Indicated Prevention With Omega-3 Fatty Acids in Adolescents With 'At-Risk-Mental-State' for Psychosis
Launched by MEDICAL UNIVERSITY OF VIENNA · Nov 6, 2006
Trial Information
Current as of May 18, 2025
Completed
Keywords
ClinConnect Summary
1. Aims of the study The principal aim is to test if 1.2 g/day EPA/DHA can prevent transition to first-episode psychosis in 13-25 year old ultra-high risk individuals.
Specifically we propose to investigate:
* The clinical effects of EPA/DHA supplementation as an adjunct to standard therapy in individuals with 'At-Risk Mental State' (ARMS) for psychosis as defined by the PACE criteria (Yung et al., 1998).
* Lipid metabolism in peripheral tissue pre/post treatment by 1./analyzing bioactive lipid composition of red-blood cell membranes, 2./measuring phospholipase A2 (cPLA2) activity...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. /written informed consent (for individuals under 18 written informed consent of at least one of the parents is required),
- • 2. /age between 13 and 25 years,
- • 3. /ARMS as classified by the PACE criteria (Yung et al., 1998)
- PACE criteria for ARMS include one or more of following characteristics which must have occurred within the last 12 months:
- • Frank psychotic symptoms \< 1 week (Transient psychosis group)
- • Attenuated psychotic symptoms \> 1 week, \> 2 times per week
- • Decline in global function (drop in GAF of \> 30%) plus family history of psychosis or individual has schizotypal personality disorder To operationalize PACE criteria duration and severity ratings of psychotic symptoms will be performed using the Positive and Negative Syndromes of Schizophrenia Scale (PANSS) (Kay et al., 1987) applying following cut-off scores, following Morrison et al (2002): Ad 1) Transient psychosis is defined with the presence of symptoms that score 4 or more on hallucinations, 4 or more on delusions, or 5 or more on conceptual disorganizations, last less than one week and resolve without antipsychotic medication. Ad 2) Attenuated psychotic symptoms are defined by the presence of symptoms that score 3 on delusions, 2-3 on hallucinations, 3-4 on suspiciousness or 3-4 on conceptual disorganization.
- Exclusion Criteria:
- • 1. /Acute suicidal behaviour, aggressive behaviour (PANSS hostility, suicidality = 7),
- • 2. /Drug abuse that contributed decisively to the presentation of the index episode, (dependency on morphine, cocaine, amphetamine, but not THC),
- • 3. /Alcohol abuse if considered as major problem,
- • 4. /Epilepsy,
- • 5. /Mental Retardation (IQ\<80),
- • 6. /Pregnancy and lactation,
- • 7. /Structural changes in MRI or CT scan (e.g., tumours), expect for enlargement of ventricles or sulci,
- • 8. /Previous history of antipsychotic drug (\>1 week) or mood stabilizer treatment,
- • 9. /Laboratory values more than 10% outside the normal range for transaminases, CRP or bleeding parameters,
- • 10. /Individuals with organic brain syndrome,
- • 11. /Individuals who are taking anticoagulants,
- • 12. /Individuals who are taking omega 3 supplements, currently or within 8 weeks of being included in the trial,
- • 13. /Individuals who have other, severe, intercurrent illness which in the opinion of the investigator may put them at risk or influence the results of the trial or affect ability to take part in the trial.
About Medical University Of Vienna
The Medical University of Vienna is a leading research institution dedicated to advancing healthcare through innovative clinical research and education. Renowned for its commitment to excellence in medical science, the university fosters interdisciplinary collaboration among researchers, clinicians, and academic professionals. Its clinical trials encompass a wide range of medical disciplines, aiming to develop cutting-edge therapies and improve patient outcomes. With state-of-the-art facilities and a strong emphasis on ethical standards, the Medical University of Vienna is at the forefront of transforming scientific discoveries into practical applications that enhance global health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Vienna, , Austria
Patients applied
Trial Officials
G Paul Amminger, MD
Principal Investigator
Medical University of Vienna
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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