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The Synchronized Trial on Expectant Mothers With Depressive Symptoms by Omega-3 PUFAs (SYNCHRO): Open Trial

Phase 2
Completed
Conditions
Pregnancy
Depression
Interventions
Dietary Supplement: Omega-3 polyunsaturated fatty acids
Registration Number
NCT01948596
Lead Sponsor
Tokyo Medical University
Brief Summary

The present study aims to examine the efficacy and safety of omega-3 polyunsaturated fatty acids for pregnant women with depressive symptoms.

Detailed Description

Maternal depression can have a significant harmful influence on both mothers and children. Considering the possibility of adverse effects of antidepressants and previous meta-analyses showing the positive effects of omega-3 polyunsaturated fatty acids (PUFAs) supplementation in reducing depressive symptoms, omega-3 PUFAs may provide a safe strategy. The investigators evaluate efficacy and safety of omega-3 PUFAs for pregnant women with depressive symptoms.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
13
Inclusion Criteria
  1. pregnant women aged 20 years or older
  2. between 12-24 weeks gestation
  3. a Japanese conversational ability in Japan site or a Mandarin conversational ability in Taiwan site to understand the scope of the present trial and to provide written consent for study participation
  4. planned to return to the hospital for checkup at 4-6 weeks after childbirth
  5. an Edinburgh Postnatal Depression Scale (EPDS) score is 9 or more
  6. to have good physical health judged by obstetricians.
Exclusion Criteria
  1. history and current suspicion of psychosis or bipolar I disorder or substance-related disorder or eating disorder or personality disorder
  2. the item of EPDS concerning suicide ideation is 2 or more
  3. other serious psychiatric symptoms such as self-harm behavior or in need of rapid psychiatric treatment
  4. difficult to expect a normal birth (ex: fetal malformation etc.)
  5. having a history of bleeding disorder such as von Willebrand's Disease
  6. regular treatment with aspirin or warfarin within the last 3 months
  7. a smoking habit of ≥40 cigarettes per day
  8. regular treatment with ethyl icosapentate or regular consumption of omega-3 PUFA supplements within the last 3 months
  9. a habit of eating fish ≥4 times per week.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Omega-3 polyunsaturated fatty acidsOmega-3 polyunsaturated fatty acids1200mg eicosapentaenoic acid (EPA) and 600mg docosahexaenoic acid (DHA) daily
Primary Outcome Measures
NameTimeMethod
total score of the Hamilton Rating Scale for Depression (HAMD)Twelve weeks
Secondary Outcome Measures
NameTimeMethod
major depressive disorder (MDD) as determined by the depression module of the Mini International Neuropsychiatric Interview (MINI)Twelve weeks, 4-6 weeks after childbirth
oxytocin in plasmatwelve weeks, 4-6 weeks after childbirth
total score of the Beck Depression Inventory Ⅱ(BDI-Ⅱ)Twelve weeks, 4-6 weeks after childbirth
total score of HAMD4-6 weeks after childbirth
total scores on the Edinburgh Postnatal Depression Scale (EPDS)Twelve weeks, 4-6 weeks after childbirth
omega-3 fatty acids concentrations in erythrocytesTweve weeks, 4-6 weeks after childbirth
TNF-alpha in plasmatwelve weeks, 4-6 weeks after childbirth
IL-1 beta in plasmatwelve weeks, 4-6 weeks after childbirth
brain-derived neurotrophic factor (BDNF) in serumTwelve weeks, 4-6 weeks after childbirth
IF-6 in plasmatwelve weeks, 4-6 weeks after childbirth
phospholipase A2 in plasmatwelve weeks, 4-6 weeks after childbirth

Trial Locations

Locations (3)

Toda Maternity Hospital

🇯🇵

Toda, Saitama, Japan

China Medical University

🇨🇳

Taichung, Taiwan

Tokyo Medical University

🇯🇵

Shinjuku-ku, Tokyo, Japan

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