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Taking people in TaiwanNo phase

Omega-3 supplement for depression in people with obesity and low omega-3 levels

Tests an EPA omega-3 supplement against placebo for depression in adults with obesity.

Plain-language title generated from the registry record
Registry title: NUTRIMOOD-Inflammation and Depressive Comorbidity in Obesity: Modulation by Omega-3 Polyunsaturated Fatty Acids Status

Key facts

Where
Taichung, TaiwanSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 54 years old?

Source: NCT07439744, who can take part

Where in Taiwan

  • Mind-Body Interface Research Center (MBI Lab & Care)Taichung, TaiwanTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
National Science and Technology Council, Taiwan
Trial code
NCT07439744
Record updated
27 February 2026
Original description
A 12-week, randomized, placebo-controlled trial testing the efficacy of n-3 PUFA treatment (EPA, 2 g/day) in alleviating depressive symptoms in a subgroup of obese subjects with comorbid depression and low n-3 PUFA status (n-3 index < 8%) (81), from the Taiwanese cohort. Associations with PLA2/COX2 genotypes, lifestyle, nutritional profiles and gut microbiota will also be determined.Read full original descriptionShow less

Effects of 12-week n-3 PUFA Treatment (EPA) on Depressive Symptoms in Overweight/Obese Depressed Subjects With Low n-3 PUFA Status: Relationship With Systemic Inflammation

A 12-week, randomized, placebo-controlled trial testing the efficacy of n-3 PUFA treatment (EPA, 2 g/day) in alleviating depressive symptoms in a subgroup of obese subjects with comorbid depression and low n-3 PUFA status (n-3 index < 8%) (81), from the Taiwanese cohort. Associations with PLA2/COX2 genotypes, lifestyle, nutritional profiles and gut microbiota will also be determined.

Inclusion: Major depressive disorder; Antidepressant drug-free.

Exclusion: Alcohol or drug abuse/dependence (except for nicotine); Anxiety disorders (except for social phobia and generalized anxiety that are often comorbid with MDD); Obsessive-compulsive disorder; Post-traumatic stress disorder; Serious medical/neurological conditions, especially requiring corticosteroid/non-steroidal anti-inflammatory or immunosuppressive therapies or chronic thyroid hormone replacement; Schizophrenia; Mania; Active suicidal ideation.

ClinicalTrials.gov NCT07439744