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Clinical Trials/NCT03212794
NCT03212794
Completed
Not Applicable

Initiating Substance Use Disorder Treatment for Hospitalized Opioid Use Disorder Patients.

Brigham and Women's Hospital1 site in 1 country29 target enrollmentFebruary 11, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Opioid-use Disorder
Sponsor
Brigham and Women's Hospital
Enrollment
29
Locations
1
Primary Endpoint
Treatment Retention
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this 24-week study is to evaluate the impact of recovery coach intervention on rates of treatment retention, illicit opioid use, and readmission among hospitalized patients newly initiated on buprenorphine or methadone compared to the control intervention.

Detailed Description

Patients with opioid use disorder (OUD) frequently utilize hospitals due to soft tissue infections and other conditions that require inpatient level of care. Prior studies have indicated that OUD patients are often amenable to initiating buprenorphine treatment and can be successfully linked to outpatient treatment. However, hospitalized OUD patients initiated on buprenorphine have much lower treatment retention rates at 6-months compared to OUD patients initiating treatment in the outpatient setting. As such, there is a great need to identify strategies to improve treatment retention in this patient population. There is a growing body of evidence for the benefits of recovery coaches, who provide peer-delivered support services in the community. Tracing their origin to mutual support groups to supplement traditional clinical services, recovery coaches are individuals with lived experience of recovery. Studies of recovery coaches have demonstrated greater treatment retention, reduced substance use, and reduced inpatient utilization. However, no prior studies have examined the impact of recovery coaches in improving medication-assisted treatment retention. As such, the aim of this 24-week study is to evaluate the impact of recovery coach intervention on rates of treatment retention, illicit opioid use, and readmission among hospitalized patients newly initiated on buprenorphine or methadone compared to the control intervention. Patients who are successfully initiated on buprenorphine or methadone, and are willing to engage in treatment after discharge, will be eligible to enroll. Assessments will be conducted at baseline, 4 weeks, 12 weeks, and 24 weeks.

Registry
clinicaltrials.gov
Start Date
February 11, 2019
End Date
December 30, 2021
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Joji Suzuki, MD

Director, Division of Addiction Psychiatry

Brigham and Women's Hospital

Eligibility Criteria

Inclusion Criteria

  • English speaking, adults aged 18-75
  • Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) diagnosis of opioid use disorder, severe, actively using illicit opioids until the time of hospitalization
  • Have a working telephone
  • Can identify at least 2 individuals who can act as points of contact following discharge from the hospital
  • Willing to engage in treatment (either a psychosocial treatment program AND/OR medication treatment with methadone or buprenorphine)

Exclusion Criteria

  • Liver function test \>3x upper normal limit
  • Psychotic disorder, active suicidality or homicidality
  • Condition likely to be terminal in 24 weeks such as cancer
  • Unable to perform consent due to mental status
  • Engaged in substance abuse treatment in the last month prior to admission

Outcomes

Primary Outcomes

Treatment Retention

Time Frame: 24 weeks after baseline

Primary outcome was retention in MOUD treatment at 6-months after discharge. If referred to programs affiliated with Brigham and Women's Hospital (BWH), the electronic health records were used to confirm treatment retention. Otherwise, retention was determined through self-report or confirmation with collateral contacts. If the electronic health record was not available for confirmation and the participant was lost to follow-up, the missing data was imputed as discontinuation of MOUD treatment.

Secondary Outcomes

  • Readmissions(24 weeks after baseline)
  • Days to Hospital Readmission(24 weeks after baseline)
  • Days to Treatment Discontinuation(24 weeks after baseline)

Study Sites (1)

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