Researchers conducted a 12-week, double-blind, randomized, placebo-controlled trial to assess the effectiveness of EPA or SPM treatments versus a placebo in managing Long COVID symptoms in adult patients. Researchers planned to enroll 240 eligible participants from various general and psychiatric hospitals in Taiwan. The focus was on evaluating the therapeutic impact and potential side effects of administering 3 g/day of EPA or 1.67 mg/day of SPMs on symptoms of depression in these patients. This consolidated approach aims to provide comprehensive insights into the efficacy of EPA and SPM treatments in Long COVID cases, addressing crucial mental health aspects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
54
A total daily dose of 3 g, administered as six capsules
A total daily dose of 1.67 g, administered as six capsules
Six capsules containing soybean oil daily
Mind-Body Interface Research Center (MBI Lab & Care)
Taichung, Taichung, Taiwan
Hamilton Depression Rating Scale (HAMD)
Adult depressive symptoms were assessed using the 21-item HAMD at baseline (week 0) and at weeks 1, 2, 4, 8, and 12.
Time frame: (week 0) and at weeks 1, 2, 4, 8, and 12
Erythrocyte Omega-3 Polyunsaturated Fatty Acids
Peripheral blood samples were collected at baseline and at the end of the 12-week intervention period using EDTA-containing tubes for erythrocyte fatty acid analysis
Time frame: Week 0 and Week 12
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