Clinical Trials Directory

Trials / Completed

CompletedNCT02073175

Development of Dietary Supplements for Mood Symptoms in Postpartum

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
28 (actual)
Sponsor
Centre for Addiction and Mental Health · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether a dietary supplement (DS) is effective in protecting against sad mood in postpartum.

Detailed description

The specific aim of this open-label study is to assess whether the proposed dietary supplement can reduce the intensity of sadness in women vulnerable to sadness (day-5 postpartum women and women within the first 18 months postpartum with crying spells).

Conditions

Interventions

TypeNameDescription
DRUGMotherwellThe interventions involves a dietary supplement called Motherwell, at current stage, to reduce the intensity of sadness in women vulnerable to sadness.

Timeline

Start date
2014-02-01
Primary completion
2016-04-01
Completion
2016-04-01
First posted
2014-02-27
Last updated
2016-04-13

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02073175. Inclusion in this directory is not an endorsement.