Depression and Anxiety Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 19 or older who have been diagnosed with unipolar depression (a form of depression without manic episodes) by a licensed doctor, based on recognised international diagnostic standards
- People who are willing and able to take part in data collection as required by the study
- People who are willing to sign consent forms and allow their relevant information to be shared before the study begins
- People who are willing to allow their data to be used for research and publication by the Sha Research Foundation, in line with privacy laws
- People who are willing to practise daily mindfulness exercises for at least 30 minutes each day and follow the study's guidelines
Who may not be able to join:
- People who do not meet the inclusion criteria listed above
- People who have been diagnosed with bipolar disorder or schizophrenia (a condition involving psychosis or breaks from reality)
- People who are currently being treated with a strong type of antipsychotic medication known as highly potent neuroleptics
- People who are unwilling to take part in data collection
- People who are unable to commit to the daily mindfulness practice of at least 30 minutes
- People who are currently pregnant or breastfeeding; if a participant becomes pregnant during the study, their participation would need to end
- People with serious mental health conditions, such as schizophrenia
There are no exclusions based on national origin, culture, ethnicity, race, sex, physical disability, sexual orientation, religion, or spiritual practices.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Peter Hudoba De Badyn, MD, FRCS,, Sha Research Foundation
Phone: 604-904-7712
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Mean Change from Baseline in Quality of Life Scores on 36-item short-form Quality of Life Questionnaire (SF-36) at 6 weeks; Mean Change from Baseline in Scores on PHQ-9 questionnaire at 6 weeks; Mean Change from Baseline in Scores on BAI-21 (Beck Anxiety Inventory) Scale at 6 weeks
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.