Skip to content

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

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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01948596
Enrollment
13
Registered
2013-09-23
Start date
2013-10-31
Completion date
2015-05-31
Last updated
2016-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, Depression

Keywords

pregnant women, depression, depressive symptoms, omega-3 fatty acids

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.

Interventions

Sponsors

China Medical University, Taiwan
CollaboratorOTHER
Japan Society for the Promotion of Science (JSPS)
CollaboratorUNKNOWN
University of Toyama
CollaboratorOTHER
Chiba University
CollaboratorOTHER
Tokyo Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
total score of the Hamilton Rating Scale for Depression (HAMD)Twelve weeks

Secondary

MeasureTime frame
total score of HAMD4-6 weeks after childbirth
total scores on the Edinburgh Postnatal Depression Scale (EPDS)Twelve weeks, 4-6 weeks after childbirth
total score of the Beck Depression Inventory Ⅱ(BDI-Ⅱ)Twelve weeks, 4-6 weeks after childbirth
major depressive disorder (MDD) as determined by the depression module of the Mini International Neuropsychiatric Interview (MINI)Twelve weeks, 4-6 weeks after childbirth
omega-3 fatty acids concentrations in erythrocytesTweve 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
oxytocin in plasmatwelve 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
phospholipase A2 in plasmatwelve weeks, 4-6 weeks after childbirth

Other

MeasureTime frame
gestational ageat childbirth
gestational diabetes mellitus4-6 weeks after childbirth
gestational hypertension or preeclampsia4-6 weeks after childbirth
induced labourat childbirth
estimated blood lossat childbirth
cesarean sectionat childbirth
operative vaginal deliveryat childbirth
birthweightat childbirth
one minute apgar4-6 weeks after childbirth
5-minute apgar4-6 weeks after childbirth
neonatal intensive care unit admission4-6 weeks after childbirth
cholesteroltwelve weeks and 4-6 weeks after childbirth

Countries

Japan, Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026