Why are BIPOC patients less likely to stick with antidepressants? new study investigates
NCT ID NCT06799078
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study explores why Black, Indigenous, and People of Color (BIPOC) may have lower rates of starting and sticking with antidepressants after a one-time psychiatric consultation. Researchers will survey 60 adults diagnosed with depression to see if race affects whether they get recommended medication, start it, take the right dose, and stay on it. The goal is to understand barriers to fair treatment and inform better care strategies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could point toward ways to reduce racial disparities in depression treatment, leading to more equitable care for BIPOC communities.
- What could go wrong
- This is an observational study with only 60 participants, so findings may not apply broadly. It does not test a new treatment, so direct patient benefits are limited.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Mar 2024
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients who received an outpatient psychiatric consultation at CAMH within the past 3 months and received a diagnosis of depression, after which they were discharged to the care of their primary care provider
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Able and willing to sign and date the informed consent form 2. Stated willingness to comply with all study procedures 3. Age 18 years and older 4. Diagnosis of depression in a psychiatric consultation at CAMH in the last 3 months 5. Not currently followed by a psychiatrist 6. Able to complete the REDCap questionnaire in English using the internet Exclusion Criteria: 1. Presence of a life-time diagnosis of bipolar disorder or schizophrenia 2. Potential participants with a suicidal plan or intent whose consulting psychiatrist determined are in need of immediate clinical attention (e.g., referral to CAMH ED, voluntary or involuntary hospitalization) 3. Acute psychosis (e.g., MDD with psychotic features)
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Depression - major depressive disorder are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Centre for Addiction and Mental Health
Toronto, Ontario, M5S 2S1, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can brain stimulation rewire how depressed patients learn from rewards?
- Can a personalized mix of nerve stimulation and therapy rewire the brain for better mental health?
- Can lay workers in uganda talk depression down?
- Can a computer model outsmart depression in older adults?
- Heartbeat vibrations: a new way to ease anxiety and depression?
- Can a single shot of ketamine calm suicidal distress in the ER?