22q11 Deletion Syndrome Clinical Trial
Official title:
Indicated Prevention With Long-chain Polyunsaturated Omega-3 Fatty Acids in Patients With 22q11 Microdeletion Syndrome Genetically at High Risk for Psychosis: A Randomised, Double Blind, Placebo-controlled Treatment Trial.
The purpose of the present trial is to investigate the effects of omega-3 PUFAs in individuals aged 12-26 years with 22q11DS at ultra-high risk for developing a first episode of psychosis.
We will use a prospective, randomized, double-blind, placebo-controlled, single-centre study
design. Eighty individuals aged 12-26 will be randomly assigned in two treatment conditions
(40 in each arm) at the Department of Neuroscience, Children Hospital Bambino Gesù, Rome,
Italy. Randomisation will be arranged by the Clinical Trials Department of the same
hospital. Participants will receive 4 capsules (2 in the morning; 2 in the evening) for a
period of 12 weeks. The active treatment is a supplement of yellow gelatine 0.625 g capsules
containing concentrated marine fish oil. The daily dose of 4 capsules will provide
approximately 700 mg of eicosapentaenoic acid (EPA, 20:5n3), 480 mg of docosahexaenoic acid
(DHA, 22:6n3), and 7.6 mg of Vitamin E. Vitamin E is added as an antioxidant to fish oil
capsules to stabilize highly unsaturated fatty acids. Participants will receive either 4
capsules of 0.7g marine fish oil or 4 capsules of 0.7g of paraffin oil (which is not
absorbed by the gastrointestinal tract) per day. The daily dose of omega-3 PUFAs is based on
our previous trail (Amminger et al., 2010).
All patients will receive standard treatment, which includes management by a psychiatrist or
resident psychiatrist and non-neuroleptic pharmacotherapy as clinically indicated.
Specifically, Cognitive-behavioural therapy (CBT) embedded within case management will be
administered. The CBT will be based on the models developed at the PACE Clinic in Melbourne,
in the EDIE trial, and in Cologne, as these have proven to be effective in RCTs. The number
of sessions delivered will be captured for each client. In addition, fidelity will be
monitored by therapists rating their own sessions on an established checklist of therapeutic
interventions. Any additional psychosocial interventions delivered will also be documented.
The case management component will consist of therapists addressing current interpersonal
and social issues and providing practical help. 6 - 20 CBCM sessions will be provided within
the first 6 months.
Hypotheses:
1. Omega-3 PUFAs have a positive effect on clinical course and outcome in UHR+22q11DS
individuals
Specifically that at 12 months follow-up:
- The transition to psychosis rate is significantly lower in the omega-3 PUFA group
- Ratings on CAARMS, PANSS, MADRS, GAF improve significantly more in the omega-3
PUFA group
- Neuropsychological functioning is significantly better in the omega-3 PUFA group.
2. Lipid metabolism characteristics described in schizophrenia will be more prevalent in
individuals who make transition to psychosis
- Reduced omega-3 PUFAs and reduced nervonic acid (Amminger et al., 2011) and
increased PLA2 activity at baseline characterize individuals who develop psychosis
- PLA2 activity will significantly decrease pre/post treatment in the omega-3 PUFA
group
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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