary Supplement: vitamin D3 Dietary Supplement: fish oil placebo
Arm Title
Vitamin D3 placebo + fish oil
Arm Type
Active Comparator
Arm Description
Drug: omega-3 fatty acids (fish oil) Dietary Supplement: vitamin D3 placebo
Arm Title
Vitamin D3 placebo + fish oil placebo
Arm Type
Placebo Comparator
Arm Description
Dietary Supplement: vitamin D3 placebo Dietary Supplement: fish oil placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3
Other Intervention Name(s)
Vitamin D3 (cholecalciferol), 2000 IU per day. Other Name: cholecalciferol
Intervention Type
Dietary Supplement
Intervention Name(s)
fish oil
Other Intervention Name(s)
Omacor; 1 g per day as a fish oil capsule, containing 840 milligrams of marine omega-3 fatty acids (460 mg of eicosapentaenoic acid [EPA] and 380 mg of docosahexaenoic acid [DHA]).
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3 placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish oil placebo
Primary Outcome Measure Information:
Title
COPD exacerbations in the past year over the course of the study
Description
Baseline respiratory symptom status, respiratory disease diagnoses, and COPD (chronic obstructive pulmonary disease) exacerbations in the past year are measured pre-randomization and annually during follow-up.
Time Frame
at baseline (before randomization), 1-year, 2-year, 3-year,4-year, 5-year
Title
Airflow obstruction/change in pulmonary function
Description
In a sub-group of study participants pulmonary function will be measured pre-randomization and after 2 years of follow-up
Time Frame
pre-randomization and after 2 years follow-up
Title
Pneumonia in the past year over the course of the study
Description
Pneumonia in the past year (overall and in those with COPD and asthma) is measured pre-randomization and annually during follow-up.
Time Frame
at baseline (before randomization), 1-year, 2-year, 3-year,4-year, 5-year
Secondary Outcome Measure Information:
Title
Asthma exacerbations and asthma control in the past year over the course of the study
Description
Participants who report an asthma diagnosis are asked questions related to respiratory illness exacerbations and asthma control annually during follow-up.
Time Frame
at baseline (before randomization), 1-year, 2-year, 3-year,4-year, 5-year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
This study is open to all VITAL participants (NCT 01169259). Population includes men 50 years of age or older and women 55 years of age or older in the United States Participants who live in selected metropolitan areas of the U.S. (where we set up the infrastructure for clinic or home visits), are eligible for pulmonary function measurements.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Diane R Gold, MD, MPH
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26784651
Citation
Gold DR, Litonjua AA, Carey VJ, Manson JE, Buring JE, Lee IM, Gordon D, Walter J, Friedenberg G, Hankinson JL, Copeland T, Luttmann-Gibson H. Lung VITAL: Rationale, design, and baseline characteristics of an ancillary study evaluating the effects of vitamin D and/or marine omega-3 fatty acid supplements on acute exacerbations of chronic respiratory disease, asthma control, pneumonia and lung function in adults. Contemp Clin Trials. 2016 Mar;47:185-95. doi: 10.1016/j.cct.2016.01.003. Epub 2016 Jan 16.
Results Reference
derived

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LungVITamin D and OmegA-3 Trial (lungVITAL)

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