Fish oil and Body's own healing molecules could lift long COVID depression
NCT ID NCT07711444
First seen Jul 17, 2026 · Last updated Jul 22, 2026 · Updated 2 times
Summary
This study tests whether two dietary supplements—eicosapentaenoic acid (EPA), an omega-3 fatty acid, and specialized pro-resolving lipid mediators (SPMs)—can reduce depressive symptoms in adults with long COVID. Participants take either EPA, SPMs, or a placebo daily for 12 weeks. The goal is to see if these natural compounds can improve mood and mental health after a COVID-19 infection.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Eicosapentaenoic acid (omega-3 fatty acid) and Specialized Pro-Resolving Lipid Mediator (SPM)
- What this could lead to
- If effective, these supplements could offer a new, low-risk way to treat depression in long COVID patients.
- What could go wrong
- This is a small, early-stage trial, and results may not apply to everyone. Supplements can have side effects and may not outperform placebo.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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54 people
The number who actually took part.
- Started
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Jun 2024
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Confirmed SARS-CoV-2 infection by PCR, documented positive test, or clinician diagnosis * Meeting CDC criteria for Post-COVID Conditions (Long COVID) as the presence of new, returning, or ongoing symptoms ≥4 weeks after confirmed SARS-CoV-2 infection * Hamilton Depression Rating Scale (HAMD-21) score ≥18 at baseline * Stable antidepressant treatment for ≥4 weeks or no current antidepressant use; and * Ability to provide written informed consent Exclusion Criteria: * Current or past six-month diagnosis of psychotic disorder, bipolar disorder, substance use disorder, or other major psychiatric conditions based on ICD-10 or DSM-5 criteria * Significant neurological or medical comorbidities (eg, epilepsy, traumatic brain injury, autoimmune disease, cancer), acute infections, or clinically significant laboratory abnormalities * Regular use of SPM or EPA supplementation \>0·5 g/day * Known allergy or intolerance to omega-3 fatty acids or SPMs; and * Requirement for inpatient psychiatric care due to acute suicide risk
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Mind-Body Interface Research Center (MBI Lab & Care)
Taichung, Taichung, 404, Taiwan
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