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Search / Trial NCT06116266

Collaborative Care for Polysubstance Use in Primary Care Settings (Co-Care)

Launched by NYU LANGONE HEALTH · Oct 31, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

The Co-Care trial is studying a new approach to help adults who struggle with multiple substance use issues, particularly involving opioids, stimulants like cocaine and methamphetamine, and heavy alcohol use. The goal is to see if a collaborative care model, where different healthcare providers work together, can effectively reduce the amount of these substances people use. If you or a loved one is aged 18 or older, has a moderate to severe substance use disorder, and is currently using two or more substances, you might be eligible to participate.

Participants in this trial can expect to work closely with healthcare providers who will support them in their recovery journey. Eligible patients must be willing to engage in the study and provide informed consent. They should also have access to a reliable phone for communication. It's important to note that those currently receiving certain treatments for substance use disorders or who have recently started treatment may not be eligible. This trial is actively recruiting participants, so if you think you qualify, it could be a meaningful opportunity to get help.

Gender

ALL

Eligibility criteria

  • PCP Inclusion Criteria:
  • Licensed medical professional (MD, DO, NP, PA) who is able to prescribe controlled substances (Schedule III), or medical trainee meeting the requirements below.
  • Serves as a primary care provider to adult patients (18 years of age and over) of the study clinic(s) during direct patient care sessions.
  • Willing to be randomized to either of the study conditions. a. Medical trainees (physicians who are residents or fellows), are eligible if they have at least one continuity clinic session per week on average in the study clinic. Trainees must have plans to be working in a study clinic for approximately 8 months or longer. They must be able to provide prescriptions for controlled substances (Schedule III) either directly or through their preceptor(s).
  • Patient Inclusion Criteria:
  • The participant's PCP is enrolled in the study.
  • Age 18 years or older.
  • Spoken and written proficiency in language of study materials, as determined by patient self-report and research staff evaluation.
  • Moderate to severe substance use disorder for opioids, stimulants, and/or alcohol, (defined as meeting four or more DSM-5 criteria per substance as measured on the CIDI-adapted for DSM-5).
  • a) Patients having alcohol use disorder without an opioid or stimulant SUD are required to have current opioid or stimulant use, as measured on the TAPS tool or baseline monthly survey.
  • Current polysubstance use, defined as self-reported use of two or more substances of concern in the past 30 days, at least one of which is required to be an opioid or stimulant. Substances of concern include opioids (illicit opioids, nonmedical use of prescription opioids), stimulants (cocaine, methamphetamine), alcohol (heavy drinking defined as more than 5 for men and 4 for women drinks on a single occasion), and benzodiazepines (nonmedical use). Nonmedical use includes using prescription medications more than prescribed, or that were not prescribed to the individual taking them.
  • Patients must report on the baseline monthly survey use in the past 30 days of at least one substance at or above the following thresholds: \>10 days for opioids; \>10 days for alcohol heavy drinking; \>7 days for stimulants. These minimum thresholds reflect levels of use that are typical for individuals with moderate to severe SUD, and are lower for stimulants than for opioids and alcohol to reflect the different patterns of use that are observed in prior trials.
  • Access to a reliable cell phone or willing to accept a phone as part of the incentive for completing the baseline visit (as determined by patient self-report).
  • Able to provide sufficient contact information (minimum of one locator).
  • Willing and able to provide written informed consent.
  • PCP Exclusion Criteria:
  • Definite plan to resign from the clinic in the next eight months, per PCP self-report. Residents and fellows will need at least eight months before training completion to enroll.
  • Patient Exclusion Criteria:
  • Currently being treated with medication for OUD (MOUD), and do not have moderate to severe AUD or StUD
  • Initiated MOUD treatment (buprenorphine, methadone, or XR-NTX) within the 30 days prior to screening, per patient self-report. Because substance use may fall rapidly with the initiation of MOUD, patients who recently started MOUD may already be in the process of making changes to their substance use that are not attributable to the intervention.
  • a) Initiation is defined as starting a new MOUD treatment episode, after not receiving MOUD treatment in the prior 30 days
  • Initiated a SUD treatment program within the 30 days prior to screening, per patient self-report. Because substance use may fall rapidly with the initiation of a treatment program, patients who recently initiated treatment may already be making changes to their substance use that are not attributable to the intervention. SUD treatment program includes outpatient or residential programs for alcohol/drug treatment; does not include detox or short-term inpatient episodes (\<15 days), or peer support (e.g., 12-Step Program such as AA/NA, Smart Recovery)
  • a) Initiation is defined as starting a new treatment episode, after not being in a SUD treatment program in the prior 30 days
  • Pregnancy, as determined by patient self-report.
  • Are currently in jail, prison, or other overnight facility as required by court of law or have pending legal action that could prevent participation in study activities
  • Definite plan to leave the area or the clinical practice within the next six months, per patient self-report.
  • Other factors that may cause harm or increased risk to the participant or close contacts or preclude the patient's full adherence with or completion of the study (e.g. unstable/severe acute mental illness).

About Nyu Langone Health

NYU Langone Health is a premier academic medical center located in New York City, renowned for its commitment to advancing healthcare through innovative research and clinical excellence. As a leading sponsor of clinical trials, NYU Langone Health integrates cutting-edge scientific inquiry with patient-centered care, striving to develop new therapies and improve health outcomes across a wide range of medical conditions. The institution is dedicated to fostering collaboration among researchers, clinicians, and patients, ensuring rigorous adherence to ethical standards and regulatory guidelines in all clinical research initiatives. By leveraging its extensive resources and expertise, NYU Langone Health aims to contribute significantly to the advancement of medical knowledge and the enhancement of patient care.

Locations

Torrance, California, United States

New York, New York, United States

New York, New York, United States

Enterprise, Oregon, United States

Lancaster, Pennsylvania, United States

Houston, Texas, United States

Bellingham, Washington, United States

Madison, Wisconsin, United States

Patients applied

0 patients applied

Trial Officials

Jennifer McNeely, MD

Principal Investigator

NYU Langone Health

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported