Overdose Prevention Centers and Behavioral Health
Part of paid clinical trials in New York, New York.
- Sponsor
- NYU Langone Health
- Study ID
- NCT06236087
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Overdose
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Study Details
The aims of this study are: (Aim 1) Identify sources of heterogeneous impacts of opioid prevention center (OPC) use on non-fatal and fatal overdose risk among individuals with histories of polysubstance use (PSU); (Aim 2) Estimate the impact of OPC use on treated psychiatric events among clients with histories of PSU, and; (Aim 3) Assess the barriers and facilitators of integrating mental health services into existing syringe service and OPC delivery models.
Key Dates
- Start date
- Sep 1, 2026
- Status verified
- Feb 2026
- Primary completion
- Dec 31, 2026
- Completion
- Sep 30, 2027
Study Design
- Enrollment
- 500 participants (estimated)
Arms
- Arm: Aim 1 & 2 - DatasetFor Aims 1 and 2, an existing, de-identified dataset will be used for secondary analysis, including records for a maximum of 500 individuals. Aim 1 will use machine learning to identify sub-groups for whom OPC use is most and least protective of overdose risk. Identifying key intersectional groups across demographic (e.g., race/ethnicity, gender, and age), PSU factors (e.g., drug types and routes of administration), and socio-behavioral (e.g., mental health history, justice history, and homelessness) characteristics will inform targeted service delivery. Aim 2 will use epidemiological methods to estimate the association of OPC use with mental health services salient to PSU populations (e.g., hospitalization for depression, anxiety, and bipolar disorder). Measuring the association of OPC use with treated mental health outcomes for PSU-involved populations will foster an understanding of the impacts of OPCs on critical but unevaluated outcomes.
- Arm: Aim 3 - Harm Reduction StaffFor Aim 3, individuals employed at harm reduction programs in NYC will be enrolled for a one-time qualitative interview. Qualitative interviews will explore organizational (i.e., readiness, culture, and priorities), individual (i.e., attitudes and norms), and intervention (i.e., complexity and advantage) characteristics related to the integration of mental health and harm reduction services. Findings will inform efforts to scale ancillary mental health services high-risk PSU population.
Primary Outcome Measure
Incidence of Fatal Overdose [ Time Frame: Up to Month 12 ]
Central Contacts
- Bennett Allen, PhD, MPA646-501-3708
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| NYU Langone Health | New York | New York | 10016 | - |
Find similar trials in New York, NY
Related Studies
- Shelter HArm Reduction EvaluationRecruiting · NYU Langone Health · New York, New York
- Permanent Supportive Housing Overdose Prevention+ StudyNot Yet Recruiting · NYU Langone Health · New York, New York
- Emergency Medicine Peer Outreach Worker Engagement for RecoveryRecruiting · University of California, Los Angeles · Providence, Rhode Island
- A Universal Primary Care Based Intervention to Reduce Youth Overdose RiskRecruiting · Boston Medical Center · Boston, Massachusetts