Substance Use

64

Review clinical trials related to Substance Use. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Mobile Technology to Reduce Teen Substance Misuse

The goal of this study is to test the newly expanded WisePath for Teens (WPT) for substance use app, a direct-to-consumer paired mobile phone app for iOS and Android platforms that supports parents/guardians in delivering evidence-based techniques to reduce youth substance abuse and co-occurring mental health problems. This project will expand WPT for use with a general population of teens with problematic substance use and their parents to reduce substance abuse, its harmful effects, opioid overdoses, and progression to substance use disorders, as well as other behavioral health problems that are exacerbated by substance abuse and/or interfere with substance abuse treatment.

Participants needed: 600
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: Evidence-Based Practice Institute, Seattle, WAUpdated: Aug 20, 2026Locations: 2
Eligibility criteria

Resides in United States [+15]

Participated in previous iKinnect or WisePath for Teens research in the past 2 y... [+2]

Status: Recruiting

Linking Individuals Needing Care for Substance Use Disorders to Peer Coaches & Across INcarceration Settings

The goal of this study is to learn whether a virtual peer recovery coach (PRC) intervention can improve engagement in addiction treatment among incarcerated adults with substance use disorders. The main questions it aims to answer are: * Does the PRC intervention increase engagement with at least one recovery resource at 30 and 90 days? * Does it improve secondary outcomes such as substance use, recovery capital, overdose events, and recidivism? Researchers will compare Treatment-as-Usual with the PRC telehealth intervention to see if PRC support improves engagement in addiction care. Participants will: * Complete baseline and follow-up assessments * Receive either Treatment-as-Usual or a virtual PRC session focused on motivational interviewing and linkage to recovery resources

Participants needed: 550
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Emory UniversityUpdated: Aug 17, 2026Locations: 3
Eligibility criteria

Incarcerated at participating jail [+4]

Cognitive impairment (inability to comprehend the informed consent document as a... [+2]

Status: Recruiting

CARS: Cannabis and Alcohol Reduction Study

The study will test a computerized treatment with subjects ages 13-17 years who are seeking treatment for alcohol and/or cannabis use. Follow-up assessments will be conducted at one- and three-months following treatment.

Participants needed: 52
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: Medical University of South CarolinaUpdated: Aug 13, 2026Locations: 1
Eligibility criteria

between the ages of 13 and 17 [+3]

Status: Recruiting

Testing and Evaluation of the Returning to the Land Intervention to Address and Prevent Substance Misuse

This study aims to test the Returning to the Land intervention in partnership with a tribal community. The program is designed to address caregiver substance use and child emotional and behavioral development.

Participants needed: 60
Trial details
Age: 14-19Biological sex: AllType: InterventionalSponsor: Johns Hopkins Bloomberg School of Public HealthUpdated: Aug 5, 2026Locations: 1
Eligibility criteria

Reside on or near the Rocky Boy Reservation (~50-mile round trip); [+2]

Any condition preventing meaningful participation (e.g., lacking capacity to con...

Status: Recruiting

iPAWS: Improving Pain Management After Wisdom Tooth Extraction Surgery

This is a clinical trial that will evaluate the feasibility and acceptability of a virtual brief program for adolescents and young adults undergoing wisdom tooth extraction and their parents. The program aims to teach youth safe and effective ways to manage post-surgical pain as well as decrease risky health behaviors.

Participants needed: 150
Trial details
Age: 15-20Biological sex: AllType: InterventionalSponsor: Brown UniversityUpdated: Jul 28, 2026Locations: 1
Eligibility criteria

Ages 15 to 20 years [+4]

Status: Not yet recruiting

Clinician Practice Companion to Address Youth Substance Use

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.

Participants needed: 60
Trial details
Age: 14-24Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Jul 27, 2026Locations: 5
Eligibility criteria

Ages 14 to 24 years. [+2]

Cognitive limitations or intellectual disabilities that prevent provision of inf... [+2]

Status: Recruiting

Cultural Adaptation of Drug Treatment for DJJ Youth

This project aims to improve the understanding of the impact of Ethnic and Racial Discrimination (ERD) on adolescent alcohol and other drug use (AOD) within the Black Justice-Involved Youth (JIY) population. Individual interviews with Black JIY and focus groups with parents and guardians of Black JIY and community members who support change and reform in the justice community for Black JIY will be conducted.

Participants needed: 55
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Jul 13, 2026Locations: 2
Eligibility criteria

A guardian of JIY [+9]

Status: Not yet recruiting

CBITS-RTM Pilot Study

This pilot study, conducted in partnership with juvenile detention centers, evaluates an adapted CBITS-RTM intervention delivered in a detention school setting.

Participants needed: 28
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Jul 6, 2026Locations: 1
Eligibility criteria

Youth must 1) be currently incarcerated in a partnering juvenile detention cente... [+1]

Observable cognitive or developmental delays or active psychosis that would inte...

Status: Recruiting

Feasibility of Incorporating a Standardized Substance Use Measure With Linked-Brief Intervention Into Routine Psychosocial Care of Adult Childhood Cancer Survivors

The ASSIST Study is designed to explore whether a brief, evidence based substance use screening and counseling approach can be easily integrated into routine survivorship care at St. Jude Children's Research Hospital. During a regularly scheduled psychosocial visit, participants complete the World Health Organization's Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST). This short questionnaire helps identify patterns of use related to tobacco, alcohol, cannabis, prescription medications, and other substances. Survivors whose results show possible risk receive a brief, supportive counseling session during the same appointment. This session uses motivational interviewing techniques to help individuals reflect on their use and consider steps to reduce potential harm. Primary Objective: \- Assess the feasibility and acceptability of integrating a standardized substance use screening and brief intervention protocol into routine psychosocial workflows within a survivorship clinic. Secondary Objective: \- Evaluate the fidelity of delivering a brief substance use intervention to reduce substance use behaviors among survivors.

Participants needed: 30
Trial details
Age: 15+Biological sex: AllType: InterventionalSponsor: St. Jude Children's Research HospitalUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Followed in the ACT Clinic at St. Jude Children's Research Hospital [+2]

Significant mental or cognitive impairment that would impact ability to complete...

Status: Not yet recruiting

Substance Use Prevention for Recently Displaced Adults - SUPRA (R33) RCT

This study is a randomized controlled trial among 144 internally displaced people to determine the feasibility, acceptability, and preliminary effectiveness of a single-session Acceptance of Commitment Therapy (ACT) group therapy on preventing or reducing substance use behaviors.

Participants needed: 144
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Boston Medical CenterUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Age 18 or over [+3]

Self-reported diagnosis of a substance use disorder [+1]

Status: Recruiting

Neuroimaging of Adolescent Cannabis Use Treatment

This study is testing whether brain activity related to learning can help predict how well teens respond to a treatment program designed to reduce cannabis use. Teens ages 14-17 will complete a brain scan and then take part in 10 weekly virtual sessions where they report cannabis use and complete drug tests at home. Participants can earn prizes for staying cannabis-free.

Participants needed: 80
Trial details
Age: 14-17Biological sex: AllType: InterventionalSponsor: Indiana UniversityUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

14-17 year old youth [+3]

Youth has a history of Fetal Alcohol Spectrum Disorder, intellectual disorders,... [+3]

Status: Recruiting

Finding Emotional Empowerment and Lifelong Strength

This study will build a partnership with a Community Advisory Board to co-produce, and then pilot test, a theory-guided mental health literacy intervention focused on trauma and substance use. Participants will take part in educational group sessions for 12 weeks and complete assessments at baseline and two follow-up time points (mid-intervention and post-intervention). Intervention participants will be randomly invited to post-study focus groups to gather feedback on their experiences in the program.

Participants needed: 80
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Self-identify as Black or African American [+4]

Status: Not yet recruiting

Development of a Mobile Health Intervention to Support Functioning of Veterans With Substance Use Disorders

This project will involve the development, refinement, and preliminary testing of a mobile health intervention (Motivational Enhancement Therapy Skills for Veterans; "METS4Vets"), which will be delivered through a smartphone app. The intervention will aim to support Veterans who are navigating the critical transition from structured residential substance use treatment to outpatient settings.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: VA Office of Research and DevelopmentUpdated: Jun 12, 2026Locations: 1
Eligibility criteria

current SUD diagnosis according to chart review [+3]

current psychosis [+3]

Status: Recruiting

Neurobehavioral Signatures of Sign- and Goal-Tracking in Emerging Adults: Translation of a Preclinical Model

This study seeks to understand individual differences in personality, brain function, and behavior. Study hypothesis: \- A stronger sign-tracking bias will be associated with a bottom-up processing style characterized by less adaptive attentional- and impulse-control as well as hyperactive reward processing, whereas a stronger goal-tracking bias will be associated with a top-down processing style characterized by strong attentional- and impulse-control as well as normative reward processing.

Participants needed: 294
Trial details
Age: 18-22Biological sex: AllType: InterventionalSponsor: University of MichiganUpdated: Jun 10, 2026Locations: 2
Eligibility criteria

18-22 years old at baseline [+4]

Acute or chronic medical or neurological illness (e.g., diabetes, epilepsy, migr... [+8]

Status: Recruiting

Adaptation and Evaluation of Bright Horizons

This study will test if a program called 'Bright Horizons' is effective at reducing binge substance use among adolescents. Bright Horizons is a culturally adapted intervention developed and tested through a partnership between The White Mountain Apache Tribe and Johns Hopkins University. Bright Horizons is a brief intervention that teaches emotion regulation, coping skills, and problem solving. The intervention also uses goal setting to reduce alcohol and other substance use and to connect to individuals with treatment.

Participants needed: 100
Trial details
Age: 10-24Biological sex: AllType: InterventionalSponsor: Johns Hopkins Bloomberg School of Public HealthUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Aged 10-24 [+4]

Unstable and severe medical, psychiatric or drug use problems that necessitates... [+4]

Status: Recruiting

The Development and Evaluation of a Culturally Grounded ENDS Intervention for Rural Hawaiian Youth

The purpose of this research proposal is to develop and evaluate a culturally grounded, ENDS prevention intervention for rural Hawaiian youth. This will be accomplished through two specific aims. AIM 1 (Years 1-3) are focused on pre-intervention and intervention development. In Year 1, youth focus groups will be conducted to assess the environmental demands related to ENDS use in rural Hawai'i. In Year 2, specific ENDS-related problem situations (i.e., situations that increase risk for ENDS use) will be extracted from the Year 1 focus groups and prioritized through survey methods with 200-250 predominately Native Hawaiian youth across 16 different middle/intermediate schools on Hawai'i Island. In Year 3, five situations found to be the most frequently experienced and/or difficult to manage by youth surveyed in Year 2 will serve as the foundation for the development of narrative scripts. Three of these scripts will be cast and filmed on location on Hawai'i Island by a professional film director, and will be edited into three short films, 6-8 video clips, and 6-8 professional photos or production stills. Similar to the investigators' prior drug prevention research in rural Hawai'i, classroom-based lessons will be created to support the short films. Additional lessons and videos from an evidence-based, culturally grounded substance abuse prevention curriculum for Hawaiian youth (Ho'ouna Pono) will be used to create a modular classroom curriculum. The video clips and professional photography/production stills will be embedded with prevention messaging, and will be used for a social and print media campaign to reinforce the classroom curriculum. AIM 2 (Years 4-5) is to evaluate the ENDS prevention intervention (classroom curriculum plus social/print media campaign) across all middle/intermediate public or public-charter schools (N = 16) and up to 11 different cultural immersion charter schools on Hawai'i Island using a dynamic wait-listed control group design.

Participants needed: 500
Trial details
Age: 10-14Biological sex: AllType: InterventionalSponsor: University of HawaiiUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

6th-8th grade students attending a public or public-charter school on Hawaii Isl...

K-5th grade students and 9th-12th grade students on Hawaii Island.

Status: Recruiting

Project REACH: A Comprehensive Telehealth Intervention at Syringe Service Programs to Engage People Who Use Drugs

This trial will assess the feasibility, acceptability, and preliminary effectiveness of Project REACH (Remote Engagement \& Access for Community Health), a telehealth intervention at syringe service programs (SSP) to improve access to HIV-related evidence-based interventions (EBI) for people who use drugs including those who inject them.

Participants needed: 121
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of MinnesotaUpdated: May 19, 2026Locations: 1
Eligibility criteria

18 years of age or older [+4]

Unable or unwilling to provide informed consent [+4]

Status: Recruiting

The Collaborative Care PrTNER Study

A randomized controlled trial to assess the ability of a Collaborative Care Prevention, Treatment, Navigation, Engagement, Resource (PrTNER) intervention to increase initiation of preexposure prophylaxis (PrEP) (for those at-risk for HIV) and decrease viral load (for those living with HIV) among young aged 15 to 29 through engagement in SU treatment.

Participants needed: 275
Trial details
Age: 15-29Biological sex: MaleType: InterventionalSponsor: Children's Hospital of PhiladelphiaUpdated: May 18, 2026Locations: 2
Eligibility criteria

15-24 years old; [+11]

Assigned female sex at birth [+9]

Status: Not yet recruiting

mHealth Service Linkage for Young Adults Impacted by the Criminal Legal System

This study is designed to test Project LYNX, a program designed to help young adults (ages 18-29) with recent criminal legal system involvement can find and get connected to substance use and HIV-prevention services in the community. The program combines support from a trained peer navigator with easy-to-use digital tools. The study will: * Adapt an existing navigator program by adding new digital (eHealth) tools that were co-developed with young adults. These tools will help navigators refer participants to the right health services. * Refine and test the updated program to make sure it works well and is easy to use. * Evaluate whether the program is feasible, acceptable, and helpful in linking young adults to substance use treatment and HIV-prevention services. The overall goal is to create a practical, user-friendly system that supports young adults find and get connected to services for substance use and HIV prevention that they need.

Participants needed: 50
Trial details
Age: 18-29Biological sex: AllType: InterventionalSponsor: University of PittsburghUpdated: May 20, 2026Locations: 1
Eligibility criteria

Self-report recent criminal legal involvement (past year); [+4]

Being on PrEP [+2]

Status: Recruiting

The Hastiin Bidziil (Strong Man) Intervention

The Hastiin Bidziil (Strong man) Intervention study is part of a larger project called, Community-Driven Indigenous Research, Cultural Strengths \& Leadership to Advance Equity in Substance Use Outcomes (CIRCLE) Center of Excellence. CIRCLE aims to address drug use related health problems in collaboration with diverse Indigenous communities. This study is a randomized controlled trial study to measure the effectiveness of a secondary prevention program, called Hastiin Bidziil (Strong Man), aimed at reducing substance use among Native American Indian (AI) men ages 18 years and older

Participants needed: 160
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: Johns Hopkins Bloomberg School of Public HealthUpdated: May 14, 2026Locations: 2
Eligibility criteria

Self-identify as American Indian [+4]

Any condition that would affect successful participation (e.g., planned move) [+2]

Status: Not yet recruiting

Permanent Supportive Housing Overdose Prevention+ Study

This community-partnered study examines a technical assistance intervention designed to help permanent supportive housing agencies implement evidence-based practices to prevent tenant overdose and improve tenant health.

Participants needed: 2,940
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: May 6, 2026Locations: 1
Eligibility criteria

Serve at least 40 tenants in New York and/or New Jersey [+4]

See inclusion criteria.

Status: Recruiting

Parenting in 2 Worlds Multisite Trial

This research study will test the effectiveness of a culturally grounded parenting intervention called Parenting in 2 Worlds (P2W). This intervention is designed for American Indian / Alaska Native (AI) parents/guardians of adolescents who reside in urban areas. This will be a multi-regional effectiveness trial across four regions: Northeast (Buffalo/Niagara), Midwest (St. Paul/Minneapolis), Mountain (Denver), and Southwest (Phoenix). There are four specific aims. First, this study will test the effectiveness of Parenting in Two Worlds (P2W) as compared to an informational family health intervention, Healthy Families in 2 Worlds (HF2W), in improving parenting and family functioning. Second, this study will test if the relative effectiveness of P2W, compared to HF2W, varies by parent's/guardian's level of socioeconomic vulnerability, experiences of historical loss, or AI cultural identity. Third, this study will examine if P2W can reduce adolescent (ages 12 - 17) risky health behaviors including substance use, depressive symptoms, suicidality, and risky sexual behaviors. Fourth, this study will examine whether positive changes in parenting and family functioning that result from P2W lead to positive changes in adolescent's health behaviors.

Participants needed: 1,440
Trial details
Phase: Phase 2Age: 12+Biological sex: AllType: InterventionalSponsor: Arizona State UniversityUpdated: Apr 29, 2026Locations: 4
Eligibility criteria

Must be American Indian parents or guardians of American Indian children aged 12... [+6]

Not applicable

Status: Recruiting

Women Focused Encounters for Resilience Independence Strength and Eudaimonia

The goal of this combination Type 1 hybrid and observational study is to evaluate the impact of a peer delivered intervention of acceptance and commitment therapy (ACT) + exercise + social support to address the substance (ab)use, violence, and AIDS/HIV (SAVA) to improve medication adherence for women living with HIV (WLWH). This intervention will be implemented by community based organizations that focus on WLWH across four counties. The main question it aims to answer are: * Will peer provision of ACT, exercise, and social support improve medication adherence for WLWH? * Will community based organizations be able to sustain the intervention after research is completed, and what changes will need to be made to sustain the intervention.

Participants needed: 300
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of California, San DiegoUpdated: May 1, 2026Locations: 1
Eligibility criteria

Is a woman [+7]

Unwilling to participate in video record sessions (used to evaluate the quality... [+2]

Status: Recruiting

Health Surveillance at Constructor University Bremen (CUB) and Among HAW-Hamburg Employees

The aim of Health Surveillance is to analyze and describe the state of health of students at Constructor University, key influencing factors and individual resources by using mixed-method design.

Participants needed: 363
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Jacobs University Bremen gGmbHUpdated: May 1, 2026Locations: 2
Eligibility criteria

English language skills [+4]

Illiteracy [+1]

Status: Not yet recruiting

Mindfulness-Based Substance Use Prevention (MINDS-UP)

The goal of this clinical trial is to test the feasibility, behavioral/neural mechanisms, and preliminary efficacy of "MINDfulness-based Substance Use Prevention Program," or "MINDS-UP", a novel substance use prevention meditation intervention for children and adolescents between the ages of 10 and 14. The main questions it aims to answer are: 1. Is MINDS-UP feasible and what is its preliminary efficacy? 2. Are MRI protocol and procedures feasible? An additional exploratory question is: Are there neural and psychopathological mechanisms through which MINDS-UP might work? Researchers will compare Sport - Prevention Plus Wellness (PPW) (an evidence based substance use prevention program) to Sport - Prevention Plus Wellness + MINDS-UP to examine the preliminary efficacy of MINDS-UP. Participants will * take assessment #1 * have 2 MRIs and take MINDS-UP, just take MINDS-UP or have a delayed start * take assessment #2 * take PPW, a single remote and research assistant-delivered 45-minute session * take assessment #3 * take assessment #4

Participants needed: 45
Trial details
Age: 10-14Biological sex: AllType: InterventionalSponsor: New York State Psychiatric InstituteUpdated: Apr 24, 2026
Eligibility criteria

Youth is ages 10-14 years on the day of screening [i.e., does not turn 15 before... [+2]

Has been diagnosed with or received treatment for one of the following mental he... [+2]