Please note: This trial has finished recruiting and is not accepting new participants.

Research Center: The Melbourne Clinic
Location: Richmond, Melbourne
Lead Doctor: Dr Jerome Sarris
Ethics Committee: Reviewed and approved by Melbourne Clinic Research Ethics Committee (project number 220)

Background

Approximately 1 in 7 Australians will experience depression in their lifetime. Unfortunately, antidepressants are not always successful in completely addressing symptoms.

This study is investigating whether a special combination of natural supplements, taken together with antidepressants,  can relieve symptoms in people with depression. Examples of these supplements include Omega 3, Zinc and Folic Acid, which are safe to consume and have been available as supplements for many years.

This study seeks men and women who are experiencing symptoms of depression and currently taking antidepressants. Participants are required to attend 4 study visits every 2 weeks over a 2 month period. Participants will be reimbursed $100 for their time and expenses and provided with a 2 month supply of the study supplement at the completion of the trial.

Benefits of Participation

• You may experience improvements in your depression symptoms.
• You will be provided with a 2 month supply of a few select study supplements (at the completion of the trial), at no charge.
• Your psychological condition will be carefully monitored by health professionals.
• You will be compensated $100 to cover your travelling expenses.
• You will be helping to advance medical research.

Your Rights

• If you decide to participate in the study and later feel that you no longer wish to be part of it, you may withdraw at any time.
• Your records relating to this study and any other information received will be kept strictly confidential.
• Qualified health professionals will monitor your health as it relates to the study.

Who Can Participate?

• Men and women aged 18 to 75 who are currently experiencing symptoms of depression
• Are currently taking antidepressants and have been for the past 4 weeks
• Willing to attend the 4 study visits every 2 weeks at the research site over a 8 week  period.