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:
- You have some symptoms of depression, measured by a standard questionnaire score of 5 or higher (PHQ-8)
- Your memory and thinking abilities are within a healthy range, based on a standard cognitive test score of 20 or higher (MoCA)
- You are able and willing to sign a consent form and agree to take part in the study
- You feel comfortable using a tablet computer based on your own assessment of your tech skills
- You have sufficient vision and hearing — with the help of glasses, hearing aids, or other assistive devices if needed — to use a tablet and take part in a small group of about 6 people
- You can fluently read, speak, and understand either Hebrew or English
Who may not be able to join:
- You have been diagnosed with a condition that affects brain function or causes it to decline over time, such as Mild Cognitive Impairment, dementia, or Parkinson's disease (based on what you report about yourself)
- You have been diagnosed with certain mental health conditions other than depression or anxiety — specifically schizophrenia, bipolar disorder, or psychotic disorders (based on what you report about yourself)
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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Adaptive Cognitive Evaluation (ACE) Battery; Canadian Occupational Performance Measure (COPM)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.