Implementing a patient navigation program for opioid use disorder treatment
Implementing a Patient Navigation Intervention Across a Health System to Address Treatment Entry Inequities
NA · Friends Research Institute, Inc. · NCT06634277
This study is trying out a new support program to help people with opioid use disorder get the treatment they need after leaving the hospital, especially focusing on helping those from racial minority groups.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 32 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Friends Research Institute, Inc. (other) |
| Locations | 2 sites (Philadelphia, Pennsylvania and 1 other locations) |
| Trial ID | NCT06634277 on ClinicalTrials.gov |
What this trial studies
This study aims to implement the NavSTAR patient navigation intervention for individuals with opioid use disorder (OUD) following hospitalization. By engaging community, hospital, and patient partners, the study seeks to address barriers to accessing treatment, particularly for racial minority groups. The intervention will be piloted in a health system to assess its feasibility, reach, and sustainability, building on previous findings that demonstrated its effectiveness in increasing treatment entry and reducing hospital readmissions. The study employs a hybrid implementation-effectiveness design to bridge the gap between research and practice.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 or older who meet the DSM-5 criteria for moderate to severe opioid use disorder.
Not a fit: Patients who have been enrolled in opioid use disorder treatment within 30 days prior to hospitalization or those residing outside the City of Philadelphia may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve access to opioid use disorder treatment and reduce overdose rates among vulnerable populations.
How similar studies have performed: Previous studies have shown success with similar patient navigation interventions, indicating potential for effective implementation in real-world settings.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria: 1. age 18 or older; 2. current DSM-5 criteria for moderate to severe OUD; 3. willing and able to provide informed consent in English. Exclusion criteria: 1. enrollment in OUD treatment 30-days prior to hospitalization; 2. residency outside the City of Philadelphia; 3. pregnancy; 4. planned discharge to a long-term inpatient care facility (e.g., hospice); 5. hospitalization for a suicide attempt.
Where this trial is running
Philadelphia, Pennsylvania and 1 other locations
- Jefferson Health — Philadelphia, Pennsylvania, United States (RECRUITING)
- Friends Research Institute — Philadelphia, Pennsylvania, United States (RECRUITING)
Study contacts
- Principal investigator: Karen Alexander, PhD — Friends Research Institute, Inc.
- Study coordinator: Karen Alexander, PhD
- Email: kalexander@friendsresearch.org
- Phone: 267-398-3560
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Opioid Use Disorder, patient navigation