NavSTAR Intervention for Opioid Use Disorder

(Philly NavSTAR Trial)

No longer recruiting at 1 trial location
KA
JG
Overseen ByJan Gryczynski, PhD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Friends Research Institute, Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 1 JurisdictionThis treatment is already approved in other countries

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores a new approach to help people with opioid use disorder (OUD) access treatment more effectively. It focuses on a service called NavSTAR, which guides patients through the healthcare system to overcome obstacles in obtaining necessary care. Initially, the trial will test NavSTAR with a small group in Philadelphia, then expand to a larger group to assess its potential for widespread and sustainable use. Participants should have moderate to severe OUD, reside in Philadelphia, and not have been in treatment recently. As an unphased trial, this study offers participants the chance to contribute to innovative solutions for improving OUD treatment access.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What prior data suggests that the NavSTAR intervention is safe for patients with opioid use disorder?

Research has shown that the NavSTAR program helps people with opioid use disorder. In a study involving 400 participants, NavSTAR not only increased the number of individuals starting treatment but also reduced hospital readmissions. The study also found it to be cost-effective.

While the study evaluated the program's effectiveness, it did not specifically address safety issues like side effects. However, its successful use by many suggests it is well-tolerated. As NavSTAR is a service model rather than a medication, it lacks the risks associated with drug treatments. This reduces the likelihood of direct side effects, making it generally safe for participants.12345

Why are researchers excited about this trial?

NavSTAR is unique because it tackles opioid use disorder with a comprehensive approach focusing on reducing barriers to care, rather than just treating symptoms. Unlike standard treatments that primarily rely on medications like methadone or buprenorphine, NavSTAR integrates motivational interventions with proactive support to address challenges in addiction, medical care, and basic needs. Researchers are excited because this method has the potential to improve long-term engagement in treatment services by addressing the root causes that often prevent individuals from accessing and sticking with their care plans.

What evidence suggests that the NavSTAR intervention is effective for opioid use disorder?

Studies have shown that NavSTAR, the treatment being tested in this trial, helps people with opioid use disorder. In a previous study with 400 participants, NavSTAR significantly increased the number of people starting treatment for this condition and reduced hospital readmissions. Additionally, NavSTAR proved to be cost-effective compared to usual treatments, meaning it works well and saves money. The evidence suggests NavSTAR can make a real difference in managing opioid use disorder.16789

Who Is on the Research Team?

KA

Karen Alexander, PhD

Principal Investigator

Friends Research Institute, Inc.

JG

Jan Gryczynski, MD

Principal Investigator

Friends Research Institute, Inc.

Are You a Good Fit for This Trial?

This trial is for individuals who have been hospitalized and are dealing with opioid use disorder. It aims to help those, especially from racial minority groups, access treatment post-hospitalization. The study will first involve a small group across four hospitals in Philadelphia before expanding.

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.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Pilot Testing

Conducting four short-duration, iterative pilot testing cycles in four hospitals to examine the Implementation Facilitation strategy for feasibility and acceptability

4 months
Multiple visits across 4 hospitals

Implementation

Large trial with 720 patient participants to implement NavSTAR and create a sustainable plan for post-discharge opioid agonist treatment

10 months

Follow-up

Participants are monitored for safety and effectiveness after treatment, including opioid agonist treatment initiation and other secondary outcomes

3 months

What Are the Treatments Tested in This Trial?

Interventions

  • NavSTAR (Philly adaptation)
Trial Overview The NavSTAR (Philly adaptation) intervention is being tested to see if it can improve entry into opioid use disorder treatment, reduce hospital readmissions, and be cost-effective. The trial involves engaging community and hospital partners to implement this patient navigation system.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: NavSTARExperimental Treatment1 Intervention

NavSTAR (Philly adaptation) is already approved in United States for the following indications:

🇺🇸
Approved in United States as NavSTAR for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

Friends Research Institute, Inc.

Lead Sponsor

Trials
60
Recruited
22,500+

Thomas Jefferson University

Collaborator

Trials
475
Recruited
189,000+

National Institute on Drug Abuse (NIDA)

Collaborator

Trials
2,658
Recruited
3,409,000+

Published Research Related to This Trial

A quality improvement initiative successfully implemented a program to initiate buprenorphine/naloxone treatment for opioid use disorder in 107 emergency departments across Alberta, leading to increased treatment initiation rates.
Most patients (67%) continued their opioid agonist prescriptions 180 days after their emergency department visit, and safety events were minimal, indicating that the program is both effective and safe for patients.
Buprenorphine/naloxone initiation and referral as a quality improvement intervention for patients who live with opioid use disorder: quantitative evaluation of provincial spread to 107 rural and urban Alberta emergency departments.Stone, KD., Scott, K., Holroyd, BR., et al.[2023]
The FDA-approved extended-release formulation of naltrexone, administered as a monthly injection, may improve adherence and retention rates in treating opioid dependence compared to the oral form, which has low compliance (less than 30%).
While naltrexone effectively reduces the rewarding effects of opioids to prevent relapse, there are safety concerns, including potential liver damage at high doses and risks of opioid overdose if individuals attempt to overcome the drug's antagonistic effects.
Naltrexone extended-release injection: an option for the management of opioid abuse.Taylor, R., Raffa, RB., Pergolizzi, JV.[2021]
Sustained release naltrexone (SRX) formulations, which can release the opioid antagonist for 1-7 months, have been shown to effectively reduce heroin use and have an acceptable safety profile based on multiple studies.
SRX not only helps in reducing opioid use but also appears to positively impact other areas such as reducing risky behaviors associated with blood-borne diseases, although more controlled studies are needed to fully understand its effectiveness compared to other treatments.
Injectable and implantable sustained release naltrexone in the treatment of opioid addiction.Kunøe, N., Lobmaier, P., Ngo, H., et al.[2021]

Citations

RePORT RePORTER - National Institutes of Health (NIH) |Our research team showed in a single-site randomized trial with 400 participants that NavSTAR significantly improved OAT entry, reduced readmissions, and was ...
Philly NavSTAR Implementation Trial | Clinical Research ...Our research team showed in a previous study with 400 participants that NavSTAR significantly increased entry into opioid use disorder treatment ...
NavSTAR Intervention for Opioid Use DisorderOur research team showed in a previous study with 400 participants that NavSTAR significantly increased entry into opioid use disorder treatment, reduced ...
Patient and navigator experiences with the opioid use ...People with opioid use disorder (OUD) discussed multiple treatment experiences. Barriers to treatment were lack of staff, limited hours, transportation, among ...
Philly NavSTAR Implementation Trial | MedPathOur research team showed in a previous study with 400 participants that NavSTAR significantly increased entry into opioid use disorder treatment, reduced ...
Polysubstance use and post-discharge mortality risk ...This study aimed to examine the association of comorbid cocaine, alcohol (binge drinking), and sedative use with mortality among hospitalized patients with ...
Navigation Services to Avoid Rehospitalization among ...This study was a parallel two-group randomized controlled trial that examined NavSTAR compared to TAU. Participants were 400 hospitalized ...
Bridging the Gap Between Hospital and Community-Based ...Lead researchers discuss the evaluation of NavSTAR, an intervention designed to reduce hospital readmissions by combining substance use ...
a secondary analysis of predictors from the NavSTAR TrialIn 2020, over 2 million adults in the U.S. met criteria for opioid use disorder (OUD) in the prior year [1], and nearly 70,000 overdose deaths ...
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