Clinical Trials Directory

Trials / Completed

CompletedNCT02466087

Role of Magnesium Supplementation in the Treatment of Depression

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
126 (actual)
Sponsor
University of Vermont · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this project is to test the hypothesis that magnesium supplementation will decrease depressive symptoms in adults. This study takes place over 12 consecutive weeks. While the investigators will follow the volunteers for the full 12 weeks volunteers will only take magnesium supplements for 6 consecutive weeks. Volunteers will be randomly assigned to start the supplement at week 1 or week 7. Volunteers will take two supplement two times a day for a total of 248 mg elemental magnesium daily in the form of magnesium chloride. This amount of magnesium is less than the tolerable upper limit of 350 mg per day. The supplements will be provided. Volunteers will be asked to maintain their normal diet for the 12 weeks of the study. The primary outcome measure is the PHQ-9 questionnaire, a validated measure of depression. Secondary measures include the GAD-7 for Anxiety and side effects.

Conditions

Interventions

TypeNameDescription
DRUGMg ClFour supplements a day for 6 weeks.

Timeline

Start date
2015-05-01
Primary completion
2016-05-01
Completion
2016-12-01
First posted
2015-06-09
Last updated
2019-05-08
Results posted
2019-05-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02466087. Inclusion in this directory is not an endorsement.