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
| Type | Name | Description |
|---|---|---|
| DRUG | Motherwell | The 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.