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Clinical Decision Support System for Depression (AID-ME Trial)
AID-ME Trial Summary
This trial will test a new digital health platform to help doctors treat patients with depression. The goal is to see if it improves patient outcomes.
- Depression
AID-ME Trial Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.AID-ME Trial Design
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Who is running the clinical trial?
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- Group 1: Active Intervention
- Group 2: Active Control
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
How many healthcare facilities are currently involved in the implementation of this trial?
"This trial is conducted in Douglas Mental health University Institute (Verdun, Quebec), GMF Centre Médical Métro Monk (Montréal, Ontario), McGill University Health Care Centre (MUHC) in Toronto, Vermont and 16 other medical institutions."
How many individuals are being observed in this clinical trial?
"Affirmative. The clinicaltrials.gov website reflects that this trial, which was inaugurated on June 16th 2022 is currently recruiting participants. In total, the study requires 500 people from 16 locations to take part in the research."
Are recruitment efforts for this experiment ongoing?
"Affirmative. Clinicaltrials.gov displays that this research is presently enrolling patients; the trial was first made available on June 16th 2022, and last modified on September 26th 2022. The study requires 500 participants between 16 different sites to complete it"
Who else is applying?
What state do they live in?
How old are they?
What site did they apply to?
What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
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