Vitamin D for COVID-19 Trial

NCT04536298 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 2024

Last updated 2025-09-24

No results posted yet for this study

Summary

The Vitamin D for COVID-19 Trial (VIVID) is a randomized, placebo-controlled clinical trial in 2024 men and women from across the U.S. and Mongolia to investigate whether taking a daily dietary supplement of vitamin D vs. placebo for 4 weeks reduces the rate of seeking healthcare for symptoms or concerns related to COVID-19 in participants recently diagnosed with COVID-19, and reduces the risk of infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in household contacts of individuals with newly diagnosed COVID-19.

Conditions

Interventions

DIETARY_SUPPLEMENT

vitamin D

Vitamin D softgel capsules; each capsule contains 3200 IU of vitamin D3. Three capsules per day (9600 IU/day) will be taken on days 1 and 2, and one capsule per day (3200 IU/day) will be taken on days 3 through 28

DIETARY_SUPPLEMENT

Placebo

Placebo softgel capsules. Three capsules per day will be taken on days 1 and 2, and one capsule per day will be taken on days 3 through 28

Sponsors & Collaborators

  • Harvard Medical School (HMS and HSDM)

    collaborator OTHER
  • Harvard School of Public Health (HSPH)

    collaborator OTHER
  • Fenway Health and Beth Israel Deaconess Medical Center

    collaborator UNKNOWN
  • Tishcon Corporation

    collaborator UNKNOWN
  • Takeda

    collaborator INDUSTRY
  • Quest Diagnostics-Nichols Insitute

    collaborator INDUSTRY
  • Laboratory Corporation of America

    collaborator INDUSTRY
  • Trialfacts

    collaborator UNKNOWN
  • Karolinska Institutet

    collaborator OTHER
  • Philanthropic donations

    collaborator UNKNOWN
  • Brigham and Women's Hospital

    lead OTHER

Principal Investigators

  • JoAnn E Manson, MD, DrPH · Brigham and Women's Hospital

  • Rui Wang, PhD · Harvard Medical School (HMS and HSDM)

  • Davaasambuu Ganmaa, PhD · Harvard School of Public Health (HSPH)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-12-28
Primary Completion
2024-07-01
Completion
2024-07-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04536298 on ClinicalTrials.gov