Omega-3 fatty acids
Fish-oil fats tested to prevent psychosis in young people at high risk. The first trial was strongly positive; three larger trials were not.
At a glance
- Type
- Medicine: dietary supplement
- Used for
- Tested to prevent psychosis in young people at high risk
- Status
- In trials
- Evidence
- EarlyHow evidence is rated
- Administration
- Capsules, daily. In the trials, for 3 to 6 months
- In Europe
- Tested in Austria and, in the PURPOSE trial, in 8 European countries. Part of the PsyCARE trial in France
Clinical summaryFor health professionals
- Vienna (Amminger 2010): 81 people aged 13 to 25 at ultra-high risk, 1.2 g a day for 12 weeks; psychosis by 12 months in 2 of 41 against 11 of 40 on placebo. At a median of 6.7 years: 4 of 41 against 16 of 40 (Amminger 2015).
- NEURAPRO (McGorry 2017): 304 people at 10 sites, 1.4 g a day for 6 months with case management; psychosis by 12 months in 11.5% against 11.2%. No difference at 3.4 years (Nelson 2018).
- PURPOSE (Winter-van Rossum 2025): 135 people aged 13 to 20 in 8 European countries and Israel, 6 months; psychosis in 5 of 67 against 3 of 68; stopped early.
- Meta-analysis of 24 trials, 3,236 people at clinical high risk: no intervention, omega-3 included, had a robust effect on transition (Minichino 2025).
What they are
Omega-3 fatty acids, found in fish oil, are long-chain fats built into the membranes of brain cells. They also dampen inflammation.1 They were tested in young people at high risk of psychosis, who have mild or brief psychotic symptoms but not a full psychotic illness, to see whether they could prevent one.
How well they work
The first trial, in Vienna, was strikingly positive. Of 81 young people at high risk, those who took omega-3 for 12 weeks developed psychosis far less often within a year: 2 of 41, against 11 of 40 on placebo.1 After almost seven years, the difference held: 4 of 41 against 16 of 40.2
Larger trials did not confirm it. In NEURAPRO, at 10 sites in Australia, Asia and Europe, 304 young people took omega-3 or a placebo for six months, alongside regular support from a case manager. After a year, about 11 in 100 in each group had developed psychosis.3 After three and a half years, there was still no difference.4
The European PURPOSE trial, led from Utrecht, included 135 young people aged 13 to 20 in eight European countries and Israel. Psychosis developed in 5 of 67 on omega-3 and 3 of 68 on placebo; the trial stopped early, mainly because the COVID-19 pandemic slowed recruitment.5 Across 24 trials with 3,236 people at high risk, no preventive treatment, omega-3 included, reliably lowered the number who went on to develop psychosis.6
Side effects
In the trials, side effects were no more common on omega-3 than on placebo.1,5
Trials in Europe
The PsyCARE trial in France assigns omega-3 or N-acetylcysteine (opens in a new tab) to people with psychosis according to their biological profile.7
What we don’t know yet
- Why the Vienna trial found such a large effect and the larger trials none.
- Whether omega-3 helps a subgroup, for example people with low levels of these fats in their blood.
