The Synchronized Trial on Expectant Mothers With Depressive Symptoms by Omega-3 PUFAs (SYNCHRO): Open Trial
- Conditions
- PregnancyDepression
- 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
- pregnant women aged 20 years or older
- between 12-24 weeks gestation
- 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
- planned to return to the hospital for checkup at 4-6 weeks after childbirth
- an Edinburgh Postnatal Depression Scale (EPDS) score is 9 or more
- to have good physical health judged by obstetricians.
- history and current suspicion of psychosis or bipolar I disorder or substance-related disorder or eating disorder or personality disorder
- the item of EPDS concerning suicide ideation is 2 or more
- other serious psychiatric symptoms such as self-harm behavior or in need of rapid psychiatric treatment
- difficult to expect a normal birth (ex: fetal malformation etc.)
- having a history of bleeding disorder such as von Willebrand's Disease
- regular treatment with aspirin or warfarin within the last 3 months
- a smoking habit of ≥40 cigarettes per day
- regular treatment with ethyl icosapentate or regular consumption of omega-3 PUFA supplements within the last 3 months
- a habit of eating fish ≥4 times per week.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Omega-3 polyunsaturated fatty acids Omega-3 polyunsaturated fatty acids 1200mg eicosapentaenoic acid (EPA) and 600mg docosahexaenoic acid (DHA) daily
- Primary Outcome Measures
Name Time Method total score of the Hamilton Rating Scale for Depression (HAMD) Twelve weeks
- Secondary Outcome Measures
Name Time Method 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 plasma twelve 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 HAMD 4-6 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 erythrocytes Tweve weeks, 4-6 weeks after childbirth TNF-alpha in plasma twelve weeks, 4-6 weeks after childbirth IL-1 beta in plasma twelve weeks, 4-6 weeks after childbirth brain-derived neurotrophic factor (BDNF) in serum Twelve weeks, 4-6 weeks after childbirth IF-6 in plasma twelve weeks, 4-6 weeks after childbirth phospholipase A2 in plasma twelve 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