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Clinical Trials in Canada / NCT07725289
Starting soon Not applicable

Clinician Practice Companion to Address Youth Substance Use

NCT07725289 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2027-01
Last updated
2026-09-23

Condition(s) studied

Substance UseSubstance-Related DisordersAdolescent Substance UseCannabis UseOpioid Use DisorderDrug OverdoseOverdose PreventionCo-occurring Mental Health Conditions

Investigational drug(s) / intervention(s)

Practice Companion

Practice Companion: A written, multi-strategy practice companion that guides clinicians and other trusted adults in acute and community settings to deliver developmentally appropriate substance use care to youth. Content is organized by substance and by pattern of use. It includes scripts for initiating non-stigmatizing conversations and guidance and referrals for connecting youth and families to care, spanning cannabis and other substance use, overdose prevention as a core component (naloxone, take-home drug testing strips, harm reduction education, and medications for opioid use disorder), and co-occurring mental health needs. The practice companion is youth- and family-centered and attends to how gender, sexuality, poverty, and housing instability intersect with substance use. Site-specific adaptations are provided for the British Columbia, Québec, and Massachusetts settings.

Study summary

Substance use, including the use of opioids, cannabis, and other drugs, is common among adolescents and young adults, and overdose has become a leading cause of death among youth in Canada and the United States. Many young people who use substances also experience co-occurring mental health concerns. Evidence-based approaches to youth substance use care exist, including harm reduction, overdose prevention (such as naloxone and take-home drug testing strips), and medications for addiction treatment. These approaches remain adult-oriented, however, unevenly implemented in youth-serving settings, and insufficiently centered on the needs and goals of youth and their families.

This study develops and pilot tests a written "practice companion" that helps clinicians and other trusted adults provide developmentally appropriate substance use care to youth ages 14 to 24 in hospital and community settings. The practice companion offers practical, easy-to-use guidance organized by substance and by pattern of use. It addresses cannabis and other substances that youth commonly use and that clinicians frequently seek support with, alongside a strong focus on overdose prevention through its core elements: naloxone, take-home drug testing strips, harm reduction education, and medications for opioid use disorder. It also attends to co-occurring mental health needs and to how gender, sexuality, housing instability, and other social and structural contexts shape substance use and care.

The research team will first interview youth who use substances, their families and caregivers, and clinicians to learn how each element of care should be adapted for young people. The team will then produce the practice companion and pilot test it with 60 youth across three sites, in British Columbia, Québec, and Massachusetts. After receiving care guided by the practice companion, youth will complete an interview about whether the care was relevant, useful, appropriate, and acceptable. Families and clinicians will also be interviewed to assess how feasible, sustainable, and faithful to its design the practice companion is in practice.

Throughout the study, the team will work closely with youth and families who have lived experience through a community-based participatory research approach that includes Community Advisory Boards. The work centers equity for Black, Indigenous, and other racialized youth, Two-Spirit and LGBTQ+ youth, and youth experiencing housing instability. Findings will guide a larger future study of the practice companion's effectiveness.

Eligibility

Sex
ALL
Min age
14 Years
Max age
24 Years
Healthy volunteers
Accepted
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.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Adolescent and Young Adult Medicine, Mass General Brigham for Children Boston Massachusetts
BC Children's Hospital Vancouver British Columbia
Foundry (Foundry Central Office) Vancouver British Columbia
Centre de Recherche du CHUM (CRCHUM) Montreal Quebec
CHU Sainte-Justine Montreal Quebec

More Massachusetts General Hospital trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07725289 on ClinicalTrials.gov ↗ ← All trials in Canada