CompletedPhase 4ACTRN12614000390684

Fish oil in chronic psychiatric outpatients with anxiety and mood disorders.

Adjunctive natural low dose docosahexaenoic acid (DHA) omega-3 in a 16 week random double-blind placebo controlled (RDBPC) cross-over withdrawal study in a group of chronic, psychiatric out-patients with anxiety and mood disorders.


Sponsor

Dr Michael Piperoglou

Enrollment

60 participants

Start Date

May 1, 2014

Study Type

Interventional

Conditions

Summary

To investigate the effectiveness of the adjunctive role of DHA omega-3 in outpatients with chronic anxiety and depression.


Eligibility

Sex: Both males and femalesMin Age: 20 YearssMax Age: 70 Yearss

Inclusion Criteria2

  • Outpatients with chronic anxiety and/or depressive symptoms.
  • Patients currently taking DHA (NeuroSpark) capsules for at least 3 months prior to study entry.

Exclusion Criteria8

  • ADHD
  • Brain injury
  • Mild cognitive impairment
  • Dementias
  • Substance dependence and/or abuse
  • Schizophrenia
  • Acutely suicidal patients
  • Chronic unstable medical conditions

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Interventions

Natural low dose docosahexaenoic acid (DHA) omega-3 (NeuroSpark) 130-390mg per day in addition to standard psychiatric treatments. The dose in the study is the dose which has been found clinically

Natural low dose docosahexaenoic acid (DHA) omega-3 (NeuroSpark) 130-390mg per day in addition to standard psychiatric treatments. The dose in the study is the dose which has been found clinically to be appropriate and efficacious for each individual entering the study. Oral. This study medication will be administered for 16 weeks (24 week study minus 8 weeks on placebo = 16 weeks of study medication). There is no washout period. Adherence to study medication regimen will be monitored via capsule return and self-report daily diary entries.


Locations(1)

VIC, Australia

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ACTRN12614000390684