Can a simple guide help clinicians better address youth substance use?
NCT ID NCT07725289
First seen Jul 24, 2026 · Last updated Sep 09, 2026 · Updated 3 times
Summary
This study develops and pilot tests a written 'practice companion' designed to help clinicians and other trusted adults provide developmentally appropriate substance use care to youth ages 14 to 24. The companion offers practical guidance on cannabis, opioids, and other substances, with a focus on overdose prevention and harm reduction. Researchers will interview youth, families, and clinicians to assess whether the care is acceptable, useful, and feasible in hospital and community settings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a written practice companion guiding clinicians in youth substance use care
- What this could lead to
- If successful, this practice companion could offer a practical tool to improve substance use care for adolescents and young adults, potentially reducing overdose risk.
- What could go wrong
- This is a small pilot study with only 60 participants, so results may not generalize. The intervention is behavioral and depends on clinician uptake, which may vary.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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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.
- Ages
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14 to 24 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Ages 14 to 24 years. * Uses drugs or alcohol (past year). * Receiving care at a participating study site. Exclusion Criteria: * Cognitive limitations or intellectual disabilities that prevent provision of informed consent. * Any medical or psychiatric condition causing acute distress or requiring emergency evaluation. * Current membership on a study Community Advisory Board.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
5 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
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Locations
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Adolescent and Young Adult Medicine, Mass General Brigham for Children
Boston, Massachusetts, 02114, United States
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BC Children's Hospital
Vancouver, British Columbia, V6H 3N1, Canada
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CHU Sainte-Justine
Montreal, Quebec, H3T 1C5, Canada
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Centre de Recherche du CHUM (CRCHUM)
Montreal, Quebec, H2X 0A9, Canada
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Foundry (Foundry Central Office)
Vancouver, British Columbia, Canada
Contact Email: •••••@•••••
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